Jump to content
RemedySpot.com

chelation research

Rate this topic


Guest guest

Recommended Posts

Guest guest

Hi

I'm new to the group and just wondered if anyone could point me to any

research that shows that chelation works in removing the mercury from

the brain and body, have there been any controlled studies. I am not

a parent just an interested professional who works with asd kids, and

admittedly am shocked by all of this. I am also considering this as a

treatment for myself due to mercury exposure from amalgam fillings.

Thanks

Link to comment
Share on other sites

Guest guest

In a message dated 09/05/2006 17:46:57 GMT Daylight Time, zyan@...

writes:

I'm new to the group and just wondered if anyone could point me to any

research that shows that chelation works in removing the mercury from

the brain and body, have there been any controlled studies. I am not

a parent just an interested professional who works with asd kids, and

admittedly am shocked by all of this. I am also considering this as a

treatment for myself due to mercury exposure from amalgam fillings.

_www.generationrescue.org_ (http://www.generationrescue.org)

_www.putchildrenfirst.org_ (http://www.putchildrenfirst.org)

No controlled studies but Ithink one underway with PhD, Paper by

Jeff Bradstreet showing increased excretion in ASD kids over controls with

DMSA.

Best place for reasearch

_http://home.earthlink.net/~moriam/_ (http://home.earthlink.net/~moriam/)

Good luck

Mandi in UK

_Treating Autism_ (http://www.treatingautism.com/)

Link to comment
Share on other sites

Guest guest

Welcome to the list. If you plan to chelate yourself you have to have the

amalgam fillings removed first by a mercury-free dentist using proper protocol.

Have you had a DDI hair test? It would show you if you have other toxic metals

in addition to the mercury. That's how I discovered that I had arsenic toxicity

in addition to my mercury poisoning.

S S

Hi<BR>

I'm new to the group and just wondered if anyone could point me to any <BR>

research that shows that chelation works in removing the mercury from <BR>

the brain and body, have there been any controlled studies.  I am not <BR>

a parent just an interested professional who works with asd kids, and <BR>

admittedly am shocked by all of this.  I am also considering this as a <BR>

treatment for myself due to mercury exposure from amalgam fillings.<BR>

<BR>

Thanks<BR>

_______________________________________________

Join Excite! - http://www.excite.com

The most personalized portal on the Web!

Link to comment
Share on other sites

Guest guest

Welcomed to the shocked crowd!! We all were at one time or another. If you

have mercury fillings and especially if you have had flu shots or other mercury

containing vaccines it would be good to look into your metal burden. There are

many diseases that are caused by mercury/metal poisoning. Alzheimer's in

particular has been thought to be caused by metals like mercury and aluminum.

They have a preference for fatty tissues and the brain is mostly fat thus they

tend to settle there.

Getting a hair test is a great first step. Getting those fillings removed is

also important. There is a particular protocol that is best for keeping the

amount of mercury you are exposed to at a minimum during the procedure.

The problem with research is that we have literally been hung out to dry by

the powers at be. Nobody will study chelation with ASD kids and it really is in

their best interests not to do the studies. If chelation works then it will

only take a second or two for people to realize the vaccines gave our kids

autism and not only will the entire vaccine program crumble in a matter of days

the lawyers will be circling like a bunch of sharks. The pharma companies that

make the vaccines, the lawmakers that mandated them and put them on the

recommended schedule, the doctors and everyone else involved is set up like

ducks for lawsuits. So instead of doing the moral and right thing we have

destroyed hundreds of thousands of children's lives as well as their families.

What we know about mercury and chelation...

1.Our kids were injected with a large amount of mercury.

2.Mercury is almost the most neurotoxic substance on earth.

3.Mercury poisoning and autism have virtually the same symptoms.

4.Autism rates jumped at the same time kids started to get several more Hg

containing shots, and has started to decline now that the Hg content is down.

5.Chelation has been around for a very long time. DMSA is a FDA approved drug

used to treat lead poisoning in children.

6.Chelation is said not to work by the authorities because they don't have

studies that say that is does. They also have no studies that say it doesn't.

7.Few people who do chelation properly report no benefit in their children.

Since being on this board the results have been amazing. People are talking all

the time about how well their kids are doing. Mine is one of them. We are

doing chelation and every round we do brings with it improvement.

8.Many of us have lab test results showing metal toxicity.

9.Many also have lab test results showing their kids dumping lots and I mean

lots of metals during chelation.

We are on our own with this. There are several different protocols out there

for metal removal. Since there are no good studies out there it is up to us to

find which protocols are helpful and which are harmful. With anything there is

a good and bad side.

Definitely keep doing research into this. I was shocked and amazed to find

all the information out here on the web about vaccines/mercury and autism. I

was provaccine until I learned better. The greatest lie out there though is

that the shots don't have anything to do with it because autism is just

diagnosed at that age and you can't blame shots for autism when they just

naturally occur at the same time. They only occur at the same time because one

causes the other and the fact that they occur at the same time is proof of that

actually if you look at the history of autism. Autism was first diagnosed

mostly in infants. That is why it was origionally called infantile autism. It

happened in about 1 in every 10,000 births and the babies were generally ASD at

birth. Very rare. So rare that when Bernard Shaw's son was diagnosed over 30

years ago he had never heard of autism and he was a PhD psychologist. His peds

doctor had never seen a case. That is rare. As the

vaccine program got going and more and more kids got more and more shots it was

at about the 18 month stage that their bodies just couldn't handle anymore and

started shutting down. Regressive autism like you have now only came about with

the vaccine program. Please someone/anyone correct me, I am going on little

sleep and memory here!!

What kind of professional are you if you don't mind me asking?

Welcome to our group, there are some amazing people here!!! Lots of kids

recovering from autism here!!

Also, you should check out the Generation Rescue website as well as the NVIC

websites. Those with thinktwice are my favorites.

zyansansom1974 <zyan@...> wrote:

Hi

I'm new to the group and just wondered if anyone could point me to any

research that shows that chelation works in removing the mercury from

the brain and body, have there been any controlled studies. I am not

a parent just an interested professional who works with asd kids, and

admittedly am shocked by all of this. I am also considering this as a

treatment for myself due to mercury exposure from amalgam fillings.

Thanks

=======================================================

Link to comment
Share on other sites

Guest guest

http://www.autismwebsite.com/ari/dan/scientificfoundations.htm

Binstock compiled this list.

Scientific Foundations of a DAN! Protocol

Binstock

Researcher in Developmental & Behavioral Neuroanatomy

binstock@...

P.O. Box 1788 Estes Park, CO 80517

View [Adobe pdf file] Binstock's mini-DAN! Power Point

presentation (Nov. 2004) - Auburn, Alabama.

Controversies: thimerosal and MMR – cites 1-36

Intestinal Pathologies – cites 37-65

vMV in PBMCs, as variant SSPE – cites 66-72

MMR: MV antibodies in autism– cites 73-77

vMV, MV impair immunity – cites 78-83

MV & Vitamin A – cites 84-97

Vitamin A & IgA, sIgA – cites 88b-88h

Autism, malnutrition, flora – cites 98-106

Gastrointestinal miscellany – cites 107-112

Glutathione – cites 113-125

Tylenol depletes GSH – cites 126-129

GSH & thimerosal – cites 130-134

Chorioamnionitis, fetal, placental – cites 135-142

Colic, cow's milk allergy in breast fed infants – cites 143-149

Chronic Diarrhea of Infancy – cites 150-153

Recurrent otitis & GSH– cites 154-160

Gluten hypersensitivity, bacteria – cites 161-171

Gluten neuropathologies – cites 172-176

Gluten immunologics, ataxia – cites 177-181

Chelation – cites 182-194

Viruses – cites 195-203

Probiotics – cites 204-213

Immune impairments in autism– cites 214-223

Methylcobalamin (mB12) – cites 224-239

Nutritional Therapy & Violent Behavior -- cite 240

Epileptiform pattern in autism – cites 241-246

Amino acids & epileptiform activity – cites 247- 253

Autism Treatment Evaluation Checklist (ATEC) - cite 254

New Autism Epidemiology Study - whole article free online – cite 255

Controversies: thimerosal and MMR – cites 1-36

1: SK et al. Thimerosal-containing vaccines and autistic

spectrum disorder: a critical review of published original data.

Pediatrics. 2004 Sep;114(3):793-804.

2: s N et al. Thimerosal exposure in infants and developmental

disorders: a retrospective cohort study in the United kingdom does

not support a causal association. Pediatrics. 2004 Sep;114(3):584-

91.

3: Heron J, Golding J; ALSPAC Study Team. Thimerosal exposure in

infants and developmental disorders: a prospective cohort study in

the United kingdom does not support a causal association.

Pediatrics. 2004 Sep;114(3):577-83.

4. Madsen KM et al. A population-based study of measles, mumps, and

rubella vaccination and autism. N Engl J Med. 2002 Nov 7;347

(19):1477-82.

5. Geier MR, Geier DA. Thimerosal does not belong in vaccines. 8

September 2004

http://pediatrics.aappublications.org/cgi/eletters/114/3/584

6. Carol Stott et al. MMR and Autism in Perspective: The Denmark

Story

http://www.jpands.org/vol9no3/stott.pdf

7. G.S. Goldman; F.E.Yazbak. An Investigation of the Association

Between MMR Vaccination and Autism in Denmark.

http://www.jpands.org/vol9no3/goldman.pdf

8a. CDC quote from p22: Bernard/Safeminds presentation to IOM, Oct

21, 2004

http://www.safeminds.org/iomvsd21oct04presentation.pdf

8b. Summary of CDC 1999 findings, p96-7 in: Neurodevelopmental

disorders following thimerosal-containing childhood vaccines...

Geier DA, Geier MR, in DAN! Conference Proceedings, Fall 2004, p95-

101.

In 1999, the CDC intiated study designed to review the medical

records of hundreds of thousands of children in the CDC's Vaccine

Safety Datalink (VSD). The VSD is a massive databse that tracks the

medical records of hundreds of thousands of patients belonging to

seven major health maintenance organizations.

" In the initial analysis of the VSD database conducted by Dr.

Verstraeten, [then] a CDC researcher, in the fall of 1999, showed

statistically significantly large increased risks for

neurodevelopmental disorders following additional doses of

thimerosal... The following are [sic] a brief sampling of some of

effects observed: "

autism = 7.62 (95% Confidence Interval (CI) = 1.84-31.5)

autism = 11.35 (95% CI = 2.70-47.76)

specific disorders of sleep of non-organic origin = 4.98 (95% CI =

1.55-15.94)

specific disorders of sleep of non-organic origin = 4.64 (95% CI =

1.12-19.25)

phase-disruption of 24-hour sleep-wake cycle = 53.64 (95% CI = 3.23-

892.10)

somnambulism or night terrors = 5.76 (95% CI = 1.38-24.05)

attention deficit without mention of hyperactivity = 6.38 (95% CI =

1.56-26.09)

attention deficit with mention of hyperactivity = 8.29 (95% CI =

2.03-33.89)

developmental speech or language disorder = 2.09 (95% CI = 1.08-

4.03)

other developmental speech or language delay = 2.32 (95% CI = 1.20-

4.48)

unspecified delay in development = 2.08 (95% CI = 1.03-4.19)

[the above data] among children receiving > 25 micrograms

ethylmercury from thimerosal at age 1 month in comparison to

children receiving 0 micrograms of ethylmercury at age 1 month;

attention deficit disorder = 2.88 (95% CI = 1.05-7.88) and

attention deficit disorder = 2.84 (95% CI = 1.03-7.85), and

coordination disorder = 18.26 (95% CI = 5.65-59.01)

among children receiving > 75 micrograms of ethylmercury from

thimerosal in comparison to children receiving < 12.5 microgram from

thimerosal at age 3 months; and

autism = 2.15 (95% CI = 1.04-4.43) and

among children receiving increases of 7.5-10 micrograms of

thimerosal over 1 month, in comparison to children receiving less

than 5 micrograms of ethylmercury from thimerosal over 1 month [9-

10].

" Additionally, studies were conducted in 2000 by CDC to evaluate the

dose-response effects of thimerosal on childhood neurodevelopmental

disorders based upon evaluation of the VSD database [11]. It was

found that there were statistically significant relationships

between increasing exposures to thimerosal and the following

outcomes, including:

(1) for two months of age, an unspecified developmental delay, which

has its own ICD-9 code.

(2) Exposure at three months of age, Tics.

(3) Exposure at six months of age, language and speech delays, which

are two separate ICD-9 codes.

(4) Exposure at one, three and six months of age, the entire

category of neurodevelopmental delays, which includes all of these

plus a number of other disorders (i.e., including autism). "

[9.] Email from Verstraeten to and

Destefano. Nov 29, 1999. Obtained under FOIA by SafeMinds.

[10.] Email from Verstraeten to and

Destefano.Dec 17, 1999. Obtained under FOIA by SafeMinds.

8c. The Truth behind the Vaccine Coverup. Blaylock MD. Sep

12 2004

http://sydney.indymedia.org/front.php3?

article_id=45874 & group=webcast

Excerpt: " It all started when a friend of mind sent me a copy of a

letter from Congressman Weldon, M.D. to the director of the

CDC, Dr L. Gerberding, in which he alludes to a study by a

Doctor Verstraeten, then representing the CDC, on the

connection between infant exposure to thimerosal-containing vaccines

and neurodevelopmental

injury. In this shocking letter Congressman Weldon referrers to Dr.

Verstraeten's study which looked at the data from the Vaccine Safety

Datalink and found a significant correlation between thimerosal

exposure via vaccines and several neurodevelopmental disorders

including tics, speech and language delays, and possibly to ADD.

" Congressman Weldon questions the CDC director as to why, following

this meeting, Dr. Verstraeten published his results, almost four

years later, in the journal Pediatrics to show just the opposite,

that is, that there was no correlation to any neurodevelopmental

problems related to thimerosal exposure in infants… "

8d. Original in-house CDC study is online. Verstraeten et al 2000,

unpublished; obtained via FOIA

http://factsformedia.com/factsformedia/thimerosalstudy.pdf

9a. Excerpts from CDC's in-house conference: Thimerosal sequelae

http://www.nationalautismassociation.org/library/IOM%20Simpsonwood%

20in%20bold.pdf

9b. Blaylock R, MD. The thimerosal coverup – a thorough delineation

of CDC, FDA knowledge about thimerosal circa 1999.

http://sydney.indymedia.org/front.php3?article_id=45874 & group=webcast

10a. House Subcommittee Hearing transcripts: Truth Revealed: New

Scientific Discoveries Regarding Mercury in Medicine and Autism.

September 08, 2004

http://reform.house.gov/WHR/Hearings/EventSingle.aspx?EventID=1311

10b. Testimony of Lyn Redwood, RN, MSN; President; Safeminds

http://reform.house.gov/UploadedFiles/Testimony Redwood.pdf

10c. Analysis and critique of the CDC's handling of the thimerosal

exposure assessment based on Vaccine Safety Datalink (VSD)

information. Safeminds, 2003.

http://www.momsonamissionforautism.org/index/VSD.SafeMinds.critique.p

df

10d. NoMercury.org – an information resource about thimerosal

http://www.nomercury.org/

11. Verstraeten T, RL, DeStefano F et al. Safety of

thimerosal-containing vaccines: a two-phased study of computerized

health maintenance organization databases. Pediatrics. 2003 Nov;112

(5):1039-48. Erratum in: Pediatrics. 2004 Jan;113(1):184.

12. Geier MR, Geier DA. Neurodevelopmental disorders after

thimerosal-containing vaccines: a brief communication. Exp Biol Med

2003 228(6):660-4 PMID 12773696

" We were initially highly skeptical that differences in the

concentrations of thimerosal in vaccines would have any effect on

the incidence rate of neurodevelopmental disorders after childhood

immunization. This study presents the first epidemiologic evidence,

based upon tens of millions of doses of vaccine administered in the

United States, that associates increasing thimerosal from vaccines

with neurodevelopmental disorders. "

13. Geier DA, Geier MR. An assessment of the impact of thimerosal on

childhood neurodevelopmental disorders. Pediatr Rehabil. 2003 6

(2):97-102 PMID 14534046

" The [thimerosal] dose-response curves showed increases in odds

ratios of neurodevelopmental disorders from both the VAERS and US

Department of Education data closely linearly correlated with

increasing doses of mercury from thimerosal-containing childhood

vaccines and that for overall odds ratios statistical significance

was achieved. Similar slopes and linear regression coefficients for

autism odds ratios in VAERS and the US Department of Education data

help to mutually validate each other. "

14. Geier DA, Geier MR. A comparative evaluation of the effects of

MMR immunization and mercury doses from thimerosal-containing

childhood vaccines on the population prevalence of autism. Med Sci

Monit. 2004 Mar;10(3):PI33-9. Epub 2004 Mar 01.

15. Geier MR, Geier DA. Autism and thimerosal-containing vaccines:

analysis of the Vaccine Adverse Events Reporting System (VAERS). IOM

presentation, Feb 9, 2004.

Slides: http://www.iom.edu/view.asp?id=18392

Audio: http://www.iom.edu/view.asp?id=19120

16. Geier & Geier. Parents' worries about thimerosal in vaccines are

well founded!

http://pediatrics.aappublications.org/cgi/eletters/112/6/1394

[An excellent summary & rebuttal of pro-thimerosal articles.]

17. Baskin DS et al. Thimerosal induces DNA breaks, caspase-3

activation, membrane damage, and cell death in cultured human

neurons and fibroblasts. Toxicol Sci. 2003 Aug;74(2):361-8. Epub

2003 May 28. PMID: 12773768

18. Baskin, M.D. Relation of Neurotoxic Effects of Thimerosal

to Autism. IOM presentation, Feb 9, 2004. Audio only:

http://www.iom.edu/view.asp?id=19124

19. Pichichero ME et al. Mercury concentrations and metabolism in

infants receiving vaccines containing thiomersal: a descriptive

study. Lancet. 2002 30;360(9347):1737-41. PMID 12480426

" Interpretation: Administration of vaccines containing thiomersal

does not seem to raise blood concentrations of mercury above safe

values in infants. " [but see cite 20]

20. Waly M et al. Activation of methionine synthase by insulin-like

growth factor-1 and dopamine: a target for neurodevelopmental toxins

and thimerosal. Mol Psychiatry. 2004 Apr;9(4):358-70. PMID:

14745455

" Our findings outline a novel growth factor signaling pathway that

regulates MS activity and thereby modulates methylation reactions,

including DNA methylation. The potent inhibition of this pathway by

ethanol, lead, mercury [at nanomolar levels described by Pichichero

et al), aluminum and thimerosal suggests that it may be an important

target of neurodevelopmental toxins. "

21. C. Deth, Ph.D. Effects of Mercury on Methionine

Synthase: Implications for Disordered Methylation in Autism DAN!

2003 Philadelphia

http://64.202.182.52/powerpoint/dan2003/Deth.htm

22a. Mady Hornig, M.D Etiologic factors and pathogenesis of autism:

evidence from clinical studies and animal models. IOM presentation

Feb 9 2004 Audio only: http://www.iom.edu/view.asp?id=19108

22b. Mady Hornig, PhD: Testimony to House Subcommittee Sept 8 2004

http://reform.house.gov/UploadedFiles/Testimony Hornig.pdf

23. Westphal GA et al. Homozygous gene deletions of the glutathione

S-transferases M1 and T1 are associated with thimerosal

sensitization. Int Arch Occup Environ Health. 2000 Aug;73(6):384-8.

PMID: 11007341

24: Muller M et al. Inhibition of the human erythrocytic

glutathione-S-transferase T1 (GST T1) by thimerosal. Int J Hyg

Environ Health. 2001 Jul;203(5-6):479-81. PMID: 11556154

25. Westphal GA et al. Thimerosal induces micronuclei in the

cytochalasin B block micronucleus test with human lymphocytes. Arch

Toxicol. 2003 Jan;77(1):50-5. Epub 2002 Nov 06. PMID: 12491041

26. Havarinasab S et al. Dose-response study of thimerosal-induced

murine systemic autoimmunity. Toxicol Appl Pharmacol. 2004 194

(2):169-79. PMID: 14736497

" The autoimmune syndrome induced by thimerosal is different from the

weaker and more restricted autoimmune reaction observed after

treatment with an equipotent dose of methylmercury. "

27. Vojdani A, Pangborn JB et al. Infections, toxic chemicals and

dietary peptides binding to lymphocyte receptors and tissue enzymes

are major instigators of autoimmunity in autism. Int J Immunopathol

Pharmacol. 2003 Sep-Dec;16(3):189-99. PMID: 14611720

28. Holmes AS, Blaxill MF, Haley BE. Reduced levels of mercury in

first baby haircuts of autistic children. Int J Toxicol. 2003 Jul-

Aug;22(4):277-85. PMID: 12933322

" Hair mercury levels in the autistic group were 0.47 ppm versus 3.63

ppm in controls, a significant difference. The mothers in the

autistic group had significantly higher levels of mercury exposure

through Rho D immunoglobulin injections and amalgam fillings than

control mothers. Within the autistic group, hair mercury levels

varied significantly across mildly, moderately, and severely

autistic children, with mean group levels of 0.79, 0.46, and 0.21

ppm, respectively. "

29. Boyd Haley, Ph.D. Reduced Levels of Mercury in First Baby

Haircuts of Autistic Children. IOM presentation, Feb 9 2004.

Slides: http://www.iom.edu/view.asp?id=18394

Audio: http://www.iom.edu/view.asp?id=19128

30: Boyd Haley, Ph.D. Nucleotides and Mercury DAN! 2003 Philadelphia

http://64.202.182.52/powerpoint/dan2003/Haley.htm

31. L-W. Hu et al. " Neutron Activation Analysis of Hair Samples for

the Identification of Autism " , Transactions of the American Nuclear

Society, Vol. 89, November 16-20, 2003.

32. Bernard S, Enayati A, Redwood L, H, Binstock T. Autism: a

novel form of mercury poisoning. Med Hypotheses. 2001 Apr;56(4):462-

71. PMID: 11339848

33. Bernard S, Enayati A, H, Binstock T, Redwood L. The role

of mercury in the pathogenesis of autism. Mol Psychiatry. 2002;7

Suppl 2:S42-3. PMID: 12142947

34. Excerpts from CDC's in-house conference: Thimerosal sequelae

http://www.nationalautismassociation.org/library/IOM%20Simpsonwood%

20in%20bold.pdf

35. Congressman, Dr. Weldon's letter to the CDC director, available

at:

http://momsonamissionforautism.org/Autism_Central/Dr_Weldon_Responds.

shtml

36a. IOM presentation of Congressman Dave Weldon, M.D.

http://www.nationalautismassociation.org/pdf/Weldon.pdf

36b. Doctors must prescribe without all the facts. Dr. Darshak

Sanghavi, Children's Hospital and Harvard Medical School.

sanghavi@... October 12, 2004

http://www.boston.com/news/globe/health_science/articles/2004/10/12/d

octors_must_prescribe_without_all_the_facts/

Intestinal pathologies

37. D'Eufemia P et al. Abnormal intestinal permeability in children

with autism. Acta Paediatr. 1996 Sep;85(9):1076-9. PMID: 8888921

" We determined the occurrence of gut mucosal damage using the

intestinal permeability test in 21 autistic children who had no

clinical and laboratory findings consistent with known intestinal

disorders. An altered intestinal permeability was found in 9 of the

21 (43%) autistic patients, but in none of the 40 controls. "

38. Reichelt KL, Knivsberg AM. Can the pathophysiology of autism be

explained by the nature of the discovered urine peptides? Nutr

Neurosci. 2003 Feb;6(1):19-28. PMID: 12608733

39. Mercer ME, Holder MD. Food cravings, endogenous opioid peptides,

and food intake: a review. Appetite. 1997 Dec;29(3):325-52. PMID:

9468764

40a. Lucarelli S et al. Food allergy and infantile autism.

Panminerva Med. 1995 Sep;37(3):137-41. PMID: 8869369

" The aim of the present study has been to verify the efficacy of a

cow's milk free diet (or other foods which gave a positive result

after a skin test) in 36 autistic patients. We also looked for

immunological signs of food allergy in autistic patients on a free

choice diet. We noticed a marked improvement in the behavioural

symptoms of patients after a period of 8 weeks on an elimination

diet and we found high levels of IgA antigen specific antibodies for

casein, lactalbumin and beta-lactoglobulin and IgG and IgM for

casein. The levels of these antibodies were significantly higher

than those of a control group which consisted of 20 healthy

children. "

40b. Iacono G et al. Chronic constipation as a symptom of cow milk

allergy. J Pediatr. 1995 Jan;126(1):34-9. PMID: 7815220

" Twenty-seven consecutive infants (mean age, 20.6 months) with

chronic " idiopathic " constipation were studied to investigate the

possible relation between constipation and cow milk protein allergy

(CMPA). The infants were initially observed on an unrestricted diet,

and the number of stools per day was recorded. Subsequently the

infants were put on a diet free of cow milk protein (CMP) for two

periods of 1 month each, separated by two challenges with CMP.

During the CMP-free diet, there was a resolution of symptoms in 21

patients; during the two consecutive challenges, constipation

reappeared within 48 to 72 hours. In another six patients the CMP-

free diet did not lead to improvement of constipation. Only four of

the patients who improved on the CMP-free diet had concomitant

symptoms of suspected CMPA, but a medical history of CMPA was found

in 15 of the 21 patients cured and in only one of the six patients

whose condition had not improved (p < 0.05); in addition, in 15 of

the 21 cured patients, results of one or more laboratory tests

(specific IgE, IgG, anti-beta-lactoglobulin, circulating

eosinophils) were positive at the time of diagnosis, indicating

hypersensitivity, compared with one of the six patients whose

condition did not improve (p < 0.05). The endoscopic and histologic

findings at the time of diagnosis showed proctitis with monocytic

infiltration in two patients cured with the CMP-free diet; after 1

month on this diet, they were completely normal. We conclude that

constipation in infants may have an allergic pathogenesis. "

40c. Iacono G et al. Intolerance of cow's milk and chronic

constipation in children. N Engl J Med. 1998 Oct 15;339(16):1100-

4. PMID: 9770556

BACKGROUND: Chronic diarrhea is the most common gastrointestinal

symptom of intolerance of cow's milk among children. On the basis of

a prior open study, we hypothesized that intolerance of cow's milk

can also cause severe perianal lesions with pain on defecation and

consequent constipation in young children. METHODS: We performed a

double-blind, crossover study comparing cow's milk with soy milk in

65 children (age range, 11 to 72 months) with chronic constipation

(defined as having one bowel movement every 3 to 15 days). All had

been referred to a pediatric gastroenterology clinic and had

previously been treated with laxatives without success; 49 had anal

fissures and perianal erythema or edema. After 15 days of

observation, the patients received cow's milk or soy milk for two

weeks. After a one-week washout period, the feedings were reversed.

A response was defined as eight or more bowel movements during a

treatment period. RESULTS: Forty-four of the 65 children (68

percent) had a response while receiving soy milk. Anal fissures and

pain with defecation resolved. None of the children who received

cow's milk had a response. In all 44 children with a response, the

response was confirmed with a double-blind challenge with cow's

milk. Children with a response had a higher frequency of coexistent

rhinitis, dermatitis, or bronchospasm than those with no response

(11 of 44 children vs. 1 of 21, P=0.05); they were also more likely

to have anal fissures and erythema or edema at base line (40 of 44

vs. 9 of 21, P<0.001), evidence of inflammation of the rectal mucosa

on biopsy (26 of 44 vs. 5 of 21, P=0.008), and signs of

hypersensitivity, such as specific IgE antibodies to cow's-milk

antigens (31 of 44 vs. 4 of 21, P<0.001). CONCLUSIONS: In young

children, chronic constipation can be a manifestation of intolerance

of cow's milk.

41. Arnold GL et al. Plasma amino acids profiles in children with

autism: potential risk of nutritional deficiencies. J Autism Dev

Disord 2003 33(4):449-54. PMID: 12959424

" No amino acid profile specific to autism was identified. However,

children with autism had more essential amino acid deficiencies

consistent with poor protein nutrition than an age/gender matched

control group. There was a trend for children with autism who were

on restricted diets to have an increased prevalence of essential

amino acid deficiencies and lower plasma levels of essential acids

including the neurotransmitter precursors tyrosine and tryptophan

than both controls and children with autism on unrestricted diets. "

42. Chauhan V et al. Alteration in amino-glycerophospholipids

levels in the plasma of children with autism: a potential

biochemical diagnostic marker. Life Sci 2004 Feb 13;74(13):1635-

43. PMID: 14738907

" the levels of AGP [amino-glycerophospholipids] were found to be

significantly increased in the plasma of children with autism as

compared to their non-autistic normal siblings. "

43. Knivsber AM et al. Reports on dietary intervention in autistic

disorders. Nutr Neurosci. 2001;4(1):25-37. PMID: 11842874

" …Gluten and/or casein free diet has been implemented to reduce

autistic behaviour, in addition to special education, since early in

the eighties. Over the last twelve years various studies on this

dietary intervention have been published in addition to anecdotal,

parental reports. The scientific studies include both groups of

participants as well as single cases, and beneficial results are

reported in all, but one study. While some studies are based on

urinary peptide abnormalities, others are not. The reported results

are, however, more or less identical; reduction of autistic

behaviour, increased social and communicative skills, and

reappearance of autistic traits after the diet has been broken. "

44. Karyn Seroussi -- Dietary Intervention for Autism DAN! 2003

Philadelphia

http://64.202.182.52/powerpoint/dan2003/KarynSeroussi.htm

45. ARI's Parent Ratings Data

http://www.autismresearchinstitute.com/treatment/form34q.htm

http://www.autismresearchinstitute.com/treatment/form34q.pdf

46: Wakefield AJ et al. Ileal-lymphoid-nodular hyperplasia, non-

specific colitis, and pervasive developmental disorder in children.

Lancet. 1998 28;351(9103):637-41. PMID: 9500320

47: Ashwood P et al. Intestinal lymphocyte populations in children

with regressive autism: evidence for extensive mucosal

immunopathology. J Clin Immunol. 2003 Nov;23(6):504-17. PMID:

15031638

" At all sites, CD3(+) and CD3(+)CD8(+) IEL as well as CD3(+) LPL

were significantly increased in affected children compared with

developmentally normal noninflamed control groups (p<0.01) reaching

levels similar to inflamed controls. In addition, two populations--

CD3(+)CD4(+) IEL and LP CD19(+) B cells--were significantly

increased in affected children compared with both noninflamed and

inflamed control groups including IBD, at all sites examined

(p<0.01). Histologically there was a prominent mucosal eosinophil

infiltrate in affected children that was significantly lower in

those on a gluten- and casein-free diet, although lymphocyte

populations were not influenced by diet.The data provide further

evidence of a pan-enteric mucosal immunopathology in children with

regressive autism that is apparently distinct from other

inflammatory bowel diseases. "

48: Wakefield AJ. Enterocolitis, autism and measles virus. Mol

Psychiatry. 2002;7 Suppl 2:S44-6. PMID: 12142948

49: Wakefield AJ. The gut-brain axis in childhood developmental

disorders. J Pediatr Gastroenterol Nutr. 2002 May-Jun;34 Suppl 1:S14-

7. PMID: 12082381

50. Binstock T. Anterior insular cortex: linking intestinal

pathology and brain function in autism-spectrum subgroups. Med

Hypotheses 2001 57(6):714-7. PMID: 11918432

" Numerous parents and some physicians report that an autistic

child's attention and language improve in response to treatments

which eliminate certain dietary antigens and/or which improve

intestinal health. For at least some autism-spectrum children, the

link between intestinal pathology, attention, and language may

derive from shared neuroanatomic pathways within the anterior

insular cortex (aIC); from a neurotrophic virus such as herpes

simplex (HSV) migrating within afferents to the insular cortex;

and/or from synaptic exhaustion in the aIC as induced by chronically

inappropriate neuronal activity in the enteric nervous system and/or

its vagal efferents. "

51: Torrente F et al. Small intestinal enteropathy with epithelial

IgG and complement deposition in children with regressive autism.

Mol Psychiatry. 2002;7(4):375-82, 334.

PMID: 11986981

" Most strikingly, IgG deposition was seen on the basolateral

epithelial surface in 23/25 autistic children, co-localising with

complement C1q. This was not seen in the other conditions. These

findings demonstrate a novel form of enteropathy in autistic

children, in which increases in mucosal lymphocyte density and crypt

cell proliferation occur with epithelial IgG deposition. The

features are suggestive of an autoimmune lesion. "

52. Uhlmann V et al. Potential viral pathogenic mechanism for new

variant inflammatory bowel disease. Mol Pathol. 2002 Apr;55(2):84-

90. PMID: 11950955

" AIMS: A new form of inflammatory bowel disease (ileocolonic

lymphonodular hyperplasia) has been described in a cohort of

children with developmental disorder. This study investigates the

presence of persistent measles virus in the intestinal tissue of

these patients (new variant inflammatory bowel disease) and a series

of controls by molecular analysis… RESULTS: Seventy five of 91

patients with a histologically confirmed diagnosis of ileal

lymphonodular hyperplasia and enterocolitis were positive for

measles virus in their intestinal tissue compared with five of 70

control patients. Measles virus was identified within the follicular

dendritic cells and some lymphocytes in foci of reactive follicular

hyperplasia. The copy number of measles virus ranged from one to

300,00 copies/ng total RNA. CONCLUSIONS: The data confirm an

association between the presence of measles virus and gut pathology

in children with developmental disorder. "

53. Wakefield AJ et al. Review article: the concept of entero-

colonic encephalopathy, autism and opioid receptor ligands.Aliment

Pharmacol Ther 2002 16(4):663-74. PMID 11929383

54. Furlano RI et al. Colonic CD8 and gamma delta T-cell

infiltration with epithelial damage in children with autism. J

Pediatr. 2001 Mar;138(3):366-72. PMID: 11241044

" OBJECTIVES: We have reported colitis with ileal lymphoid nodular

hyperplasia (LNH) in children with regressive autism. The aims of

this study were to characterize this lesion and determine whether

LNH is specific for autism. METHODS: Ileo-colonoscopy was performed

in 21 consecutively evaluated children with autistic spectrum

disorders and bowel symptoms. Blinded comparison was made with 8

children with histologically normal ileum and colon, 10

developmentally normal children with ileal LNH, 15 with Crohn's

disease, and 14 with ulcerative colitis. Immunohistochemistry was

performed for cell lineage and functional markers, and

histochemistry was performed for glycosaminoglycans and basement

membrane thickness. RESULTS: Histology demonstrated lymphocytic

colitis in the autistic children, less severe than classical

inflammatory bowel disease. However, basement membrane thickness and

mucosal gamma delta cell density were significantly increased above

those of all other groups including patients with inflammatory bowel

disease. CD8(+) density and intraepithelial lymphocyte numbers were

higher than those in the Crohn's disease, LNH, and normal control

groups; and CD3 and plasma cell density and crypt proliferation were

higher than those in normal and LNH control groups. Epithelial, but

not lamina propria, glycosaminoglycans were disrupted. However, the

epithelium was HLA-DR(-), suggesting a predominantly T(H)2 response.

INTERPRETATION: Immunohistochemistry confirms a distinct lymphocytic

colitis in autistic spectrum disorders in which the epithelium

appears particularly affected. This is consistent with increasing

evidence for gut epithelial dysfunction in autism. "

55. O'Leary JJ et al. Measles virus and autism. Lancet. 2000 Aug

26;356(9231):772. PMID: 11085720

56. Wakefield AJ et al. Enterocolitis in children with

developmental disorders. Am J Gastroenterol. 2000 Sep;95(9):2285-95.

PMID: 11007230

" OBJECTIVE: Intestinal pathology, i.e., ileocolonic lymphoid nodular

hyperplasia (LNH) and mucosal inflammation, has been described in

children with developmental disorders. This study describes some of

the endoscopic and pathological characteristics in a group of

children with developmental disorders (affected children) that are

associated with behavioral regression and bowel symptoms, and

compares them with pediatric controls. METHODS: Ileocolonoscopy and

biopsy were performed on 60 affected children (median age 6 yr,

range 3-16; 53 male). Developmental diagnoses were autism (50

patients), Asperger's syndrome (five), disintegrative disorder

(two), attention deficit hyperactivity disorder (ADHD) (one),

schizophrenia (one), and dyslexia (one). Severity of ileal LNH was

graded (0-3) in both affected children and 37 developmentally normal

controls (median age 11 yr, range 2-13 yr) who were investigated for

possible inflammatory bowel disease (IBD). Tissue sections were

reviewed by three pathologists and scored on a standard proforma.

Data were compared with ileocolonic biopsies from 22 histologically

normal children (controls) and 20 children with ulcerative colitis

(UC), scored in an identical manner. Gut pathogens were sought

routinely. RESULTS: Ileal LNH was present in 54 of 58 (93%) affected

children and in five of 35 (14.3%) controls (p < 0.001). Colonic LNH

was present in 18 of 60 (30%) affected children and in two of 37

(5.4%) controls (p < 0.01). Histologically, reactive follicular

hyperplasia was present in 46 of 52 (88.5%) ileal biopsies from

affected children and in four of 14 (29%) with UC, but not in non-

IBD controls (p < 0.01). Active ileitis was present in four of 51

(8%) affected children but not in controls. Chronic colitis was

identified in 53 of 60 (88%) affected children compared with one of

22 (4.5%) controls and in 20 of 20 (100%) with UC. Scores of

frequency and severity of inflammation were significantly greater in

both affected children and those with UC, compared with controls (p

< 0.001). CONCLUSIONS: A new variant of inflammatory bowel disease

is present in this group of children with developmental disorders. "

60. Wakefield AJ, Montgomery SM. Autism, viral infection and measles-

mumps-rubella vaccination. Isr Med Assoc J. 1999 Nov;1(3):183-7.

PMID: 10731332

61. Wakefield AJ. MMR vaccination and autism. Lancet. 1999 Sep

11;354(9182):949-50. PMID: 10489978

62a. Horvath K et al. Gastrointestinal abnormalities in children

with autistic disorder. J Pediatr. 1999 Nov;135(5):559-63. PMID:

10547242

" OBJECTIVES: Our aim was to evaluate the structure and function of

the upper gastrointestinal tract in a group of patients with autism

who had gastrointestinal symptoms. STUDY DESIGN: Thirty-six children

(age: 5.7 +/- 2 years, mean +/- SD) with autistic disorder underwent

upper gastrointestinal endoscopy with biopsies, intestinal and

pancreatic enzyme analyses, and bacterial and fungal cultures. The

most frequent gastrointestinal complaints were chronic diarrhea,

gaseousness, and abdominal discomfort and distension. RESULTS:

Histologic examination in these 36 children revealed grade I or II

reflux esophagitis in 25 (69.4%), chronic gastritis in 15, and

chronic duodenitis in 24. The number of Paneth's cells in the

duodenal crypts was significantly elevated in autistic children

compared with non-autistic control subjects. Low intestinal

carbohydrate digestive enzyme activity was reported in 21 children

(58.3%), although there was no abnormality found in pancreatic

function… CONCLUSIONS: Unrecognized gastrointestinal disorders,

especially reflux esophagitis and disaccharide malabsorption, may

contribute to the behavioral problems of the non-verbal autistic

patients… "

62b. Horvath K, Perman JA. Autism and gastrointestinal symptoms.

Curr Gastroenterol Rep. 2002 Jun;4(3):251-8. PMID: 12010627

63. Horvath K, Perman JA. Autistic disorder and gastrointestinal

disease. Curr Opin Pediatr. 2002 Oct;14(5):583-7. PMID: 12352252

" High prevalence of histologic abnormalities in the esophagus,

stomach, small intestine and colon, and dysfunction of liver

conjugation capacity and intestinal permeability were reported.

Three surveys conducted in the United States described high

prevalence of gastrointestinal symptoms in children with autistic

disorder. Treatment of the digestive problems may have positive

effects on their behavior. "

64. Quigley EM, Hurley D. Autism and the gastrointestinal tract. Am

J Gastroenterol. 2000 Sep;95(9):2154-6. PMID: 11007210

65. Tim Buie, M.D. Presentation at 2003 DAN!, Philadelphia.

http://64.202.182.52/powerpoint/dan2003/Buie.htm

vMV in PBMCs, as variant SSPE

66. Kawashima H et al. Detection and sequencing of measles virus

from peripheral mononuclear cells from patients with inflammatory

bowel disease and autism. Dig Dis Sci. 2000 Apr;45(4):723-9. PMID

10759242

" One of eight patients with Crohn disease, one of three patients

with ulcerative colitis, and three of nine children with autism,

were positive. Controls were all negative. The sequences obtained

from the patients with Crohn's disease shared the characteristics

with wild-strain virus. The sequences obtained from the patients

with ulcerative colitis and children with autism were consistent

with being vaccine strains. The results were concordant with the

exposure history of the patients. Persistence of measles virus was

confirmed in PBMC in some patients with chronic intestinal

inflammation. "

67. Jeff Bradstreet, M.D. A Case-control Study of Mercury Burden in

Children with Autistic Disorders and Measles Virus Genomic RNA in

Cerebrospinal Fluid in Children with Regressive Autism. IOM

presentation, Feb 9, 2004.

Slides: http://www.iom.edu/view.asp?id=18578

Audio: http://www.iom.edu/view.asp?id=19130

68. 48a: Valsamakis A et al. Altered virulence of vaccine strains of

measles virus after prolonged replication in human tissue. J Virol.

1999 73(10): 8791-7. PMID 10482633

http://jvi.asm.org/cgi/reprint/73/10/8791.pdf

69. Binstock T. Intra-monocyte pathogens delineate autism subgroups.

Med Hypotheses. 2001 Apr;56(4):523-31. PMID 11339860

70. Garg RK. Subacute sclerosing panencephalitis.Postgrad Med J.

2002 Feb;78(916):63-70. PMID 11807185.

71. Neuroprogressive disease of post-infectious origin: a review of

a resurging subacute sclerosing panencephalitis (SSPE). Ment Retard

Dev Disabil Res Rev. 2001;7(3):217-25. PMID: 11553938

72. Gascon GG. Subacute sclerosing panencephalitis. Semin Pediatr

Neurol. 1996 Dec;3(4):260-9. PMID: 8969008

MMR additional miscellany

73. Geier DA, Geier MR. A comparative evaluation of the effects of

MMR immunization and mercury doses from thimerosal-containing

childhood vaccines on the population prevalence of autism. Med Sci

Monit. 2004 Mar;10(3):PI33-9. Epub 2004 Mar 01. PMID: 14976450

" These studies have shown that there is biological plausibility and

epidemiological evidence showing a direct relationship between

increasing doses of mercury from thimerosal-containing vaccines and

neurodevelopmental disorders, and measles-containing vaccines and

serious neurological disorders. It is recommended that thimerosal be

removed from all vaccines, and additional research be undertaken to

produce a MMR vaccine with an improved safety profile. "

74. Vijendra K. Singh, Ph.D. Autism, Vaccines, and Immune Reactions.

IOM presentation, Feb 9, 2004.

Audio only: http://www.iom.edu/view.asp?id=19132

75. Singh VK, Jensen RL. Elevated levels of measles antibodies in

children with autism. Pediatr Neurol. 2003 Apr;28(4):292-4. PMID:

12849883

" Virus-induced autoimmunity may play a causal role in autism. To

examine the etiologic link of viruses in this brain disorder, we

conducted a serologic study of measles virus, mumps virus, and

rubella virus. Viral antibodies were measured by enzyme-linked

immunosorbent assay in the serum of autistic children, normal

children, and siblings of autistic children. The level of measles

antibody, but not mumps or rubella antibodies, was significantly

higher in autistic children as compared with normal children (P =

0.003) or siblings of autistic children (P <or= 0.0001).

Furthermore, immunoblotting of measles vaccine virus revealed that

the antibody was directed against a protein of approximately 74 kd

molecular weight. The antibody to this antigen was found in 83% of

autistic children but not in normal children or siblings of autistic

children. Thus autistic children have a hyperimmune response to

measles virus, which in the absence of a wild type of measles

infection might be a sign of an abnormal immune reaction to the

vaccine strain or virus reactivation. "

76. Singh VK et al. Abnormal measles-mumps-rubella antibodies and

CNS autoimmunity in children with autism. J Biomed Sci. 2002 Jul-

Aug;9(4):359-64. PMID 12145534

" Autoimmunity to the central nervous system (CNS), especially to

myelin basic protein (MBP), may play a causal role in autism, a

neurodevelopmental disorder. Because many autistic children harbor

elevated levels of measles antibodies, we conducted a serological

study of measles-mumps-rubella (MMR) and MBP autoantibodies. Using

serum samples of 125 autistic children and 92 control children,

antibodies were assayed by ELISA or immunoblotting methods. ELISA

analysis showed a significant increase in the level of MMR

antibodies in autistic children. Immunoblotting analysis revealed

the presence of an unusual MMR antibody in 75 of 125 (60%) autistic

sera but not in control sera. This antibody specifically detected a

protein of 73-75 kD of MMR. This protein band, as analyzed with

monoclonal antibodies, was immunopositive for measles hemagglutinin

(HA) protein but not for measles nucleoprotein and rubella or mumps

viral proteins. Thus the MMR antibody in autistic sera detected

measles HA protein, which is unique to the measles subunit of the

vaccine. Furthermore, over 90% of MMR antibody-positive autistic

sera were also positive for MBP autoantibodies, suggesting a strong

association between MMR and CNS autoimmunity in autism. Stemming

from this evidence, we suggest that an inappropriate antibody

response to MMR, specifically the measles component thereof, might

be related to pathogenesis of autism. "

77. Singh VK et al. Serological association of measles virus and

human herpesvirus-6 with brain autoantibodies in autism. Clin

Immunol Immunopathol 1998 89(1):105-8. PMID: 9756729

" Considering an autoimmunity and autism connection, brain

autoantibodies to myelin basic protein (anti-MBP) and neuron-axon

filament protein (anti-NAFP) have been found in autistic children.

In this current study, we examined associations between virus

serology and autoantibody by simultaneous analysis of measles virus

antibody (measles-IgG), human herpesvirus-6 antibody (HHV-6-IgG),

anti-MBP, and anti-NAFP. We found that measles-IgG and HHV-6-IgG

titers were moderately higher in autistic children but they did not

significantly differ from normal controls. Moreover, we found that a

vast majority of virus serology-positive autistic sera was also

positive for brain autoantibody: (i) 90% of measles-IgG-positive

autistic sera was also positive for anti-MBP; (ii) 73% of measles-

IgG-positive autistic sera was also positive for anti-NAFP; (iii)

84% of HHV-6-IgG-positive autistic sera was also positive for anti-

MBP; and (iv) 72% of HHV-6-IgG-positive autistic sera was also

positive for anti-NAFP. This study is the first to report an

association between virus serology and brain autoantibody in autism;

it supports the hypothesis that a virus-induced autoimmune response

may play a causal role in autism. "

vMV, MV & immunity

78. Hussey GD et al. The effect of Edmonston-Zagreb and Schwarz

measles vaccines on immune response in infants. J Infect Dis. 1996

Jun; 173(6): 1320-6 PMID: 8648203

The effects of measles immunization on immune responses in infants

and the roles of vaccine strain and age of immunization are not

known. Eighty-eight children were immunized at 6 or 9 months of age

with the Edmonston-Zagreb (EZ) or Schwarz (SW6, SW9) strain of

measles vaccine… Therefore, measles immunization resulted in

suppression of lymphoproliferation, which was most evident in

infants with the highest antibody responses and most immune

activation. "

79. Auwaerter PG et al. Changes within T cell receptor V beta

subsets in infants following measles vaccination. Hopkins

University School of Medicine, Baltimore, MD 21287, USA. Clin

Immunol Immunopathol 1996 79(2): 163-70. PMID: 8620622

" Measles produces immune suppression which contributes to an

increased susceptibility to other infections. These data suggest

that [vaccinal and wild-type] measles virus may affect immune

responses in part by altering the T cell receptor repertoire. "

80. Schneider-Schaulies S, ter Meulen V. Triggering of and

interference with immune activation: interactions of measles virus

with monocytes and dendritic cells. Viral Immunol. 2002;15(3):417-

28. PMID: 12479392

81. Measles virus suppresses cell-mediated immunity by interfering

with the survival and functions of dendritic and T cells. J Exp Med

1997;186:813-23

82. Sonoda S, Nakayama T. Detection of measles virus genome in

lymphocytes from asymptomatic healthy children. J Med Virol 2001 65

(2):381-7 PMID: 11536248

" In 83 individuals immunized with measles vaccine, the vaccine

strain genome was detected in 10 (71.4%) of 14 recipients whose PBMC

were obtained within 2 months of vaccination. "

83. Valsamakis A et al. Strains of measles vaccine differ in their

ability to replicate in an damage human thymus. J Infect Dis. 2001

Feb 1; 183(3): 498-502. s Hopkins University, Baltimore,

land, USA. PMID: 11133383

[Question: How would the thymic-damage findings be exacerbated if

tested tissues were selected to represent humans with excessively

increased susceptibility, eg, an infant with persisting colic and/or

persisting otitis?]

MV & Vitamin A

84. Yalcin SS et al. The effect of live measles vaccines on serum

vitamin A levels in healthy children. Acta Paediatr Jpn. 1998 Aug;

40(4): 345-9. PMID: 9745778

" Serum retinol levels have been shown to be depressed during measles

infection. This study aims to demonstrate whether there is any

decrease in serum vitamin A level following immunization with live

viral vaccine and its relation with vaccine seroconversion in

children with measles. Since many children receive measles vaccine

alone or in combination with measles-mumps-rubella vaccine, we

studied serum vitamin A levels and antibody levels in healthy, well-

nourished children before and after immunization with monovalent and

combined live attenuated measles vaccine… CONCLUSION: Serum vitamin

A levels are reduced following vaccination with monovalent and

combined live attenuated measles vaccines. "

85. Vitamin A administered with measles vaccine to nine-month-old

infants does not reduce vaccine immunogenicity. J Nutr. 1999 Aug;

129(8): 1569-73. PMID 10419992

http://www.nutrition.org/cgi/reprint/129/8/1569.pdf

" Among malnourished infants, the geometric mean titer was

significantly greater in the vitamin A group compared to the placebo

group (ratio of geometric means, 1.57; 95% confidence interval, 1.

18-2.0), but seroconversion rates did not differ. "

[Comment: note the theoretical implication that malourished children

may have lower cell-mediated immunity and thus generate increased

antibody immunity. This is consistent with immunity lab-data in many

autistic children.]

86. Yalcin SS, Yurdakok K. Sex-specific differences in serum vitamin

A values after measles immunization. Pediatr Infect Dis J. 1999

Aug; 18(8): 747-8. PMID 10462357

87. Semba RD. Vitamin A and immunity to viral, bacterial and

protozoan infections. Proc Nutr Soc 1999 58(3): 719-27. PMID

10604208

" …vitamin A and related retinoids play a major role in immunity,

including expression of mucins and keratins, lymphopoiesis,

apoptosis, cytokine expression, production of antibody, and the

function of neutrophils, natural killer cells, monocytes or

macrophages, T lymphocytes and B lymphocytes. Recent clinical trials

suggest that vitamin A supplementation reduces morbidity and

mortality in different infectious diseases, such as measles,

diarrhoeal disease, measles-related pneumonia, human

immunodeficiency virus infection and malaria. Immune responses vary

considerably during different infections, and the available data

suggest that the modulation of immune function by vitamin A may also

vary widely, depending on the type of infection and immune responses

involved. "

88. Molina EL, Patel JA. A to Z: vitamin A and zinc, the miracle

duo. Indian J Pediatr. 1996 63(4): 427-31. PMID 10832460

" Dietary micronutrients such as vitamins and trace minerals are

known modulators of host immune responses against common pathogens.

In this respect, vitamin A and zinc have recently received increased

attention. Several in vivo and in vitro studies suggest that vitamin

A may be a critical player in the mucosal immune responses in the

respiratory and gastrointestinal tracts, particularly in

undernourished children. The effect may be mediated primarily by

stabilization of the membrane of mucosal epithelial cells, as well

as enhanced leukocyte functions. The beneficial effect of vitamin A

therapy in reducing measles-associated morbidity and mortality

suggests its crucial role in defenses against viral pathogens. Zinc

is also known affect leukocyte functions such as phagocytosis and T-

lymphocyte-mediated immune responses… Dietary supplementation or

therapeutic treatment with vitamin A and zinc may be a cheap yet

effective means of preventing or treating infections in highly

susceptible populations. Additional studies, however, are required

to better define the types of pathogens and the specific human

populations that may benefit from such therapy. "

88b. Chandra RK, Wadhwa M. Nutritional modulation of intestinal

mucosal immunity. Immunol Invest. 1989 Jan-May;18(1-4):119-26.

PMID: 2659508

" Protein-energy malnutrition results in an increased risk of

gastrointestinal infection. This can be attributed in part to

impaired immune responses. Cell-mediated immunity is decreased as

judged by reduced number and function of thymus-dependent

lymphocytes, impaired delayed cutaneous hypersensitivity reactions,

and decreased production of lymphokines. Concentration of secretory

IgA is reduced and there are fewer intraepithelial lymphocytes.

Antibody responses following viral vaccine administration are

reduced and there is decrease in natural killer cell activity. In

addition, the number of bacteria binding to epithelial cells is

increased. These changes are observed also in certain selected

nutrient deficiencies, such as that of vitamin A. It is suggested

that impaired systemic and mucosal immunity contributes to the

increased frequency and severity of intestinal infections seen in

undernourished individuals. "

88c. Lie C et al. Impact of large-dose vitamin A supplementation on

childhood diarrhoea, respiratory disease and growth. Eur J Clin

Nutr. 1993 Feb;47(2):88-96. PMID: 8436094

" One hundred and seventy-two 0.5-3.0-year-old children in a

mountainous area of northern Hebei Province of China were randomly

assigned to a vitamin A supplementation group (n = 98) or a control

group (n = 74) for a 1 year double-blind study. Capsules containing

200,000 IU vitamin A and 40 IU vitamin E were given to the children

in the experimental group 3 and 9 months after baseline examination.

During the 12 month study period, there was a significant reduction

in the incidence of diarrhoea (P < 0.01) and respiratory disease (P

< 0.01) in the children of the experimental group compared to the

control. Risk of diarrhoea and respiratory disease were respectively

2.5 and 3.4 times higher in the control children. Serum retinol and

IgA levels of the treatment group were significantly higher than

that of control group (P < 0.01) 7 weeks after first

supplementation. There was no significant difference in saliva IgA

level between groups. No significant differences in growth were

observed. It was concluded that supplementation with large doses of

vitamin A decreased the incidence and severity of diarrhoea and

respiratory disease in these children, possibly through enhanced

activity of the immune system, but had no effect on growth over 1

year. "

88d. Sarkar J et al. Vitamin A is required for regulation of

polymeric immunoglobulin receptor (pIgR) expression by interleukin-4

and interferon-gamma in a human intestinal epithelial cell line. J

Nutr. 1998 Jul;128(7):1063-9. PMID: 9649586

" The secretory immunoglobulin A (IgA) antibody response to

infections of mucosal surfaces requires transport of IgA from the

basal to apical surface of mucosal epithelial cells by a specific

transport protein, the polymeric immunoglobulin receptor (pIgR). We

have tested the hypothesis that the vitamin A metabolite all-trans

retinoic acid (RA) is required for the regulation of pIgR expression

by the cytokines interleukin-4 (IL-4) and interferon-gamma (IFN-

gamma) in HT-29 cells… These data indicate that RA strongly

interacts with IL-4 and IFN-gamma to regulate pIgR expression in HT-

29 cells, suggesting that vitamin A may be required for proper in

vivo regulation of IgA transport in response to mucosal infections. "

88e. Nikawa T et al. Vitamin A prevents the decline in

immunoglobulin A and Th2 cytokine levels in small intestinal mucosa

of protein-malnourished mice. J Nutr 1999 129(5):934-41. PMID:

10222382

" These results suggest that large oral supplements of vitamin A may

preserve mucosal IgA level during protein malnutrition, possibly by

stimulating Th2 cytokine production and thereby, inducing resistance

against infection. "

88f. Aukrust P et al. pal.aukrust@... Decreased vitamin

A levels in common variable immunodeficiency: vitamin A

supplementation in vivo enhances immunoglobulin production and

downregulates inflammatory responses. Eur J Clin Invest. 2000 30

(3):252-9. PMID: 10692003

" BACKGROUND: Vitamin A has a broad range of immunological effects,

and vitamin A deficiency is associated with recurrent infections.

Common variable immunodeficiency (CVI) is a group of B-cell

deficiency syndromes with impaired antibody production and recurrent

bacterial infections as the major manifestations, but the

immunological dysfunctions may also include T cells and macrophages.

In the present study we examined the possible role of vitamin A

deficiency in CVI… CONCLUSION: A considerable subgroup of CVI

patients appears to be characterized by low vitamin A levels. Our

findings support a possible role for vitamin A supplementation in

CVI, perhaps resulting in enhanced immunoglobulin synthesis and

downregulated inflammatory responses.

88g. Bjersing JL et al. jan.bjersing@... Loss of ileal

IgA+ plasma cells and of CD4+ lymphocytes in ileal Peyer's patches

of vitamin A deficient rats. Clin Exp Immunol. 2002 Dec;130(3):404-

8. PMID: 12452829

" Child mortality in diarrhoeal disease is increased significantly by

vitamin A deficiency in poor countries. The pathological mechanisms

are not known in detail. However, in this paper we report that

vitamin A-deficient Wistar rats had much reduced IgA+ plasma cells

in the ileal lamina propria (eightfold reduction from 470 cells/mm

(2), P = 0.009), as well as a prominent reduction of CD4+ cells in

the parafollicular regions of ileal Peyer's patches (reduction from

7200 to 105 cells/mm(2), P = 0.009). IL-2Ralpha-chain (CD25)

positive lymphocytes in the ileal Peyer's patches were also reduced

significantly in vitamin A deficiency (from 1400 to 300 cells/mm(2),

P = 0.009). The density of CD8 cells tended to be increased relative

to the control animals (from 5100 to 6000 cells/mm(2), not

statistically significant). In conclusion, the marked decrease of

lamina propria IgA+ plasma cells may be one cause of the high

diarrhoeal mortality in vitamin A deficiency. This, in turn, appears

to be related to reduced numbers of activated or regulatory CD4+ T

cells in Peyer's patches.

88h. Kim JY, Chung BH. Effects of combination dietary conjugated

linoleic acid with vitamin A (retinol) and selenium on the response

of the immunoglobulin production in mice. J Vet Sci. 2003 Apr;4

(1):103-8. PMID: 12819373

" The dietary effect of conjugated linoleic acid (CLA) on the

response of the immunoglobulin (serum and tissue) production in

Balb/C mice was examined at three doses: 0 %(control), 0.5% and

1.5%. The combination effects of CLA with vitamin ADE or selenium

also were investigated. CLA at 0.5% increased serum immunoglobulin

A, G, mesenteric lymph node (MHN) and gut luminal IgA (secretory

IgA) levels. However, 1.5% CLA decreased SIgG slightly. CLA both

alone and combined with vitamin ADE and selenium did not affect

serum IgE. The levels of immunoglobulin concentration in the 0.5%

CLA group were higher than those in the 1.5% CLA group. The level of

serum IgG in 1.5% CLA combined with selenium was maintained at the

same level as that of control. It is considered that overdoses of

CLA (1.5%) even depressed the production of immunoglobulin but

selenium and/or vitamin inhibited this activity to a certain

extent.In this study, dietary CLA increased immunoglobulin

production in a dose-dependent manner. Vitamin ADE and Selenium

combined with CLA also increased the immunoglobulin production

response except serum IgE.

89. D'Souza RM, D'Souza R. Vitamin A for preventing secondary

infections in children with measles—a systematic review. J Trop

Pediatr. 2002 48(2):72-7. PMID 12022432

90. D'Souza RM, D'Souza R. Vitamin A for treating measles in

children. Cochrane Database Syst Rev. 2002;(1):CD001479. PMID

11869601

" REVIEWER'S CONCLUSIONS: Although we did not find evidence that a

single dose of 200,000 IU of vitamin A per day was associated with

reduced mortality among children with measles, there was evidence

that the same dose given for two days was associated with a reduced

risk of overall mortality and pneumonia specific mortality. The

effect was greater in children under the age of two years. "

91. Madhulika et al. Vitamin A supplementation in post-measles

complications. J Trop Pediatr. 1994 Oct;40(5):305-7. PMID 7807628.

The case fatality rate was 16 per cent in those who received VIT.A,

while the same was 32 per cent in those who did not receive Vit.A (P

< 0.02). "

92. Hussey GD, Klein M. Routine high-dose vitamin A therapy for

children hospitalized with measles. J Trop Pediatr. 1993 39(6):342-

5. PMID 8133555

Measles is without specific therapy and remains important globally

as a cause of childhood death. In controlled studies, high-dose

vitamin A therapy (Hi-VAT)—with 400,000 IU vitamin A--has been

demonstrated to markedly reduce measles-associated morbidity and

mortality. "

93. JC et al. Measles severity and serum retinol (vitamin A)

concentration among children in the United States. Pediatrics. 1993

Jun;91(6):1176-81. PMID 8502524

94. Bluhm DP, Summers RS. Plasma vitamin A levels in measles and

malnourished pediatric patients and their implications in

therapeutics. J Trop Pediatr 1993 39(3):179-82. PMID 8326539

This study has shown that there is a high incidence of baseline

hyporetinaemia in these patients. The mean retinol plasma levels

return to within normal limits after 8 days of either routine

treatment or vitamin A supplementation. "

95. Ogaro FO et al. Effect of vitamin A on diarrhoeal and

respiratory complications of measles. Trop Geogr Med. 1993;45

(6):283-6. PMID 8116059

" These findings, along with those from three other trials in Africa,

suggest that high dose vitamin A reduces the severity of

complications during measles. "

96. Coutsoudis A et al. Vitamin A supplementation enhances specific

IgG antibody levels and total lymphocyte numbers while improving

morbidity in measles. Pediatr Infect Dis J. 1992 11(3):203-9. PMID

1565535

These findings reinforce results from animal studies that show that

the pathways of vitamin A activity in decreasing morbidity and

mortality are partly founded on selective immunopotentiation. "

97. Frieden TR et al. Vitamin A levels and severity of measles. New

York City. Am J Dis Child. 1992 Feb;146(2):182-6. PMID 1285727

Recent studies show that vitamin A levels decrease during measles

and that vitamin A therapy can improve measles outcome in children

in the developing world. Vitamin A levels of children with measles

have not been studied in developed countries. We therefore measured

vitamin A levels in 89 children with measles younger than 2 years

and in a reference group in New York City, NY. Vitamin A levels in

children with measles ranged from 0.42 to 3.0 mumol/L; 20 (22%) were

low. Children with low levels were more likely to have fever at a

temperature of 40 degrees C or higher (68% vs 44%), to have fever

for 7 days or more (54% vs 23%), and to be hospitalized (55% vs

30%). Children with low vitamin A levels had lower measles-specific

antibody levels. No child in the reference group had a low vitamin A

level. Our data show that many children younger than 2 years in New

York City have low vitamin A levels when ill with measles, and that

such children seem to have lower measles-specific antibody levels

and increased morbidity. Clinicians may wish to consider vitamin A

therapy for children younger than 2 years with severe measles… "

Autism, malnutrition, flora

98: Owens, DAN! Think-tank presentation. Philadelphia 2003.

99. Finegold SM et al. Gastrointestinal microflora studies in late-

onset autism. Clin Infect Dis 2002 35(Suppl 1):S6-S16 PMID 12173102

" Some cases of late-onset (regressive) autism may involve abnormal

flora because oral vancomycin, which is poorly absorbed, may lead to

significant improvement in these children. Fecal flora of children

with regressive autism was compared with that of control children,

and clostridial counts were higher. The number of clostridial

species found in the stools of children with autism was greater than

in the stools of control children. Children with autism had 9

species of Clostridium not found in controls, whereas controls

yielded only 3 species not found in children with autism. In all,

there were 25 different clostridial species found. In gastric and

duodenal specimens, the most striking finding was total absence of

non-spore-forming anaerobes and microaerophilic bacteria from

control children and significant numbers of such bacteria from

children with autism. These studies demonstrate significant

alterations in the upper and lower intestinal flora of children with

late-onset autism and may provide insights into the nature of this

disorder. "

100. Bendel CM. Colonization and epithelial adhesion in the

pathogenesis of neonatal candidiasis. Semin Perinatol. 2003 Oct;27

(5):357-64. PMID 14626499

" C albicans is the most commonly isolated species in colonized or

infected infants. Over the past decade the incidence of both

colonization and infection with other Candida species, particularly

C parapsilosis, has risen dramatically… Microbial factors also

augment colonization, including the ability of Candida to adhere to

human epithelium. "

101. WA. Role of nutrients and bacterial colonization in the

development of intestinal host defense. J Pediatr Gastroenterol

Nutr. 2000;30 Suppl 2:S2-7. PMID 10749395

102. Dai D, WA. Protective nutrients and bacterial

colonization in the immature human gut. Adv Pediatr. 1999;46:353-

82. PMID 10645469

" The normal human microflora is a complex ecosystem that is in part

dependent on enteric nutrients for establishing colonization. The

gut microbiota are important to the host with regard to metabolic

functions and resistance to bacterial infections. At birth,

bacterial colonization of a previously germ-free human gut begins.

Diet and environmental conditions can influence this ecosystem. A

breast-fed, full-term infant has a preferred intestine microbiota in

which bifidobacteria predominate over potentially harmful bacteria,

whereas in formula-fed infants, coliforms, enterococci, and

bacteroides predominate. The pattern of bacterial colonization in

the premature neonatal gut is different from that in the healthy,

full-term infant gut… Probiotics and prebiotics modulate the

composition of the human intestinal microflora to the benefit of the

host. These beneficial effects may result in the suppression of

harmful microorganisms, the stimulation of bifidobacterial growth,

or both. In the future, control and manipulation of the bacterial

colonization… may be a new approach to the prevention and treatment

of intestinal infectious diseases of various etiologies. "

103. Orrhage K, Nord CE. Factors controlling the bacterial

colonization of the intestine in breastfed infants. Acta Paediatr

Suppl. 1999 Aug;88(430):47-57. PMID 10569223

" This article summarizes the published data on the intestinal

microflora in breastfed infants published during the last 15 y.

Enterobacteria and enterococci are found in high numbers in most

infants during the first week of life. Bifidobacteria and

Bacteroides spp. are found in increasing numbers at the following

weeks. The intestinal microflora in breastfed infants can also be

followed by different biochemical parameters. Acetic acid is found

in higher concentrations in breastfed than in formula-fed infants.

Degradation of mucin starts later in breastfed than in formula-fed

infants. The conversion of cholesterol to coprostanol is also

delayed by breastfeeding. Geographical differences in the

composition of the intestinal microflora in infants have been

reported, i.e. enterobacteria, enterococci, bifidobacteria,

lactobacilli and bacteroides show different occurrences in developed

and developing countries. There are minor differences in the

infant's intestinal microflora due to breastfeeding or/and formula

feeding. "

104. Belley A et al. Intestinal mucins in colonization and host

defense against pathogens. Am J Trop Med Hyg. 1999 Apr;60(4

Suppl):10-5 PMID 10344672

" Intestinal mucins are key components of the first line of host

defense against intestinal pathogens. These large glycoconjugates

secreted by specialized exocrine goblet cells form viscous gels that

trap microorganisms and irritants and limit their diffusion to the

intestinal epithelium. Moreover, they allow for colonization by

indigenous bacterial flora that prevents attachment of pathogenic

microbes. The interaction between microbes and mucins involves mucin

carbohydrate side chains and microbial adhesin molecules. Certain

microorganisms and disease states may alter mucin biochemistry or

expression… "

105. Jarvis WR. The epidemiology of colonization. Infect Control

Hosp Epidemiol. 1996 Jan;17(1):47-52. PMID 8789688

" Colonization is the presence of a microorganism in or on a host,

with growth and multiplication but without any overt clinical

expression or detected immune response in the host at the time it is

isolated. Normal colonization in humans begins during the birth

process and through subsequent contacts with the inanimate or

animate environments until a delicately balanced " normal " flora is

established; subsequently, the precise components of this flora

evolve. This normal flora, such as coagulase-negative Staphylococcus

or Staphylococcus aureus on the skin or Candida albicans in the

gastrointestinal tract, vagina, or perineal area, can result in

infection when normal body defenses are impaired through underlying

disease, immunomodulating therapy, or the use of invasive devices,

or when the delicate balance of the normal flora is altered through

antimicrobial therapy… "

106. Fitzgerald JF. Colonization of the gastrointestinal tract. Mead

Symp Perinat Dev Med. 1977;(11):35-8. PMID 347190

" The alimentary tract is sterile at birth but colonic colonization

is relatively complete by the end of the first week of life. The

upper alimentary tract is colonized by microorganisms normally

inhabiting the oral cavity. The colon on the other hand appears to

be colonized by microorganisms originating in the maternallower

alimentary tract. The colonic flora of infants is affected by diet

(breast or formula feedings). The presence of a " fecal-type " flora

in the proximal small bowel should be considered abnormal… "

Gastrointestinal miscellany

107. Edelson SB, Cantor DS. Autism: xenobiotic influences. Toxicol

Ind Health. 1998 Jul-Aug;14(4):553-63. PMID 9664646

" The advances in medical technology during the last four decades has

provided evidence for an underlying neurological basis for autism.

The etiology for the variations of neurofunctional anomalies found

in the autistic spectrum behaviors appears inconclusive as of this

date but growing evidence supports the proposal that chronic

exposure to toxic agents, i.e., xenobiotic agents, to a developing

central nervous system may be the best model for defining the

physiological and behavioral data found in these populations. A

total of 20 subjects (15 males and 5 females) who received a formal

diagnosis of autism by a developmental pediatrician, pediatric

neurologist, or licensed psychologist were included. The mean age

for the sample was 6.35 yrs offnge = 3-12 years)… It is most

noteworthy that of the 20 cases examined for this study, 100% of the

cases showed liver detoxication profiles outside of normal. An

examination of 18 autistic children in blood analyses that were

available showed that 16 of these children showed evidence of levels

of toxic chemicals exceeding adult maximum tolerance. [Chelation

challenge is more accurately instructive.] In the two cases where

toxic chemical levels were not found, there was abnormal D-glucaric

acid findings suggesting abnormal xenobiotic influences on liver

detoxication processes. A proposed mechanism for the interaction of

xenobiotic toxins with immune system dysfunction and continuous

and/or progressive endogenous toxicity is presented as it relates to

the development of behaviors found in the autistic spectrum.

108. Thony B et al. Tetrahydrobiopterin biosynthesis, regeneration

and functions. Biochem J. 2000 347 Pt 1:1-16. PMID 10727395

109. Cohen BI. The significance of ammonia/gamma-aminobutyric acid

(GABA) ratio for normality and liver disorders. Med Hypotheses.

2002 Dec;59(6):757-8. PMID 12445521

110. Kidd PM Autism, an extreme challenge to integrative medicine.

Part: 1: The knowledge base. Altern Med Rev. 2002 Aug;7(4):292-

316. PMID: 12197782

" Autism, archetype of the autistic spectrum disorders (ASD), is a

neurodevelopmental disorder characterized by socially aloof behavior

and impairment of language and social interaction. Its prevalence

has surged in recent years. Advanced functional brain imaging has

confirmed pervasive neurologic involvement. Parent involvement in

autism management has accelerated understanding and treatment. Often

accompanied by epilepsy, cognitive deficits, or other neurologic

impairment, autism manifests in the first three years of life and

persists into adulthood. Its etiopathology is poorly defined but

likely multifactorial with heritability playing a major role.

Prenatal toxic exposures (teratogens) are consistent with autism

spectrum symptomatology. Frequent vaccinations with live virus and

toxic mercurial content (thimerosal) are a plausible etiologic

factor. Autistic children frequently have abnormalities of

sulfoxidation and sulfation that compromise liver detoxification,

which may contribute to the high body burden of xenobiotics

frequently found. Frequent copper-zinc imbalance implies

metallothionein impairment that could compound the negative impact

of sulfur metabolism impairments on detoxification and on intestinal

lining integrity. Intestinal hyperpermeability manifests in autistic

children as dysbiosis, food intolerances, and exorphin (opioid)

intoxication, most frequently from casein and gluten. Immune system

abnormalities encompass derangement of antibody production, skewing

of T cell subsets, aberrant cytokine profiles, and other impairments

consistent with chronic inflammation and autoimmunity. Coagulation

abnormalities have been reported. "

111. Kidd PM. Autism, an extreme challenge to integrative medicine.

Part 2: medical management. Altern Med Rev. 2002 Dec;7(6):472-99.

PMID 12495373

" Autism and allied autistic spectrum disorders (ASD) present myriad

behavioral, clinical, and biochemical abnormalities. Parental

participation, advanced testing protocols, and eclectic treatment

strategies have driven progress toward cure. Behavioral modification

and structured education are beneficial but insufficient. Dietary

restrictions, including removal of milk and other casein dairy

products, wheat and other gluten sources, sugar, chocolate,

preservatives, and food coloring are beneficial and prerequisite to

benefit from other interventions. Individualized IgG or IgE testing

can identify other troublesome foods but not non-immune mediated

food sensitivities. Gastrointestinal improvement rests on

controlling Candida, [parasites and pathogenic bacteria], and using

probiotic bacteria and nutrients to correct dysbiosis and decrease

gut permeability. Detoxification of mercury and other heavy metals

by DMSA/DMPS chelation can have marked benefit. Documented

sulfoxidation-sulfation inadequacies call for sulfur-sulfhydryl

repletion and other liver p450 support. Many nutrient supplements

are beneficial and well tolerated, including dimethylglycine (DMG)

and a combination of pyridoxine (vitamin B6) and magnesium, both of

which benefit roughly half of ASD cases. Vitamins A, B3, C, and

folic acid; the minerals calcium and zinc; cod liver oil; and

digestive enzymes, all offer benefit… Current pharmaceuticals fail

to benefit the primary symptoms and can have marked adverse effects.

Individualized, in-depth clinical and laboratory assessments and

integrative parent-physician-scientist cooperation are the keys to

successful ASD management. "

112. Kidd PM. An approach to the nutritional management of autism.

Altern Ther Health Med. 2003 Sep-Oct;9(5):22-31 PMID 14526708

Glutathione

113. Wang XF, Cynader MS. Astrocytes provide cysteine to neurons by

releasing glutathione. J Neurochem. 2000 74(4):1434-42. PMID

10737599

" Cysteine is the rate-limiting precursor of glutathione synthesis.

Evidence suggests that astrocytes can provide cysteine and/or

glutathione to neurons. However, it is still unclear how cysteine is

released and what the mechanisms of cysteine maintenance by

astrocytes entail. In this report, we analyzed cysteine,

glutathione, and related compounds in astrocyte conditioned medium

using HPLC methods. In addition to cysteine and glutathione,

cysteine-glutathione disulfide was found in the conditioned medium.

In cystine-free conditioned medium, however, only glutathione was

detected. These results suggest that glutathione is released by

astrocytes directly and that cysteine is generated from the

extracellular thiol/disulfide exchange reaction of cystine and

glutathione: glutathione + cystine<-->cysteine + cysteine-

glutathione disulfide. Conditioned medium from neuron-enriched

cultures was also assayed in the same way as astrocyte conditioned

medium, and no cysteine or glutathione was detected. This shows that

neurons cannot themselves provide thiols but instead rely on

astrocytes. We analyzed cysteine and related compounds in rat CSF

and in plasma of the carotid artery and internal jugular vein. Our

results indicate that cystine is transported from blood to the CNS

and that the thiol/disulfide exchange reaction occurs in the brain

in vivo. Cysteine and glutathione are unstable and oxidized to their

disulfide forms under aerobic conditions. Therefore, constant

release of glutathione by astrocytes is essential to maintain stable

levels of thiols in the CNS. "

114. Fonnum F, Lock EA. The contributions of excitotoxicity,

glutathione depletion and DNA repair in chemically induced injury to

neurones: exemplified with toxic effects on cerebellar granule

cells. J Neurochem. 2004 Feb;88(3):513-31. PMID: 14720201

" Six chemicals, 2-halopropionic acids, thiophene, methylhalides,

methylmercury, methylazoxymethanol (MAM) and trichlorfon (Fig. 1),

that cause selective necrosis to the cerebellum, in particular to

cerebellar granule cells, have been reviewed… All six compounds

decrease cerebral glutathione (GSH), due to conjugation with the

xenobiotic, thereby reducing cellular antioxidant status and making

the cells more vulnerable to reactive oxygen species. 2-

Halopropionic acids and methylmercury appear to also act via an

excitotoxic mechanism leading to elevated intracellular Ca2+,

increased reactive oxygen species and ultimately impaired

mitochondrial function… We propose that a combination of reduced

antioxidant status plus excitotoxicity or DNA damage is required to

cause cerebellar neuronal cell death with these chemicals. The small

size of cerebellar granule cells, the unique subunit composition of

their N-methyl-d-aspartate (NMDA) receptors, their low DNA repair

ability, low levels of calcium-binding proteins and vulnerability

during postnatal brain development and distribution of glutathione

and its conjugating and metabolizing enzymes are all important

factors in determining the sensitivity of cerebellar granule cells

to toxic compounds. "

115. Ehrhart J, Zeevalk GD. ative interaction between

ascorbate and glutathione during mitochondrial impairment in

mesencephalic cultures. J Neurochem 2003 86(6):1487-97. PMID:

12950457

" These findings indicate that ascorbate contributes to the

maintenance of GSSG/GSH status during oxidative stress through

scavenging of radical species, attenuation of GSH efflux and

redistribution of GSSG to the formation of mixed disulfides. It is

speculated that these events are linked by glutaredoxin, an enzyme

shown to contain both dehydroascorbate reductase as well as

glutathione thioltransferase activities. "

116. Dringen R, Hirrlinger J. Glutathione pathways in the brain.

Biol Chem. 2003 384(4):505-16. PMID: 12751781

" The antioxidant glutathione (GSH) is essential for the cellular

detoxification of reactive oxygen species in brain cells. A

compromised GSH system in the brain has been connected with the

oxidative stress occuring in neurological diseases. Recent data

demonstrate that besides intracellular functions GSH has also

important extracellular functions in brain. In this respect

astrocytes appear to play a key role in the GSH metabolism of the

brain, since astroglial GSH export is essential for providing GSH

precursors to neurons. Of the different brain cell types studied in

vitro only astrocytes release substantial amounts of GSH. In

addition, during oxidative stress astrocytes efficiently export

glutathione disulfide (GSSG)…. This review focuses on recent

results on the export of GSH and GSSG from brain cells as well as on

the functions of extracellular GSH in the brain. In addition,

implications of disturbed GSH pathways in brain for

neurodegenerative diseases will be discussed. "

117. Pastore A et al. Analysis of glutathione: implication in redox

and detoxification. Clin Chim Acta. 2003 Jul 1;333(1):19-39. PMID:

12809732

" BACKGROUND: Glutathione is a ubiquitous thiol-containing

tripeptide, which plays a central role in cell biology. It is

implicated in the cellular defence against xenobiotics and naturally

occurring deleterious compounds, such as free radicals and

hydroperoxides… Glutathione is a critical factor in protecting

organisms against toxicity and disease. This review may turn useful

for analysing the glutathione homeostasis, whose impairment

represents an indicator of tissue oxidative status in human

subjects. "

118. Sheehan D et al. Structure, function and evolution of

glutathione transferases: implications for classification of non-

mammalian members of an ancient enzyme superfamily. Biochem J. 2001

Nov 15;360(Pt 1):1-16. PMID: 11695986

" The glutathione transferases (GSTs; also known as glutathione S-

transferases) are major phase II detoxification enzymes found mainly

in the cytosol. In addition to their role in catalysing the

conjugation of electrophilic substrates to glutathione (GSH), these

enzymes also carry out a range of other functions. "

119. JD, Strange RC. Glutathione S-transferase polymorphisms

and their biological consequences. Pharmacology. 2000 Sep;61(3):154-

66. PMID: 10971201

" Two supergene families encode proteins with glutathione S-

transferase (GST) activity: the family of soluble enzymes comprises

at least 16 genes; the separate family of microsomal enzymes

comprises at least 6 genes. These two GST families are believed to

exert a critical role in cellular protection against oxidative

stress and toxic foreign chemicals. They detoxify a variety of

electrophilic compounds, including oxidized lipid, DNA and catechol

products generated by reactive oxygen species-induced damage to

intracellular molecules. An increasing number of GST genes are being

recognized as polymorphic. Certain alleles, particularly those that

confer impaired catalytic activity (e.g. GSTM1(*)0, GSTT1(*)0), may

be associated with increased sensitivity to toxic compounds… "

120. Droge W, Breitkreutz R. Glutathione and immune function. Proc

Nutr Soc. 2000 Nov;59(4):595-600. PMID: 11115795

" The immune system works best if the lymphoid cells have a

delicately balanced intermediate level of glutathione. Even moderate

changes in the intracellular glutathione level have profound effects

on lymphocyte functions. Certain functions, such as the DNA

synthetic response, are exquisitely sensitive to reactive oxygen

intermediates and, therefore, are favoured by high levels of the

antioxidant glutathione. Certain signal pathways, in contrast, are

enhanced by oxidative conditions and favoured by low intracellular

glutathione levels. The available evidence suggests that the

lymphocytes from healthy human subjects have, on average, an optimal

glutathione level. There is no indication that immunological

functions such as resistance to infection or the response to

vaccination may be enhanced in healthy human subjects by

administration of glutathione or its precursor amino acid cysteine.

However, immunological functions in diseases that are associated

with a cysteine and glutathione deficiency may be significantly

enhanced and potentially restored by cysteine supplementation... "

121. Functions of glutathione and glutathione disulfide in

immunology and immunopathology. FASEB J. 1994 Nov;8(14):1131-8.

PMID: 7958618

" Even a moderate increase in the cellular cysteine supply elevates

the intracellular glutathione (GSH) and glutathione disulfide (GSSG)

levels and potentiates immunological functions of lymphocytes… "

122. Enhancement of tissue glutathione for antioxidant and immune

functions in malnutrition. Biochem Pharmacol. 1994 Jun 15;47

(12):2113-23. PMID: 8031307

123. Fernandez-Checa JC et al. Oxidative stress: role of

mitochondria and protection by glutathione. Biofactors. 1998;8(1-

2):7-11. PMID: 9699001

124. N-acetylcysteine. Altern Med Rev. 2000 Oct;5(5):467-71. PMID:

11056417 [No authors listed]

" N-acetylcysteine (NAC) is the acetylated precursor of both the

amino acid L-cysteine and reduced glutathione (GSH). Historically it

has been used as a mucolytic agent in chronic respiratory illnesses

as well as an antidote for hepatotoxicity due to acetaminophen

overdose. More recently, animal and human studies of NAC have shown

it to be a powerful antioxidant and a potential therapeutic agent in

the treatment of cancer, heart disease, HIV infection, heavy metal

toxicity, and other diseases characterized by free radical oxidant

damage. NAC has also been shown to be of some value in treating

Sjogren's syndrome, smoking cessation, influenza, hepatitis C, and

myoclonus epilepsy. "

125. Cai J et al. Inhibition of influenza infection by glutathione.

Free Radic Biol Med. 2003 Apr 1;34(7):928-36. PMID: 12654482

" Infection by RNA virus induces oxidative stress in host cells.

Accumulating evidence suggests that cellular redox status plays an

important role in regulating viral replication and infectivity. In

this study, experiments were performed to determine whether the

thiol antioxidant glutathione (GSH) blocked influenza viral

infection in cultures of Madin-Darby canine kidney cells or human

small airway epithelial cells. Protection against production of

active virus particles was observed at a low (0.05-0.1) multiplicity

of infection (MOI). GSH inhibited expression of viral matrix protein

and inhibited virally induced caspase activation and Fas

upregulation. In BALB/c mice, inclusion of GSH in the drinking water

decreased viral titer in both lung and trachea homogenates 4 d after

intranasal inoculation with a mouse-adapted influenza strain A/X-31.

Together, the data suggest that the thiol antioxidant GSH has an

anti-influenza activity in vitro and in vivo. Oxidative stress or

other conditions that deplete GSH in the epithelium of the oral,

nasal, and upper airway may, therefore, enhance susceptibility to

influenza infection.

Tylenol depletes GSH

126. Slattery JT et al. Dose-dependent pharmacokinetics of

acetaminophen: evidence of glutathione depletion in humans. Clin

Pharmacol Ther 1987 41(4):413-8 PMID 3829578

127. Lauterburg BH, JR. Therapeutic doses of acetaminophen

stimulate the turnover of cysteine and glutathione in man. J

Hepatol. 1987 Apr;4(2):206-11. PMID 3584929

" The data indicate that therapeutic doses of acetaminophen markedly

stimulate the rate of turnover of the pool of cysteine available for

the synthesis of GSH, most likely due to an increased rate of

synthesis of GSH which is required to detoxify the toxic metabolite

of acetaminophen. Patients who are not able to respond to a similar

demand on their stores of GSH by increasing the synthesis of GSH may

be at higher risk of developing hepatic injury from drugs that

require GSH for their detoxification. "

128. Spielberg SP. Acetaminophen toxicity in lymphocytes

heterozygous for glutathione synthetase deficiency. Can J Physiol

Pharmacol 1985 63(5):468-71 PMID 4041989

Heterozygous cells failed to use N-acetylcysteine as efficiently to

resynthesize glutathione, and the cells were not protected from

acetaminophen toxicity. Heterozygotes may be at increased risk of

toxicity from drugs whose metabolites are detoxified by glutathione

conjugation. "

129. Depletion of hepatic glutathione in rats impairs phagocytosis

in vivo. Arch Toxicol Suppl 1989;13:326-9 PMID 2774956

GSH & thimerosal

130. Homozygous gene deletions of the glutathione S-transferases M1

and T1 are associated with thimerosal sensitization. Int Arch Occup

Environ Health 2000 73(6):384-8 PMID 11007341

131. Muller M et al. Inhibition of the human erythrocytic

glutathione-S-transferase T1 (GST T1) by thimerosal. Int J Hyg

Environ Health 2001 203(5-6):479-81. PMID 11556154

132. Corrales F et al. Inhibition of glutathione synthesis in the

liver leads to S-adenosyl-L-methionine synthetase reduction.

Hepatology 1991 14(3):528-33. PMID 1874498

[Note etiologic connection with thimerosal and methionine synthase,

cite 20]

133. Pajares MA et al. Modulation of rat liver S-adenosylmethionine

synthetase activity by glutathione. J Biol Chem 1992 267(25):17598-

605. PMID 1517209

http://www.jbc.org/cgi/reprint/267/25/17598.pdf

[Note etiologic connection with thimerosal and methionine synthase,

cite 20]

134a. Meister A et al. Intracellular cysteine and glutathione

delivery systems. J Am Coll Nutr. 1986;5(2):137-51. PMID 3722629

134b. Jill & colleagues. Thimerosal Neurotoxicity is

Associated with Glutathione Depletion: Protection with Glutathione

Precursors. Neurotoxicology, in press 2004.

Chorioamnionitis, fetal, placental

135. Abruptio placentae and chorioamnionitis-microbiological and

histologic correlation. Acta Obstet Gynecol Scand. 1999 May;78

(5):363-6 PMID 10326877

" Conclusion: The incidence of silent chorioamnionitis (placental

membrane culture positivity) is higher in the abruptio placentae. "

136. Clinical chorioamnionitis, elevated cytokines, and brain injury

in term infants. Pediatrics. 2002 Oct;110(4):673-80 PMID 12359779

137. Fetal endothelial cells express vascular cell adhesion molecule

in the setting of chorioamnionitis. Am J Reprod Immunol 2000 43

(5):259-63 PMID 12359779

138. Chorioamnionitis and uterine function. Obstet Gynecol 2000;

95:909-12 PMID: 10831982

" Several small studies have suggested that chorioamnionitis has an

inhibitory effect upon labor, characterized by decreased uterine

contractility, decreased sensitivity to oxytocin stimulation, and

subnormal cervical dilation. " [3 cites]

139. Effect of amniotic fluid bacteria on the course of labor in

nulliparous women at term

Obstet Gynecol 68:587-592 1986 PMID: 3763067

[Nulliparous – no prior live births]

" Patients with intraamniotic infection have an increased rate of

cesarean delivery… These results support a causal relationship

between high-virulence bacteria in the amniotic fluid and poor

cervical dilation response to oxytocin… "

" Friedman… studied nulliparous patients with `amniotic infection

syndrome' and found that 70.5% had labor dysfunction. More recent

reports have confirmed this association and have also identified an

increased frequency of cesarean delivery among these women. "

" Koh et al… reported a 43% cesarean section rate in 140 patients

with clinical `chorioamnionitis.' "

" Two-thirds of the cesarean sections were performed because of poor

progress in labor despite the use of oxytocin… "

140. A fetal systemic inflammatory response is followed by the

spontaneous onset of preterm parturition. Am J Obstet Gynecol. 1998

Jul;179(1):186-93

141. Preeclampsia is associated with widespread apoptosis of

placental cytotrophoblasts within the uterine wall. Am J Pathol 1999

155(1):293-301 PMID 10393861

142. Maternal periodontal disease is associated with an increased

risk for preeclampsia.

Obstet Gynecol. 2003 Feb;101(2):227-31 PMID 12576243

Colic, cow's milk allergy in breast fed infants

143. Colic in breast-milk-fed infants: treatment by temporary

substitution of neocate infant formula. Acta Paediatr 2000 Jul;89

(7):795-802

144. Development of cow's milk allergy in breast-fed infants. Clin

Exp Allergy 2001 Jul;31(7):978-87

145. Cow's milk allergy in infancy. Curr Opin Allergy Clin Immunol.

2002 2(3):217-25

146. Cow's milk allergy presented with bloody stools from day 1 of

life. Eur J Pediatr. 2003 Mar;162(3):214-5

147. Host A. Frequency of cow's milk allergy in childhood. Ann

Allergy Asthma Immunol. 2002 Dec;89(6 Suppl 1):33-7. PMID: 12487202

148. Bahna SL. Cow's milk allergy versus cow milk intolerance. Ann

Allergy Asthma Immunol. 2002 Dec;89(6 Suppl 1):56-60. PMID: 12487206

149. Magazzu G, Scoglio R. Gastrointestinal manifestations of cow's

milk allergy. Ann Allergy Asthma Immunol. 2002 Dec;89(6 Suppl 1):65-

8. PMID: 12487208

149b. Iacono G et al. Severe infantile colic and food intolerance: a

long-term prospective study. J Pediatr Gastroenterol Nutr. 1991

Apr;12(3):332-5.

" To determine the relationship between infantile colic and cow's

milk protein intolerance (CMPI) in formula-fed infants, 70 infants

(38 male, 32 female) were selected, with mean age 30.2 ± 21.4 days,

with severe colic (duration of crying greater than 4 h per day for 5

days per week). In 50 of the infants in the study group (71.4%)

there was a remission of symptoms when cow's milk protein (CMP) was

eliminated from the diet. Two successive challenges caused the

return of symptoms in all these 50 infants. There was a positive

anamnesis for atopy in 9 of 50 of the patients with CMP-related

colic and in 1 of 20 of those with non-CMP-related colic (p greater

than 0.05). A follow-up period of 18 months' mean duration showed

that 22 of 50 (44%) of the infants with CMP-related colic and 1 of

20 (5%) of those with non-CMP-related colic developed an overt

alimentary intolerance (p less than 0.02). We conclude that a

considerable percentage of the infants with severe colic also have

CMPI and that in these cases, dietetic treatment should be the first

therapeutic approach. "

Chronic Diarrhea of Infancy

150. Chronic protracted diarrhea of infancy: a nutritional disease.

Pediatrics. 1983 Dec;72(6):786-800. PMID 6417622

151. Pathogenesis of small-intestinal mucosal lesions in chronic

diarrhea of infancy: I. A light microscopic study. J Pediatr

Gastroenterol Nutr. 1990 Nov;11(4):455-63. PMID: 2262834

152. Pathogenesis of small-intestinal mucosal lesions in chronic

diarrhea of infancy: II. An electron microscopic study. J Pediatr

Gastroenterol Nutr 1990 11(4):464-80 PMID 2262835

153. Mehta DI, Blecker U. Chronic diarrhea in infancy and childhood.

J La State Med Soc. 1998 Sep;150(9):419-29. PMID 9785754

Recurrent otitis

154. Recent advances in otitis media. 6. Microbiology and

immunology. Ann Otol Rhinol Laryngol Suppl. 2002 188:62-81. PMID

11968862

155. Viral-Bacterial Synergy in Otitis Media: Implications for

Management. Curr Infect Dis Rep. 2000 Apr;2(2):154-159. PMID:

11095851

156. Chonmaitree T et al. Presence of cytomegalovirus and herpes

simplex virus in middle ear fluids from children with acute otitis

media. Clin Infect Dis 1992 15(4):650-3 PMID 1330014

157. The common mucosal immune system and current strategies for

induction of immune responses in external secretions. J Clin

Immunol. 1987 Jul;7(4):265-76. PMID: 3301884

158. IgA antibody-producing cells in peripheral blood after antigen

ingestion: evidence for a common mucosal immune system in humans.

Proc Natl Acad Sci U S A. 1987 Apr;84(8):2449-53. PMID: 3470804

159. Management of chronic otitis media with effusion: the role of

glutathione. Laryngoscope. 2001 Aug;111(8):1486-9. PMID: 11568588

" BACKGROUND: The inflammatory cells documented in chronic otitis

media with effusion (OME) spontaneously release oxidants which can

induce middle ear (ME) epithelial cell damage. Glutathione (GSH), a

major extracellular antioxidant in humans, plays a central role in

antioxidant defense. PURPOSE: To evaluate the effects of GSH

treatment on chronic otitis media with effusion (OME). SUBJECTS AND

INTERVENTION: Sixty children with chronic OME were enrolled, 30 of

whom were randomly assigned to the treatment group and 30 to the

placebo group. Patients in the treatment group received 600 mg

glutathione in 4 mL saline per day subdivided into five 2-minute

administrations given by nasal aerosol every 3 or 4 waking hours for

2 weeks. Patients in the control group received 4 mL saline per day

following the same procedure as for GSH treatment. RESULTS: Three

months after therapy improvement had occurred in 66.6% of patients

in the GSH-treated group and in 8% of the control subjects (P <.01).

CONCLUSION: On the basis of these results, GSH treatment could be

considered for the nonsurgical management of chronic OME. "

160. Cow's milk allergy is associated with recurrent otitis media

during childhood. Acta Otolaryngol. 1999;119(8):867-73. PMID 10728925

Gluten hypersensitivity

161. Frick TJ, Olsen WA. Celiac disease and the spectrum of gluten

sensitivity. Gastroenterologist. 1994 Dec;2(4):285-92. PMID:

7866735

" Celiac disease is a well-known entity in which intolerance to wheat

gluten and related proteins from barley, rye, and oats (collectively

known as prolamins) damage intestinal mucosa. New insights into the

pathology of the celiac intestinal lesion point to a wider spectrum

of gluten sensitivity than previously thought. Recent advances in

immunology and genetics have shed light on the underlying mechanisms

and risks associated with the disease. Although the classical

manifestations are well known, the wide variety of clinical

presentations make celiac disease often difficult to diagnose, and

the ubiquitous presence of prolamins in the Western diet make

treatment challenging.

162. Fasano A, Catassi C. Current approaches to diagnosis and

treatment of celiac disease: an evolving spectrum. Gastroenterology

2001 120(3):636-51. PMID: 11179241

" Celiac disease (CD) is a syndrome characterized by damage of the

small intestinal mucosa caused by the gliadin fraction of wheat

gluten and similar alcohol-soluble proteins (prolamines) of barley

and rye in genetically susceptible subjects. The presence of gluten

in these subjects leads to self-perpetuating mucosal damage, whereas

elimination of gluten results in full mucosal recovery. The clinical

manifestations of CD are protean in nature and vary markedly with

the age of the patient, the duration and extent of disease, and the

presence of extraintestinal pathologic conditions. In addition to

the classical gastrointestinal form, a variety of other clinical

manifestations of the disease have been described, including

atypical and asymptomatic forms. Therefore, diagnosis of CD is

extremely challenging and relies on a sensitive and specific

algorithm that allows the identification of different manifestations

of the disease. Serologic tests developed in the last decade provide

a noninvasive tool to screen both individuals at risk for the

disease and the general population… "

163. Catassi C, Fabiani E. The spectrum of coeliac disease in

children. Baillieres Clin Gastroenterol. 1997 Sep;11(3):485-507.

PMID: 9448912

" Coeliac disease is the life-long intolerance to dietary gluten,

usually characterized by severe damage to the small-intestinal

mucosa. The widespread use of sensitive diagnostic tools, such as

the serum anti-gliadin and the anti-endomysial antibodies, has shown

not only that coeliac disease is one of the commonest disorders in

Western countries but also that this condition is characterized by a

higher degree of clinical variability than previously thought

(typical, atypical and silent forms). The existence of a latent-

potential coeliac disease and even a gluten-sensitive disease with

immunological activation of an otherwise normal small-intestinal

mucosa has recently been postulated. An increased prevalence of

coeliac disease in a number of other disorders has also been

reported in both children and adults. The reasons for such a wide

clinical heterogeneity are still poorly understood but are likely to

depend on both genetic and environmental factors. Further

investigations are required to evaluate the impact of undiagnosed,

clinically milder forms of coeliac disease on the well-being of the

population. "

164. Murray JA. The widening spectrum of celiac disease. Am J Clin

Nutr. 1999 Mar;69(3):354-65.

http://www.ajcn.org/cgi/reprint/69/3/354.pdf

165. Sollid LM, Gray GM. A role for bacteria in celiac disease? Am J

Gastroenterol. 2004 May;99(5):905-6. {Comment on: Am J

Gastroenterol. 2004 May;99(5):894-904.} PMID: 15128358

" The finding of rod-shaped bacteria attached to the small intestinal

epithelium of some untreated and treated celiac-disease patients,

but not to the epithelium of healthy controls, ignites the notion

that bacteria may be involved in the pathogenesis of celiac disease.

This editorial discusses this possibility in relation to the current

understanding of the molecular basis of this disorder.

166: Forsberg G et al. Presence of bacteria and innate immunity of

intestinal epithelium in childhood celiac disease. Am J

Gastroenterol. 2004 May;99(5):894-904. PMID: 15128357

167. Tursi A et al. High prevalence of small intestinal bacterial

overgrowth in celiac patients with persistence of gastrointestinal

symptoms after gluten withdrawal. Am J Gastroenterol. 2003 Apr;98

(4):839-43. PMID: 12738465

" OBJECTIVE: Celiac disease is a gluten-sensitive enteropathy with a

broad spectrum of clinical manifestation, and most celiac patients

respond to a gluten-free diet (GFD). However, in some rare cases

celiacs continue to experience GI symptoms after GFD, despite

optimal adherence to diet. The aim of our study was to evaluate the

causes of persistence of GI symptoms in a series of consecutive

celiac patients fully compliant to GFD. METHODS: We studied 15

celiac patients (five men, 10 women, mean age 36.5 yr, range 24-59

yr) who continued to experience GI symptoms after at least 6-8

months of GFD (even if of less severity). Antigliadin antibody (AGA)

test, antiendomysial antibody (EMA) test, and sorbitol H2-breath

test (H2-BT), as well as sophagogastroduodenoscopy (EGD) with

histological evaluation, were performed before starting GFD. Bioptic

samples were obtained from the second duodenal portion during EGD,

and histopathology was expressed according to the Marsh

classification. To investigate the causes of persistence of GI

symptoms in these patients, we performed AGA and EMA tests, stool

examination, EGD with histological examination of small bowel

mucosa, and sorbitol-, lactose-, and lactulose H2-breath tests.

RESULTS: Histology improved in all patients after 6-8 months of GFD;

therefore, refractory celiac disease could be excluded. One patient

with Marsh II lesions was fully compliant to his diet but had

mistakenly taken an antibiotic containing gluten. Two patients

showed lactose malabsorption, one patient showed Giardia lamblia and

one patient Ascaris lumbricoides infestation, and 10 patients showed

small intestinal bacterial overgrowth (SIBO) by lactulose H2-BT. We

prescribed a diet without milk or fresh milk-derived foods to the

patient with lactose malabsorption; we treated the patients with

parasite infestation with mebendazole 500 mg/day for 3 days for 2

consecutive wk; and we treated the patients with SIBO with rifaximin

800 mg/day for 1 wk. The patients were re-evaluated 1 month after

the end of drug treatment (or after starting lactose-free diet); at

this visit all patients were symptom-free. CONCLUSIONS: This study

showed that SIBO affects most celiacs with persistence of GI

symptoms after gluten withdrawal.

168. Wheat allergy: clinical and laboratory findings. Int Arch

Allergy Immunol. 2004 Feb;133(2):168-73. PMID: 14764944

169a. Hadjivassiliou M et al. Does cryptic gluten sensitivity play

a part in neurological illness? Lancet. 1996 Feb 10;347(8998):369-

71. PMID: 8598704

BACKGROUND: Antigliadin antibodies are a marker of untreated coeliac

disease but can also be found in individuals with normal small-bowel

mucosa. Because neurological dysfunction is a known complication of

coeliac disease we have investigated the frequency of antigliadin

antibodies, as a measure of cryptic gluten sensitivity, and coeliac

disease in neurological patients. METHODS: Using ELISA, we estimated

serum IgG and IgA antigliadin antibodies in 147 neurological

patients who were divided into two groups. There were 53 patients

with neurological dysfunction of unknown cause despite full

investigation (25 ataxia, 20 peripheral neuropathy, 5 mononeuritis

multiplex, 4 myopathy, 3 motor neuropathy, 2 myelopathy). The

remaining 94 patients were found to have a specific neurological

diagnosis (16 stroke, 12 multiple sclerosis, 10 Parkinson's disease,

56 other diagnoses) and formed the neurological control group. 50

healthy blood donors formed a third group. FINDINGS: The proportions

of individuals with positive titres for antigliadin antibodies in

the three groups were 30/53, 5/94, and 6/50 respectively (57, 5, and

12%). The difference in proportion between group 1 and the combined

control groups was 0.49 (95% CI 0.35-0.63). Distal duodenal biopsies

in 26 out of 30 antigliadin-positive patients from group 1 revealed

histological evidence of coeliac disease in nine (35%), non-specific

duodenitis in ten (38%), and no lesion in seven (26%) individuals.

INTERPRETATION: Our data suggest that gluten sensitivity is common

in patients with neurological disease of unknown cause and may have

aetiological significance.

169b. Dietary treatment of gluten ataxia. J Neurol Neurosurg

Psychiatry. 2003 Sep;74(9):1221-4. PMID: 12933922

m.hadjivassiliou@...

http://jnnp.bmjjournals.com/cgi/reprint/74/9/1221.pdf

BACKGROUND: Gluten ataxia is an immune mediated disease, part of the

spectrum of gluten sensitivity, and accounts for up to 40% of cases

of idiopathic sporadic ataxia. No systematic study of the effect of

gluten-free diet on gluten ataxia has ever been undertaken.

OBJECTIVE: To study the effect of gluten-free diet on patients

presenting with ataxia caused by gluten sensitivity. METHODS: 43

patients with gluten ataxia were studied. All were offered a gluten-

free diet and monitored every six months. All patients underwent a

battery of tests to assess their ataxia at baseline and after one

year on diet. Twenty six patients (treatment group) adhered to the

gluten-free diet and had evidence of elimination of antigliadin

antibodies by one year. Fourteen patients refused the diet (control

group). Three patients had persistently raised antigliadin

antibodies despite adherence to the diet and were therefore excluded

from the analysis. RESULTS: After one year there was improvement in

ataxia reflected in all of the ataxia tests in the treatment group.

This was significant when compared with the control group. The diet

associated improvement was apparent irrespective of the presence of

an enteropathy. CONCLUSIONS: Gluten ataxia responds to a strict

gluten-free diet even in the absence of an enteropathy. The

diagnosis of gluten ataxia is vital as it is one of the very few

treatable causes of sporadic ataxia.

170. Food allergy to wheat: identification of immunogloglin E and

immunoglobulin

G-binding proteins with sequential extracts and purified proteins

from wheat flour. Clin Exp Allergy. 2003 Jul;33(7):962-70. PMID:

12859454

171. Update on wheat hypersensitivity. Curr Opin Allergy Clin

Immunol. 2003 Jun;3(3):205-9. PMID: 12840704

Gluten neuropathologies

172: li M et al. Association between migraine and Celiac

disease: results from a preliminary case-control and therapeutic

study. Am J Gastroenterol. 2003 Mar;98(3):625-9. PMID: 12650798

" OBJECTIVES: Subclinical celiac disease (CD) has been associated

with various neurological disorders, the most common being

neuropathy and cerebellar ataxia. The aims of the present study were

to assess the following: 1) the prevalence of CD in patients

affected by migraine; 2) whether there are regional cerebral blood

flow abnormalities in migraine patients with CD compared to migraine

patients without CD; and 3) the effects of a gluten free diet in

migraine patients with CD. METHODS: A total of 90 patients affected

by idiopathic migraine were enrolled, and 236 blood donors were used

as controls. Serum IgG antitransglutaminase (TgA) and IgA

antiendomysial (EmA) were measured. In positive cases, diagnosis was

confirmed endoscopically. A gluten free diet was started in the

patients diagnosed with CD, who were followed for 6 months. A single

photon emission CT brain study was performed before and after a

gluten free diet. RESULTS: Four of 90 (4.4%; 95% CI = 1.2-11.0)

migraine patients were found to have CD compared with 0.4% (95% CI =

0.01-2.3) blood donor controls (p < 0.05). During the 6 months of

gluten free diet, one of the four patients had no migraine attacks,

and the remaining three patients experienced an improvement in

frequency, duration, and intensity of migraine. Single photon

emission CT studies showed a regional baseline reduction in brain

tracer uptake in all four patients. Such reduction in uptake

completely resolved at follow-up. CONCLUSIONS: Our results suggest

that a significant proportion of patients with migraine may have CD,

and that a gluten free diet may lead to a improvement in the

migraine in these patients.

173. Gluten sensitivity as a neurological illness. J Neurol

Neurosurg Psychiatry. 2002 May;72(5):560-3. PMID: 11971034

http://jnnp.bmjjournals.com/cgi/reprint/72/5/560.pdf

174. Headache and CNS white matter abnormalities associated with

gluten sensitivity. Neurology 2001 13;56(3):385-8

" The authors describe 10 patients with gluten sensitivity and

abnormal MRI. All experienced episodic headache, six had

unsteadiness, and four had gait ataxia. MRI abnormalities varied

from confluent areas of high signal throughout the white matter to

foci of high signal scattered in both hemispheres. Symptomatic

response to gluten-free diet was seen in nine patients. "

175. De Santis A et al. Schizophrenic symptoms and SPECT

abnormalities in a coeliac patient: regression after a gluten-free

diet. J Intern Med. 1997 Nov;242(5):421-3. PMID: 9408073

" A 33-year-old patient, with pre-existing diagnosis

of 'schizophrenic' disorder, came to our observation for severe

diarrhoea and weight loss. Use of single photon emission computed

tomography, (99mTc)HMPAO SPECT, demonstrated hypoperfusion of the

left frontal brain area, without evidence of structural cerebral

abnormalities. Jejunal biopsy showed villous atrophy. Antiendomysial

antibodies were present. A gluten-free diet was started, resulting

in a disappearence of psychiatric symptoms, and normalization of

histological duodenal findings and of (99mTc)HMPAO SPECT pattern.

This is the first case in which, in an undiagnosed and untreated

coeliac patient with psychiatric manifestations, the (99mTc)HMPAO

SPECT demonstrated a dysfunction of frontal cortex disappearing

after a gluten-free diet.

176. Usai P et al. Frontal cortical perfusion abnormalities related

to gluten intake and associated autoimmune disease in adult coeliac

disease: 99mTc-ECD brain SPECT study. Dig Liver Dis. 2004 Aug;36

(8):513-8. PMID: 15334770

OBJECTIVE: Since brain perfusion abnormalities have been described

by single-photon emission computed tomography in some autoimmune

diseases, the aim of the present study was to evaluate the incidence

of perfusion abnormalities by brain single-photon emission computed

tomography in a group of coeliac disease patients, and to

investigate whether gluten intake and associated autoimmune diseases

may be considered risk factors in causing cerebral impairment.

METHODS: Thirty-four adult coeliac patients (16 on a gluten-free

diet and 18 on a gluten-containing diet, 18 (53%) with autoimmune

diseases) underwent 99mTc-ethyl cysteinate dimer brain single-photon

emission computed tomography and qualitative evaluation of brain

perfusion was performed together with a semiquantitative estimation

using the asymmetry index. Ten subjects on our database, matched for

sex, age and ethnic group, who were proved normal by histology of

jejunal mucosa (four males and six females; median age 39 years,

range 27-55 years), were included as control group. RESULTS: Twenty-

four out of 34 patients (71%) showed brain single-photon emission

computed tomography abnormalities confirmed by abnormal regional

asymmetry index (>5%; range 5.8-18.5%). Topographic comparison of

the brain areas showed that the more significant abnormalities were

localised in frontal regions, and were significantly different from

controls only in coeliac disease patients on unrestricted diet. The

prevalence of single-photon emission computed tomography

abnormalities was similar in coeliac disease patients with (74%) and

without (69%) associated autoimmune disease. CONCLUSIONS:

Abnormalities of brain perfusion seem common in coeliac disease.

This phenomenon is similar to that previously described in other

autoimmune diseases, but does not appear to be related to associated

autoimmunity and, at least in the frontal region, may be improved by

a gluten-free diet.

Gluten immunologics

177. The humoral response in the pathogenesis of gluten ataxia.

Neurology 2002 Apr 23;58(8):1221-6

" The authors assessed the reactivity of sera from patients with

gluten ataxia (13), newly diagnosed patients with celiac disease

without neurologic dysfunction (24), patients with other causes of

cerebellar degeneration (11), and healthy control subjects (17).

" Sera from 12 of 13 patients with gluten ataxia stained Purkinje

cells strongly. Less intense staining was seen in some but not all

sera from patients with newly diagnosed celiac disease without

neurologic dysfunction. At high dilutions (1:800) staining was seen

only with sera from patients with gluten ataxia but not in control

subjects. Sera from patients with gluten ataxia also stained some

brainstem and cortical neurons in rat CNS tissue. Commercial anti-

gliadin antibody stained human Purkinje cells in a similar manner…

Patients with gluten ataxia have antibodies against Purkinje cells.

Antigliadin antibodies cross-react with epitopes on Purkinje cells. "

178. Jarvinen TT et al. Intraepithelial lymphocytes in celiac

disease. Am J Gastroenterol. 2003 Jun;98(6):1332-7. PMID: 12818278

OBJECTIVE: The aim of this study was to investigate the value of

immunohistochemical characterization of different intraepithelial

lymphocytes (IELs) in the diagnostic workup of celiac disease (CD).

METHODS: The study involved 928 consecutive adult patients

undergoing endoscopy undertaken on suspicion of CD or to ascertain

the dietary compliance; the control group consisted of 59 adults who

underwent endoscopy because of indigestion. Small bowel mucosal

morphology, CD3+, alphabeta+, and gammadelta+ IELs were determined.

RESULTS: CD was detected in 138 and excluded in 545 adults. CD3+ and

gammadelta+ IELs both showed a sensitivity of 93% for CD;

specificity was 73% and 88%, respectively. For alphabeta+ cells, the

sensitivity was 83% and specificity, 66%. The mucosal morphology

recovered on a gluten-free diet and the densities of different IELs,

even gammadelta+ cells, decreased. Only the density of gammadelta+

cells remained elevated compared with controls. CONCLUSIONS:

Counting of IELs is recommended in borderline cases where the

histology is difficult to interpret. An increase especially in

gammadelta+ cells strengthens the probability of CD. However, IELs

are not invariably increased in CD.

179. Cataldo F et al. Cytokine genotyping (TNF and IL-10) in

patients with celiac disease and selective IgA deficiency. Am J

Gastroenterol. 2003 Apr;98(4):850-6. PMID: 12738467

" OBJECTIVE: Selective IgA deficiency (IgAD) and celiac disease (CD)

are frequently associated and share the ancestral haplotype human

leukocyte antigen (HLA)-8.1, which is characterized by a peculiar

cytokine profile. The aim of this study was to evaluate the role of

tumor necrosis factor (TNF) and interleukin (IL)-10 alleles in CD

and CD-IgAD… CONCLUSIONS: Genetically determined increased

production of TNF-alpha and reduction of IL-10 may be relevant for

susceptibility to CD, mainly in IgAD, as the different allele

expression at TNF and IL-10 loci seems to influence cytokine

production profile.

180. Esposito C et al. Expression and enzymatic activity of small

intestinal tissue transglutaminase in celiac disease. Am J

Gastroenterol. 2003 Aug;98(8):1813-20. PMID: 12907337

" Tissue transglutaminase is more expressed and active in defined

areas of the small intestinal mucosa from patients with CD. The

presence in the celiac mucosa of proteins able to act as amine-donor

substrates suggests that tissue transglutaminase-mediated post-

translational modification of proteins cross-linked with gliadin

peptides may represent a pathogenic mechanism of CD. "

181. Liu E et al. Fluctuating transglutaminase autoantibodies are

related to histologic features of celiac disease. Clin Gastroenterol

Hepatol. 2003 Sep;1(5):356-62. PMID: 15017653

" BACKGROUND & AIMS: Asymptomatic children at risk for celiac disease

(CD) and seropositive for immunoglobulin A anti-TG autoantibodies

(TGAA) may lack small intestinal mucosal changes characteristic of

CD. We have followed a group of children with serial testing for

TGAA… CONCLUSIONS: In children with TGAA seropositivity, the TGAA

level varied over time and a higher titer predicted an abnormal

biopsy characteristic of CD. A threshold for biopsy for diagnosis of

CD could be set higher for screening-identified cases than for

clinically identified cases to decrease the frequency of

performing " normal " biopsies.

Chelation

182: Lonsdale D, Shamberger RJ, Audhya T. Treatment of autism

spectrum children with thiamine tetrahydrofurfuryl disulfide: a

pilot study. Neuroendocrinol Lett. 2002 Aug;23(4):303-8. PMID:

12195231 dlonsdale@...

" OBJECTIVES: In a Pilot Study, the clinical and biochemical effects

of thiamine tetrahydrofurfuryl disulfide (TTFD) on autistic spectrum

children were investigated. SUBJECTS AND METHODS: Ten children were

studied. Diagnosis was confirmed through the use of form E2, a

computer assessed symptom score. For practical reasons, TTFD was

administered twice daily for two months in the form of rectal

suppositories, each containing 50 mg of TTFD. Symptomatic responses

were determined through the use of the computer assessed Autism

Treatment Evaluation Checklist (ATEC) forms. The erythrocyte

transketolase (TKA) and thiamine pyrophosphate effect (TPPE), were

measured at outset and on completion of the study to document

intracellular thiamine deficiency. Urines from patients were

examined at outset, after 30 days and after 60 days of treatment and

the concentrations of SH-reactive metals, total protein, sulfate,

sulfite, thiosulfate and thiocyanate were determined. The

concentrations of metals in hair were also determined. RESULTS: At

the beginning of the study thiamine deficiency was observed in 3 out

of the 10 patients. Out of 10 patients, 6 had initial urine samples

containing arsenic in greater concentration than healthy controls.

Traces of mercury were seen in urines from all of these autistic

children. Following administration of TTFD an increase in cadmium

was seen in 2 children and in lead in one child. Nickel was

increased in the urine of one patient during treatment. Sulfur

metabolites in urine did not differ from those measured in healthy

children. CONCLUSIONS: Thiamine tetrahydrofurfuryl disulfide appears

to have a beneficial clinical effect on some autistic children,

since 8 of the 10 children improved clinically. We obtained evidence

of an association of this increasingly occurring disease with

presence of urinary SH-reactive metals, arsenic in particular. "

182. Lonsdale presentation to DAN! 2003, Philadelphia

http://64.202.182.52/powerpoint/dan2003/Lonsdale.htm

183. A. Holmes, S. Cave, and J.M. El-Dahr. OPEN TRIAL OF CHELATION

WITH MES0-2,3-DIMERCAPTO SUCCINIC ACID (DMSA) AND LIPOIC ACID (LA)

IN CHILDREN WITH AUTISM. As submitted to IMFAR, June 2, 2001.

" Over 400 patients with autism are currently undergoing treatment

for removal of heavy metals. Patients are treated with DMSA alone at

doses of 10 mg/kg/dose 3 times a day for 3 days in a row (shorter

duration than lead protocol to decrease side effects) with 11

days " off " to allow metals to re-equilibrate. After at least 2

rounds of DMSA alone, the thiol antioxidant lipoic acid

(hypothesized to aide in removal of heavy metals across the BBB)is

added to each dose of DMSA at 2-3mg/kg/dose. In general, noticeable

improvements in language, self-help skills, interaction, and core

autistic features are not seen until the patient has been on DMSA

with LA for 2-3 months.

" Of patients who have been on DMSA/LA for at least 4 months, these

results have been noted on general global assessment by parents,

teachers, and MDs: age 1-5yrs(n=40): marked improvement 35%,

moderate 39%, slight 15%, none 11%; age 6-12yrs (n=25): marked 4%,

moderate 28%, slight 52%, none 16%; age 13-17 (n=16): moderate 6%,

slight 68%, none 26%; age 18+ (n=4): slight 25%, none 75%. For

example, a boy 5yr 5mo scored in the average range on a one word

expressive vocabulary test 10/00 and at age equivalent 8yr 2mo in

3/01 with no change in education or medication other than starting

DMSA/LA.

" The majority of children excrete mercury, lead, and other metals,

suggesting that there may be a generalized problem with metal

metabolism. Side effects include transient increases in

hyperactivity, self-stimulatory behavior, and loose stools. Younger

children in particular respond well to this therapy with significant

improvement in function. "

184. DMSA Chelation efficacy PPT presentation by Jane El-Dahr, M.D.

185. Excellent DAN! PPT Presentations online

http://www.autismresearchinstitute.com/dan/dan.htm

186. Lead poisoning treatment--a continuing need (commentary). J

Toxicol Clin Toxicol. 2001;39(7):661-3. PMID: 11778663

187. Lightening the lead load in children. Am Fam Physician 2000 62

(3):545-54, 559-60 PMID: 10950212

188. Mercury poisoning. Curr Probl Pediatr. 2000 Mar;30(3):91-9.

PMID: 10742922

189. Lead poisoning in children. Curr Opin Pediatr. 1997 Apr;9

(2):173-7. PMID: 9204246

190. Lead intoxication in children with pervasive developmental

disorders. J Toxicol Clin Toxicol. 1996;34(2):177-81. PMID: 8618251

191. Pediatric arsenic ingestion. Am J Emerg Med. 1995 Jul;13(4):432-

5. PMID: 7605532

192. Oral chelators for childhood lead poisoning. Pediatr Ann. 1994

23(11):616-9, 623-6. PMID: 7838614

193. Succimer: the first approved oral lead chelator.Am Fam

Physician. 1993 Dec;48(8):1496-502. PMID: 8249780

194. The current role of 2,3-dimercaptosuccinic acid (DMSA) in the

management of childhood lead poisoning.Drug Saf. 1993 Aug;9(2):85-

92. PMID: 8397892

Viruses in autism

195. Ghaziuddin M et al. Autistic symptoms following herpes

encephalitis. Eur Child Adolesc Psychiatry. 2002 Jun;11(3):142-6.

PMID: 12369775

" Autism is a childhood onset neurodevelopmental disorder

characterized by reciprocal social deficits, communication

impairment, and rigid ritualistic interests, with the onset almost

always before three years of age. Although the etiology of the

disorder is strongly influenced by genes, environmental factors are

also important. In this context, several reports have described its

association with known medical conditions, including infections

affecting the central nervous system. In this report, we describe an

11-year-old Asian youngster who developed the symptoms of autism

following an episode of herpes encephalitis. In contrast to previous

similar reports, imaging studies suggested a predominant involvement

of the frontal lobes. At follow-up after three years, he continued

to show the core deficits of autism. This case further supports the

role of environmental factors, such as infections, in the etiology

of autism, and suggests that in a minority of cases, autistic

symptoms can develop in later childhood.

196. Gillberg IC. Autistic syndrome with onset at age 31 years:

herpes encephalitis as a possible model for childhood autism. Dev

Med Child Neurol. 1991 Oct;33(10):920-4. PMID: 1743418

197. DeLong GR et al. Acquired reversible autistic syndrome in acute

encephalopathic illness in children. Arch Neurol. 1981 Mar;38

(3):191-4. PMID: 6162440

" In seeking the neurologic substrate of the autistic syndrome of

childhood, previous studies have implicated the medial temporal lobe

or the ring of mesolimbic cortex located in the mesial frontal and

temporal lobes. During an acute encephalopathic illness, a clinical

picture developed in three children that was consistent with

infantile autism. This development was reversible. It was

differentiated from acquired epileptic aphasia, and the language

disorder was differentiated aphasia. One child has rises in serum

herpes simplex titers, and a computerized tomographic (CT) scan

revealed an extensive lesion of the temporal lobes, predominantly on

the left. The other two, with similar clinical syndromes, had normal

CT scans, and no etiologic agent was defined. These cases are

examples of an acquired and reversible autistic syndrome in

childhood, emphasizing the clinical similarities to bilateral medial

temporal lobe disease as described in man, including the Kluver-Bucy

syndrome seen in postencephalitic as well as postsurgical states.

198. Gillberg C. Onset at age 14 of a typical autistic syndrome. A

case report of a girl with herpes simplex encephalitis. J Autism Dev

Disord. 1986 Sep;16(3):369-75. PMID: 3558293

199. Stubbs EG et al. Autism and congenital cytomegalovirus. J

Autism Dev Disord. 1984 Jun;14(2):183-9. PMID: 6086566

200. Ivarsson SA et al. Autism as one of several disabilities in two

children with congenital cytomegalovirus infection. Neuropediatrics.

1990 May;21(2):102-3. PMID: 2163029

201. McLachlan RS et al. Treatment of Rasmussen's syndrome with

ganciclovir. Neurology. 1996 Oct;47(4):925-8. PMID: 8857720

" Since cytomegalovirus (CMV) has been implicated in the pathogenesis

of Rasmussen's syndrome, we treated four patients with ganciclovir,

a potent anti-CMV drug. A 7-year-old girl with seizures escalating

to 60/day over 3 months despite triple antiepileptic drug therapy

became seizure-free 5 days after initiation of treatment with no

recurrence at 1.5 years follow-up. Focal neurologic signs, cognitive

function, and the EEG returned to normal. Two patients treated 34

and 72 months after disease onset in association with epilepsy

surgery had a reduction in seizures and one had no response. CMV

genome was detected in the brains of two of the three patients in

whom it was assessed. The response to antiviral therapy supports a

viral etiology for chronic encephalitis of Rasmussen. If the disease

is suspected, treatment with ganciclovir should be considered as

early as possible.

202. Domachowske JB et al. Acute manifestations and neurologic

sequelae of Epstein-Barr virus encephalitis in children. Pediatr

Infect Dis J. 1996 Oct;15(10):871-5. PMID: 8895918

BACKGROUND: Complications of Epstein-Barr virus (EBV) infection are

diverse and include a number of neurologic manifestations such as

meningitis, meningoencephalitis, cerebellitis, cranial neuritis and

others. In general encephalitis caused by EBV in pediatric patients

has been considered a self-limited illness with few or no sequelae.

METHODS: Charts were reviewed from all patients < 18 years of age

admitted to or discharged from the State University of New York

Health Science Center at Syracuse between 1982 and 1992 with a

diagnosis of encephalitis or meningo- encephalitis. Eleven cases of

EBV encephalitis diagnosed during a 10-year period were reviewed to

characterize the clinical and laboratory findings in the acute

setting and the extent of neurologic sequelae on follow-up. RESULTS:

Acute neurologic manifestations were diverse and included combative

behavior (55%), seizures (36%), headache (36%) and evidence of focal

involvement (27%). Classic findings of infectious mononucleosis were

noted infrequently; 18% each had pharyngitis, adenopathy, positive

heterophile antibody tests or atypical lymphocytosis. Two patients

(18%) had abnormal neuroimaging studies, one in the acute stage and

the other at the time of follow-up. Seven patients (64%) had

abnormal electroencephalograms (EEGs) in the acute setting; of these

three had persistent abnormalities on follow-up. Forty percent

developed persistent neurologic abnormalities including global

impairment, perseverative autistic-like behavior and persistent left

upper extremity paresis. CONCLUSIONS: Classic signs, symptoms and

laboratory findings in infectious mononucleosis may be absent in

Epstein-Barr virus encephalitis. Neurologic sequelae occur in a

substantial number of patients.

203. Caruso JM et al. Persistent preceding focal neurologic deficits

in children with chronic Epstein-Barr virus encephalitis. J Child

Neurol. 2000 Dec;15(12):791-6. PMID: 11198493

" Epstein-Barr virus encephalitis is a self-limiting disease with few

sequelae. Persistence of neurologic deficits prior to and after the

acute illness has yet to be described in children. We describe five

children with persistent cognitive and focal neurologic deficits due

to chronic Epstein-Barr virus encephalitis with various T2-weighted

magnetic resonance imaging abnormalities. Clinical features were a 9-

year-old boy with aphasia and apraxia, an 11-year-old girl with

impulsivity and inappropriate behavior, a 17-year-old boy with

deterioration of cognitive skills and judgment, a 5-year-old boy

with complex-partial seizures, and a 6-year-old girl with obsessive-

compulsive behavior. All patients had elevated serum Epstein-Barr

virus titers for acute infection, with cerebrospinal fluid

polymerase chain reaction positive for Epstein-Barr virus in four

patients. Three children were treated with methylprednisolone with

minimal improvement without changes on magnetic resonance imaging.

Epstein-Barr virus encephalitis can present with chronic and

insidious neurologic symptoms and should be considered in the

differential diagnosis of children with acute or chronic neurologic

illness of unknown etiology. "

Probiotics

204. Erdeve O et al. The probiotic effect of Saccharomyces

boulardii in a pediatric age group. J Trop Pediatr. 2004 Aug;50

(4):234-6. PMID: 15357564

" The aim of this study was to determine the efficacy of S. boulardii

in diarrhea associated with commonly used antibiotics such as

sulbactam-ampicillin (SAM) and azithromycin (AZT). Four hundred and

sixty-six patients were assigned to four different groups as

follows: group 1:117 patients receiving SAM alone; group 2:117

patients receiving SAM and S. boulardii, group 3:105 patients

receiving AZT alone; group 4:127 patients receiving AZT and S.

boulardii. Antibiotic-associated diarrhea was seen in 42 of the 222

patients (18.9 per cent) receiving an antibiotic without the

probiotic, and in 14 of the 244 patients (5.7 per cent) who received

both the probiotic and the antibiotic (p < 0.05). In the group

receiving SAM where S. boulardii use was found to be significant,

the use of S. boulardii decreased the diarrhea rate from 32.3 to

11.4 per cent in the 1-5 years age group (p < 0.05). This is a

pioneering study investigating combined antibiotic and probiotic use

in pediatric diarrhea patients. "

205. Gill HS, Guarner F. Probiotics and human health: a clinical

perspective. Postgrad Med J. 2004 Sep;80(947):516-26. PMID:

15356352

" There is unequivocal evidence that administration of probiotics

could be effective in the treatment of acute infectious diarrhoea in

children and the prevention of antibiotic associated diarrhoea and

nosocomial/community acquired diarrhoea. Encouraging evidence is

also emerging for the effectiveness of probiotics in the prevention

and management of pouchitis and paediatric atopic diseases, and the

prevention of postoperative infections. There is also strong

evidence that certain probiotic strains are able to enhance immune

function, especially in subjects with less than adequate immune

function such as the elderly. Efficacy of probiotics in the

prevention of traveller's diarrhoea, sepsis associated with severe

acute pancreatitis, and cancers, the management of ulcerative

colitis, and lowering of blood cholesterol remains unproven. In

addition to firm evidence of efficacy (for a range of conditions),

major gaps exist in our knowledge regarding the mechanisms by which

probiotics modulate various physiological functions and the optimum

dose, frequency, and duration of treatment for different probiotic

strains. "

206. Kruis W. Antibiotics and probiotics in inflammatory bowel

disease. Aliment Pharmacol Ther. 2004 Oct;20 Suppl 4:75-8. PMID:

15352898

" Summary Treatment with antibiotics in inflammatory bowel disease

has a long tradition and is widely used. The indications for

antibiotic therapy are wide ranging, from specific situations such

as abscesses or fistulae, to patients with severe disease (as an

unspecific 'protective' measure), and to address the hypothesis that

the enteric flora as a whole, or specific microorganisms such as

mycobacteria, are involved in the pathogenesis of inflammatory bowel

disease. The best-studied single antibiotic compound is

metronidazole. However, overall, the scientific basis for the use of

antibiotics is limited, which may reflect a lack of interest from

sponsors within the pharmaceutical industry. Despite this weak

evidence base, antibiotics are a globally established therapeutic

tool in inflammatory bowel disease. Growing evidence from human and

animal studies points towards a pivotal pathogenetic role of

intestinal bacteria in inflammatory bowel disease. In view of these

experimental findings, clinical trials have been undertaken to

elucidate the therapeutic effects of probiotics in inflammatory

bowel disease. Probiotics are viable nonpathogenic microorganisms

which confer health benefits to the host by improving the microbial

balance of the indigenous microflora. So far, of the many

candidates, one specific strain (Escherichia coli Nissle 1917) and a

mixture of eight different bacteria have demonstrated convincing

therapeutic efficacy in controlled studies. Maintenance therapy in

ulcerative colitis and prevention therapy, as well as the treatment

of pouchitis, have emerged as areas in which probiotic therapy

offers a valid therapeutic alternative to current treatments.

Further investigations may detect additional clinically effective

probiotics and other clinical indications. "

207. Fedorak RN, Madsen KL. Probiotics and the management of

inflammatory bowel disease. Inflamm Bowel Dis. 2004 May;10(3):286-

99. PMID: 15290926

" The demonstration that immune and epithelial cells can discriminate

between different microbial species has extended our understanding

of the actions of probiotics beyond simple barrier and antimicrobial

concepts. Several probiotic mechanisms of action, relative to

inflammatory bowel disease, have been elucidated: (1) competitive

exclusion, whereby probiotics compete with microbial pathogens for a

limited number of receptors present on the surface epithelium; (2)

immunomodulation and/or stimulation of an immune response of gut-

associated lymphoid and epithelial cells; (3) antimicrobial activity

and suppression of pathogen growth; (4) enhancement of barrier

function; and (5) induction of T cell apoptosis in the mucosal

immune compartment. The unraveling of these mechanisms of action has

led to new support for the use of probiotics in the management of

clinical inflammatory bowel disease. Though level 1 evidence now

supports the therapeutic use of probiotics in the treatment of

postoperative pouchitis, only levels 2 and 3 evidence is currently

available in support of the use of probiotics in the treatment of

ulcerative colitis and Crohn's disease. Nevertheless, one

significant and consistent finding has emerged during the course of

research in the past year: not all probiotic bacteria have similar

therapeutic effects. Rigorously designed, controlled clinical trials

are vital to investigate the unresolved issues related to efficacy,

dose, duration of use, single or multi-strain formulation, and the

concomitant use of prebiotics, synbiotics, or antibiotics. "

208. Nardone G, Rocco A. Probiotics: a potential target for the

prevention and treatment of steatohepatitis. J Clin Gastroenterol.

2004 Jul;38(6 Suppl):S121-2. PMID: 15220676

" The accumulation of fat in hepatocytes with a necroinflammatory

component-steatohepatitis-that may or may not have associated

fibrosis is becoming a frequent lesion. Although steatohepatitis is

currently recognized to be a leading cause of cryptogenic cirrhosis,

the pathogenesis has not been fully elucidated. Among the various

factors implicated, intestinal bacterial overgrowth may play a role.

Indeed, various rat models of intestinal bacterial overgrowth have

been associated with liver lesions similar to NASH, and bacterial

overgrowth has been observed significantly more often in patients

with NASH compared with control subjects. The authors discuss the

relationship among intestinal bacterial overgrowth, steatohepatitis

development, and probiotic treatment. "

209. Saggioro A. Probiotics in the treatment of irritable bowel

syndrome. J Clin Gastroenterol. 2004 Jul;38(6 Suppl):S104-6. PMID:

15220671

" Irritable Bowel Syndrome (IBS) may be diagnosed on the presence of

symptoms, according to Rome II criteria and some studies have shown

that abnormal colonic fermentation may be an important factor in the

development of symptoms in some patients with IBS. Since the

fermentations of substrates by the intestinal flora may play a key

role in the use of probiotics in the treatment of IBS, fifty

patients (24 males, 26 females), mean age 40 years (range = 26-64

years) with IBS, according to Rome II criteria, were enrolled into

the study after informed consensus. Patients were randomly assigned

to receive either the active preparation containing Lactobacillus

Plantarum LP0 1 and Bifidocterium Breve BR0 both at a concentration

of 5 x 10 CFU/ml, or placebo powder containing starch identical to

the study product, for 4 weeks. To evaluate treatment efficacy two

different scores were considered: Pain score in different abdominal

locations after treatment decreased in probiotics group of 38%

versus 18% (P < 0.05) of placebo group after 14 days and of 52%

versus 11% (P < 0.001) after 28 days. The severity score of

characteristic IBD symptoms significantly decreased in probiotic

group versus placebo group after 14 days 49.6% versus 9.9% (P <

0.001) and these data were confirmed after 28 days (44.4% versus

8.5%, P < 0.001). In conclusion, short-term therapy with

Lactobacillus PlantarumLP0 1 and Bifidocterium Breve BR0 may be

considered a promising approach to the therapy for IBS. "

210. Di Stefano M et al. Probiotics and functional abdominal

bloating. J Clin Gastroenterol. 2004 Jul;38(6 Suppl):S102-3. PMID:

15220670

" Functional abdominal bloating is a condition dominated by a feeling

of abdominal fullness or bloating and without sufficient criteria

for another functional gastrointestinal disorder. The currently used

therapeutic approaches aim to reduce the volume of intestinal gas,

thus increasing intestinal gas elimination or reducing its

production. Some promising results have been obtained by the use of

prokinetics, such as tegaserod and Prostigmine, and by the use of

nonabsorbable antibiotics, such as rifaximin. Another therapeutic

approach is represented by the administration of probiotics to

modify the composition of colonic flora and thus the production of

intestinal gas. The authors recently studied the effect of LGG,

which proved to be more effective than placebo in reducing the

severity of symptoms. "

211. Isolauri E. Dietary modification of atopic disease: Use of

probiotics in the prevention of atopic dermatitis. Curr Allergy

Asthma Rep. 2004 Jul;4(4):270-5. PMID: 15175140

" The increased prevalence of atopic diseases, atopic dermatitis,

allergic rhinitis, and asthma has been described as an epidemic. New

approaches in the fight against allergic diseases are called for,

the target being the persistence of the atopic T helper 2-skewed

immune responder pattern beyond infancy. Atopic dermatitis, the

earliest of these conditions, might act as a portal for the

development of IgE-mediated atopic manifestations. Abundant evidence

implies that specific strains selected from the healthy gut

microbiota exhibit powerful antipathogenic and anti-inflammatory

capabilities, and several targets for the probiotic approach have

emerged in atopic dermatitis: degradation/structural modification of

enteral antigens, normalization of the properties of aberrant

indigenous microbiota and of gut barrier functions, regulation of

the secretion of inflammatory mediators, and promotion of the

development of the immune system. Better understanding of the

effects of different probiotic strains and deeper insight into the

mechanisms of the heterogeneous manifestations of atopic disease are

needed for the validation of specific strains carrying anti-allergic

potential. "

212. Cross ML. Immune-signalling by orally-delivered probiotic

bacteria: effects on common mucosal immunoresponses and protection

at distal mucosal sites. Int J Immunopathol Pharmacol. 2004 May-

Aug;17(2):127-34. PMID: 15171813

" Probiotics--orally-delivered preparations of non-pathogenic

bacterial cells--have been reported to increase anti-microbial

protection in the gastrointestinal tract environment, and offer a

safe and effective non-pharmaceutical means for combating infectious

diseases and certain other pathologies. There is also an increasing

body of evidence to suggest that immunostimulation by probiotic

bacteria in the gut can enhance immune protection at distal mucosal

sites, such as the urogenital and respiratory tracts. This review

summarises the current information, from both clinical and animal

model studies, of a role for orally-delivered probiotics in

modulating mucosal immunoresponses and protection at distal sites.

While it is clear that probiotics hold promise in this area,

research that is targeted toward identifying the mechanism driving

stimulation of the common mucosal immune system, as well as patterns

of mucosal tissue homing by immunocytes following probiotic-mediated

signalling in the gut, is strongly encouraged. "

213. Drakes M et al. Bacterial probiotic modulation of dendritic

cells. Infect Immun. 2004 Jun;72(6):3299-309 PMID: 15155633

" Intestinal dendritic cells are continually exposed to ingested

microorganisms and high concentrations of endogenous bacterial

flora. These cells can be activated by infectious agents and other

stimuli to induce T-cell responses and to produce chemokines which

recruit other cells to the local environment. Bacterial probiotics

are of increasing use against intestinal disorders such as

inflammatory bowel disease. They act as nonpathogenic stimuli within

the gut to regain immunologic quiescence. This study was designed to

determine the ability of a bacterial probiotic cocktail VSL#3 to

alter cell surface antigen expression and cytokine production in

bone marrow-derived dendritic cell-enriched populations. Cell

surface phenotype was monitored by monoclonal fluorescent antibody

staining, and cytokine levels were quantitated by enzyme-linked

immunosorbent assay. High-dose probiotic upregulated the expression

of C80, CD86, CD40, and major histocompatibility complex class II I-

Ad. Neither B7-DC or B7RP-1 was augmented after low-dose probiotic

or Lactobacillus casei treatment, but B7RP-1 showed increased

expression on dendritic cells stimulated with the gram-negative

bacterium Escherichia coli. Functional studies showed that probiotic

did not enhance the ability of dendritic cells to induce allogeneic

T-cell proliferation, as was observed for E. coli. Substantial

enhancement of interleukin-10 release was observed in dendritic cell-

enriched culture supernatants after 3 days of probiotic stimulation.

These results demonstrate that probiotics possess the ability to

modulate dendritic cell surface phenotype and cytokine release in

granulocyte-macrophage colony-stimulating factor-stimulated bone

marrow-derived dendritic cells. Regulation of dendritic cell

cytokines by probiotics may contribute to the benefit of these

molecules in treatment of intestinal diseases. "

Immune impairments in autism

214. Warren RP et al. Brief report: immunoglobulin A deficiency in a

subset of autistic subjects. J Autism Dev Disord. 1997 Apr;27(2):187-

92. PMID: 9105969

215. Strong association of the third hypervariable region of HLA-DR

beta 1 with autism. J Neuroimmunol. 1996 Jul;67(2):97-102. PMID:

8765331

216. Immunogenetic studies in autism and related disorders.Mol Chem

Neuropathol. 1996 May-Aug;28(1-3):77-81. PMID: 8871944

217. Elevated serotonin levels in autism: association with the major

histocompatibility complex. Neuropsychobiology. 1996;34(2):72-5.

PMID: 8904735

218. Increased frequency of the extended or ancestral haplotype B44-

SC30-DR4 in autism. Neuropsychobiology. 1995;32(3):120-3. PMID:

8544967

219. DR-positive T cells in autism: association with decreased

plasma levels of the complement C4B protein. Neuropsychobiology.

1995;31(2):53-7. PMID: 7760985

220. Decreased plasma concentrations of the C4B complement protein

in autism. Arch Pediatr Adolesc Med. 1994 Feb;148(2):180-3. PMID:

8118537

221. Increased frequency of the null allele at the complement C4b

locus in autism. Clin Exp Immunol. 1991 Mar;83(3):438-40. PMID:

2004485

222. Reduced natural killer cell activity in autism. J Am Acad Child

Adolesc Psychiatry. 1987 May;26(3):333-5. PMID: 3597287

223. Immune abnormalities in patients with autism. J Autism Dev

Disord. 1986 Jun;16(2):189-97. PMID: 2941410

Methylcobalamin miscellany

225. Intestinal absorption and concurrent chemical changes of

methylcobalamin. J Lab Clin Med. 1973 Apr;81(4):557-67. PMID:

4696188

226. Detection of malabsorption of vitamin B12 due to gastric or

intestinal dysfunction. Semin Nucl Med. 1972 Jul;2(3):220-34. PMID:

4625601

227. Vitamin B 12 malabsorption in chronic pancreatic insufficiency.

N Engl J Med 1971 Mar 25;284(12):627-32. PMID: 5547614

228. Complex of intrinsic factor and B12 in human ileum during

vitamin B12 absorption. Am J Physiol. 1968 Apr;214(4):832-5. PMID:

5642944

229. The binding of methylcobalamin and vitamin-B 12 coenzyme. S Afr

Med J. 1970 May 2;44(18):537-9. PMID: 5445924

230. Competition between bacteria and intrinsic factor for vitamin B

12: implications for vitamin B 12 malabsorption in intestinal

bacterial overgrowth. Gastroenterology. 1972 Feb;62(2):255-60.

PMID: 4629318

231. Effect of small intestinal bacteria on intrinsic factor and the

vitamin B 12-intrinsic factor complex. Scand J Gastroenterol.

1971;6(8):707-13.

232. Correction of cobalamin malabsorption in pancreatic

insufficiency with a cobalamin analogue that binds with high

affinity to R protein but not to intrinsic factor. In vivo evidence

that a failure to partially degrade R protein is responsible for

cobalamin malabsorption in pancreatic insufficiency. J Clin Invest.

1978 Jun;61(6):1628-34. PMID: 659618

233. Absorption studies in patients with Crohn's disease and in

patients with ulcerative colitis. Acta Med Scand. 1971 Nov;190

(5):407-10. PMID: 5149268

234. Production of vitamin B 12 analogues in patients with small-

bowel bacterial overgrowth. Ann Intern Med. 1977 Nov;87(5):546-51.

PMID: 921081

Thus bacterial production of cobamides, both de novo and from

ingested CN-Cbl

bound to intrinsic factor, occurs in humans with bacterial

overgrowth states and results in a significant loss of vitamin B12

to the host. "

[b12 lab result may indicate extreme high, a false positive in some

cases]

235. Current concepts of cobalamin (vitamin B12) absorption and

malabsorption. J Clin Gastroenterol. 1980 Sep;2(3):287-97. PMID:

7005313

236. The effect of intrinsic factor proteins on the methylating

activity of CH3-B12 coenzyme. Bull Acad Pol Sci Biol. 1975;23

(6):361-4. PMID: 1164687

237. Neubrander, M.D. -- Biochemical Context and Clinical Use

of Methyl B12 DAN! 2003 Philadelphia

http://64.202.182.52/powerpoint/dan2003/Neubrander.htm

238. Neubrander, M.D. -- Case presentation of Children with

Autism Spectrum Disorder DAN! 2003 Philadelphia

http://64.202.182.52/powerpoint/dan2003/Neubrander.htm

239. Neubrander, M.D. -- Biochemical Context And Clinical Use

Of Vitamin B12. DAN! 2004, Washington, D.C.

240. Walsh WJ et al. Reduced violent behavior following biochemical

therapy. Physiol Behav. 2004 Oct 15;82(5):835-9. Pfeiffer Treatment

CenterWarrenville, IL 60555 PMID: 15451647

" Reduced violent behavior following biochemical therapy. We

conducted an outcome study to measure the effectiveness of

biochemical therapy for 207 consecutive patients presenting with a

diagnosed behavior disorder. The treatment protocols were based on

clinical evaluation and our past experience in the treatment of 8000

patients with behavior disorders at the Pfeiffer Treatment Center

(PTC) over a 10-year period. Each test subject was screened for

chemical imbalances previously found in high incidence in this

population, including metal-metabolism disorders, methylation

abnormalities, disordered pyrrole chemistry, heavy-metal overload,

glucose dyscontrol, and malabsorption. The clinical procedure

included a medical history, assay of 90 biochemical factors, and a

physical examination. Standardized treatment protocols were applied

for each imbalance that was identified. The frequencies of physical

assaults and destructive episodes were determined using a

standardized behavior scale before and after treatment, with follow-

up ranging from 4 to 8 months. RESULTS: Seventy-six percent of the

test subjects achieved compliance during the treatment period. The

remaining 24% were reported to have discontinued the therapy. A

reduced frequency of assaults was reported by 92% of the compliant

assaultive patients, with 58% achieving elimination of the behavior.

A total of 88% of compliant destructive patients exhibited a reduced

frequency of destructive incidents and 53% achieved elimination of

the behavior. Statistical significance was found for reduced

frequency of assaults (t=7.74, p<0.001) and destructive incidents

(t= 8.77, p<0.001). The results of this outcome study strongly

suggest that individualized biochemical therapy may be efficacious

in achieving behavioral improvements in this patient population.

Epileptiform pattern in autism

241: Nasr JT et al. The Electroencephalogram in Children with

Developmental Dysphasia. Epilepsy Behav. 2001 Apr;2(2):115-118.

PMID: 12609193

Speech and language delay is a common developmental or acquired

disorder. It can be a feature of the autistic spectrum, and if

regression of language coincides with epilepsy, the diagnosis of

Landau-Kleffner syndrome is considered. Slow acquisition of language

without regression is called developmental dysphasia. A

retrospective review of clinical and electroencephalographic

(including video electroencephalographic) data on 138 children with

speech/language delay, seen in a year's time, is presented. The

electroencephalogram (EEG) was abnormal in 61% of children with a

history of language regression. The EEG was abnormal in

only 15% of children with developmental language disorder, most of

whom also had clinical seizures. The difference between the two

groups was highly significant (P = 0.004). Therefore obtaining an

EEG in children with regression of language, especially if a history

of clinical seizures is elicited, is indicated.

242. Wheless JW et al. Language dysfunction in epileptic

conditions. Semin Pediatr Neurol. 2002 Sep;9(3):218-28. PMID:

12350043

Epilepsy may disrupt brain functions necessary for language

development by its associated intellectual disabilities or directly

as a consequence of the seizure disorder. Additionally, in recent

years, there has been increasing recognition of the association of

epileptiform electroencephalogram (EEG) abnormalities with language

disorders and autism spectrum disorders. Any process that impairs

language function has long-term consequences for academic, social,

and occupational adjustments in children and adolescents with

epilepsy. Furthermore, impairments in specific language abilities

can impact memory and learning abilities. This article reviews

interictal language function in children and adults with epilepsy;

epilepsy surgery and language outcome; and language disorders

associated with abnormal EEGs. The relationship between epilepsy and

language function is complicated as the neuroanatomic circuits

common to both overlap. We demonstrate how magnetoencephalography

(MEG) offers the ability to analyze the relationship of language,

EEG abnormalities, and epilepsy.

243. Hrdlicka M et al. Not EEG abnormalities but epilepsy is

associated with autistic regression and mental functioning in

childhood autism. Eur Child Adolesc Psychiatry. 2004 13(4):209-13.

The aim of the study was to investigate the potential association of

epilepsy and EEG abnormalities with autistic regression and mental

retardation. We examined a group of 77 autistic children (61 boys,

16 girls) with an average age of 9.1 +/- 5.3 years. Clinical

interview, neurological examination focused on the evaluation of

epilepsy, IQ testing, and 21-channel EEG (including night sleep EEG

recording) were performed. Normal EEGs were observed in 44.4% of the

patients, non-epileptiform abnormal EEGs in 17.5%, and abnormal EEGs

with epileptiform discharges in 38.1% of the patients. Epilepsy was

found in 22.1% of the subjects. A history of regression was reported

in 25.8% of the patients, 54.8% of the sample had abnormal

development during the first year of life, and 79.7% of the patients

were mentally retarded. Autistic regression was significantly more

frequent in patients with epilepsy than in non-epileptic patients (p

= 0.003). Abnormal development during the first year of life was

significantly associated with epileptiform EEG abnormalities (p =

0.014). Epilepsy correlated significantly with mental retardation (p

= 0.001). Although the biological basis and possible causal

relationships of these associations remain to be explained, they may

point to different subgroups of patients with autistic spectrum

disorders.

244. McVicar KA, Shinnar S. Landau-Kleffner syndrome, electrical

status epilepticus in slow wave sleep, and language regression in

children. Ment Retard Dev Disabil Res Rev. 2004;10(2):144-9. PMID:

15362173

The Landau-Kleffner syndrome (LKS) and electrical status epilepticus

in slow wave sleep (ESES) are rare childhood-onset epileptic

encephalopathies in which loss of language skills occurs in the

context of an epileptiform EEG activated in sleep. Although in LKS

the loss of function is limited to language, in ESES there is a

wider spectrum of cognitive impairment. The two syndromes are

distinct but have some overlap. The relationship between the

epileptiform EEG abnormalities and the loss of cognitive function

remains controversial, even in LKS which is the most widely accepted

as an acquired epileptic aphasia. Language regression also occurs in

younger children, frequently in the context of a more global

autistic regression. Many of these children have epileptiform EEGs.

The term autistic regression with epileptiform EEG has been proposed

for these children. Whether these children are part of an extended

LKS spectrum is very controversial, because there are differences in

age of onset, clinical phenotype, and EEG findings. An understanding

of the available data on clinical characteristics, EEG findings,

pathology, prognosis, and treatment of these syndromes is essential

for further progress in this area.

245. Tharp BR. Epileptic encephalopathies and their relationship to

developmental disorders: Do spikes cause autism? Ment Retard Dev

Disabil Res Rev. 2004;10(2):132-4.

Epileptic encephalopathies are progressive clinical and

electroencephalographic syndromes where deterioration is thought to

be caused by frequent seizures and abundant EEG epileptiform

activity. Seizures occur in approximately 10-15% of children with

pervasive developmental disorders (PDD) and 8-10% have epileptiform

EEG abnormalities without seizures. Thirty percent of children with

PDD have regression of social behavior and language at 2-3 years of

age. Some authors speculate that the regression is caused by

epileptiform activity even in the absence of overt clinical seizures

( " autism with epileptic regression " ) and suggest that elimination of

the epileptiform activity, either medically or surgically, should

lead to improvement in behavior. This review examines the data

showing that interictal epileptiform discharges are associated with

transient clinical dysfunction and discusses the implications of

these observations for autistic behavioral abnormalities. The

results of resective surgery, vagal nerve stimulation, and multiple

subpial transaction on children with autism and epileptiform EEG

abnormalities are also discussed. I conclude that there is no

evidence that interictal discharges per se cause (or contribute to)

the complex behavioral phenotype of autism. There is no

justification to support the use of anticonvulsant medication or

surgery in children with PDD

without seizures; that is, there is no evidence that treatment to

eliminate EEG spikes will have a therapeutic effect on the

behavioral abnormalities of PDD and autism.

246. Chez MG et al. Frequency of EEG abnormalities in age-matched

siblings of autistic children with abnormal sleep EEG patterns.

Epilepsy Behav. 2004 Apr;5(2):159-62. PMID: 15123015

Epileptiform activity in sleep has been described even in the

absence of clinical seizures in 43-68% of patients with autistic

spectrum disorders (ASDs). Genetic factors may play a significant

role in the frequency of epilepsy, yet the frequency in normal age-

matched controls is unknown. We studied overnight ambulatory

electroencephalograms (EEGs) in 12 nonepileptic, nonautistic

children with a sibling with both ASDs and an abnormal EEG. EEG

studies were read and described independently by two pediatric

epileptologists; 10 were normal studies and 2 were abnormal. The

occurrence of abnormal EEGs in our sample (16.6%) was lower than the

reported occurrence in children with ASDs. Further, the two abnormal

EEGs were of types typically found in childhood and were different

from those found in the ASD-affected siblings. The lack of

similarity between sibling EEGs suggests that genetic factors alone

do not explain the higher frequency of EEG abnormalities reported in

ASDs.

Amino acids & epileptiform activity

247. Park YD. The effects of vagus nerve stimulation therapy on

patients with intractable

seizures and either Landau-Kleffner syndrome or autism. Epilepsy

Behav. 2003 Jun;4(3):286-90. PMID: 12791330

Acquired and developmental comorbid conditions, including language

and behavioral disorders, are often associated with epilepsy.

Although the relationship between these disorders is not fully

understood, their close association may indicate that they share

common features, suggesting that these conditions may respond to the

same therapies. Not only has vagus nerve stimulation (VNS) therapy

been proven to reduce the frequency of pharmacoresistant seizures in

epilepsy patients, but preliminary studies also indicate that VNS

therapy may improve neurocognitive performance. On the basis of

these findings, we hypothesized that VNS therapy would improve the

quality of life of patients with either Landau-Kleffner syndrome

(LKS) or autism, independent of its effects on seizures. Data were

retrospectively queried from the VNS therapy patient outcome

registry (Cyberonics, Inc; Houston, TX, USA). A constant cohort of 6

LKS patients and 59 autistic patients were identified. Among the LKS

patients, 3 patients at 6 months experienced at least a 50%

reduction in seizure frequency as compared with baseline. Physicians

reported quality-of-life improvements in all areas assessed for at

least 3 of the 6 children. More than half of the patients with

autism (58%) experienced at least a 50% reduction in seizure

frequency at 12 months. Improvements in all areas of quality of life

monitored were reported for most patients, particularly for

alertness (76% at 12 months). Although these preliminary findings

are encouraging, a prospective study using standardized measurement

tools specific to these disorders and a longer-term follow-up are

necessary to better gauge the efficacy of VNS therapy among these

patient populations.

248. El Idrissi A et al. Prevention of epileptic seizures by

taurine. Adv Exp Med Biol. 2003;526:515-25. PMID: 12908638

249. Dufour F et al. Modulation of absence seizures by branched-

chain amino acids: correlation with brain amino acid concentrations.

Neurosci Res. 2001 Jul;40(3):255-63. PMID: 11448517

250. Borowicz KK et al. Two essential amino acids, L-lysine and L-

histidine, in five types of experimental seizures. Pol J Pharmacol.

2000 Sep-Oct;52(5):345-52. PMID: 11334226

L-Lysine (250-2,000 mg/kg) and L-histidine (1,000-2,000 mg/kg)

significantly raised the electroconvulsive threshold. D-Histidine

(1,000 mg/kg) was completely ineffective in this regard. Both amino

acids were generally inactive in pentetrazole-, picrotoxin- and

aminophylline-induced seizures, though L-histidine (2,500 mg/kg)

significantly reduced the number of mice with clonic convulsions in

the pentetrazole test. Also, L-lysine (2,500 and 3,000 mg/kg)

significantly diminished mortality rate in aminophylline-induced

seizures. In addition, L-lysine (2,500-3,000 mg/kg) and L-histidine

(2,000-2,500 mg/kg) delayed the onset of aminophylline- and

picrotoxin-evoked convulsions. L-Lysine and L-histidine (both up to

1,000 mg/kg) did not affect amygdala-kindled seizures in rats. The

results indicate that some of indispensable amino acids may play a

role in the inhibitory transmission in the central nervous system. A

possibility arises that appropriate diet may be an important

supportive factor in the treatment of some epileptic patients,

probably suffering from generalized tonic-clonic seizures.

251. Kirchner A et al. Effects of taurine and glycine on

epileptiform activity induced by removal of Mg2+ in combined rat

entorhinal cortex-hippocampal slices. Epilepsia. 2003 Sep;44(9):1145-

52. PMID: 12919385

PURPOSE: The imbalance between neuronal inhibition and excitation

contributes to epileptogenesis. Inhibition in the central nervous

system (CNS) is mediated by gamma-aminobutyric acid (GABA) and

glycine. Recent studies indicate the expression of glycine receptor

(GlyR) in hippocampus and neocortex. However, the function of GlyR

in these regions is not clarified completely. The aim of this study

was to investigate whether the GlyR agonists glycine and taurine

promote an anticonvulsive effect…. Likewise glycine, after an

initial proconvulsant effect, suppressed epileptiform discharges.

CONCLUSIONS: These findings show that GlyR agonists, in particular

taurine, could serve as potential anticonvulsants and suggest an

important role of GlyR in cortical function and dysfunction.

252. Gietzen DW et al. Indispensable amino acid deficiency and

increased seizure susceptibility in rats. Am J Physiol. 1996 Jul;271

(1 Pt 2):R18-24. PMID: 8760199

Repeated subthreshold stimulation of limbic brain areas increases

seizure susceptibility in experimental models of epilepsy. In

addition, acute dietary indispensable amino acid (IAA) deficiency

activates the anterior piriform cortex (APC), a seizure-prone limbic

brain area in the rat. Based on these two findings, we hypothesized

that activation of the APC by chronic exposure to IAA-deficient

diets might increase seizure susceptibility. Several nonessential

amino acid neurotransmitters are important in seizures, but

deficiencies of nontransmitter IAAs have not been well studied in

seizure models. In four trials, we made injections of

pentylenetetrazole intraperitoneally or of bicuculline into the APC

in histidine-, isoleucine-, or threonine-deficient rats and

controls. Increased susceptibility to seizures in the deficient

animals was observed as increased severity of the seizures,

decreased threshold for the dose of the chemostimulant and time to

seizure, or a combination thereof. Pair-fed controls showed that

this effect was not due to an energy deficit. This novel but robust

finding suggests that IAA deficiency may increase vulnerability to

seizures by repeated activation of the APC.

253. Hammen A et al. A paradoxical rise of neonatal seizures after

treatment with vitamin B6. Eur J Paediatr Neurol. 1998;2(6):319-22.

PMID: 10727199

We report the case of a newborn with intractable epileptic seizures

developing a paradoxical rise of seizure frequency and

electroencephalogram alterations after administration of vitamin B6.

We have been unable to determine the aetiology of this disorder. In

a newborn presenting with drug-resistant epileptic seizures, the

first therapeutic option remains the application of intravenous

pyridoxine, but the physician should be aware of the risk of an

increase in seizure frequency.

Autism Treatment Evaluation Checklist (ATEC)

254. Autism Treatment Evaluation Checklist (ATEC)

Internet Scoring Program

http://www.autismeval.com/ari-atec/index.html

New Autism Epidemiology Study

whole article free online

http://www.publichealthreports.org/article/PIIS0033354904001347/abstr

act

http://download.journals.elsevierhealth.com/pdfs/journals/0033-

3549/PIIS0033354904001347.pdf

255. Blaxil MF. What's going on? The question of time trends in

autism. Public Health Reports 119.6. 536-551 (November 2004)

Synopsis: Increases in the reported prevalence of autism and

autistic spectrum disorders in recent years have fueled concern over

possible environmental causes. The author reviews the available

survey literature and finds evidence of large increases in

prevalence in both the United States and the United Kingdom that

cannot be explained by changes in diagnostic criteria or

improvements in case ascertainment. Incomplete ascertainment of

autism cases in young child populations is the largest source of

predictable bias in prevalence surveys; however, this bias has, if

anything, worked against the detection of an upward trend in recent

surveys. Comparison of autism rates by year of birth for specific

geographies provides the strongest basis for trend assessment. Such

comparisons show large recent increases in rates of autism and

autistic spectrum disorders in both the U.S. and the U.K. Reported

rates of autism in the United States increased from ,3 per 10,000

children in the 1970s to .30 per 10,000 children in the 1990s, a 10-

fold increase. In the United Kingdom, autism rates rose from ,10 per

10,000 in the 1980s to roughly 30 per 10,000 in the 1990s. Reported

rates for the full spectrum of autistic disorders rose from the 5 to

10 per 10,000 range to the 50 to 80 per 10,000 range in the two

countries. A precautionary approach suggests that the rising

incidence of autism should be a matter of urgent public concern.

Link to comment
Share on other sites

Guest guest

http://www.autismwebsite.com/ari/vaccine/thimerosalreferences.htm

The Vaccine-Autism Connection – Part I (Thimerosal)

Read and download an Adobe Acrobat (pdf) file

BERNARD RIMLAND, Ph.D., Director

April, 2004

Partial list of studies linking thimerosal to Autism

The Centers for Disease Control and the American Academy of

Pediatrics have issued a statement asserting that " the available

scientific evidence has not shown thimerosal-containing vaccines to

be harmful. " Their statement is false. Following are some of the

scientific studies that demonstrate thimerosal, a mercury-containing

substance that is used as a preservative, to be harmful and to be a

highly probably causal factor in autism. Note that these studies

are consistently ignored in the medical establishment's publications

claiming that there is no evidence for vaccine-caused autism.

Bernard S, Enayati A, Redwood L, H, Binstock T. Autism: a

novel form of mercury poisoning. Med. Hypotheses. 2001 Apr;56(4):462-

71. PMID: 11339848

Geier DA, Geier MR. An assessment of the impact of thimerosal on

childhood neurodevelopmental disorders. Pediatr Rehabil. 2003 Apr-

Jun;6(2):97-102. PMID: 14534046

Geier MR, Geier DA. Neurodevelopmental disorders after thimerosal-

containing vaccines: a brief communication. Exp Biol Med (Maywood).

2003 Jun;228(6):660-4. PMID: 12773696

Geier & Geier. Parents' worries about thimerosal in vaccines are

well founded!

http://pediatrics.aappublications.org/cgi/eletters/112/6/1394

Baskin, M.D. et al. Thimerosal induces DNA breaks, caspase-3

activation, membrane damage, and cell death in cultured human

neurons and fibroblasts. Toxicol Sci. 2003 Aug;74(2):361-8. Epub

2003 May 28. PMID: 12773768

Mady Hornig, M.D Etiologic factors and pathogenesis of autism:

evidence from clinical studies and animal models. IOM presentation,

Feb 9 2004 Audio only: http://www.iom.edu/view.asp?id=19108

C. Deth, Ph.D. Effects of Mercury on Methionine Synthase:

Implications for Disordered Methylation in Autism DAN! 2003

Philadelphia -

http://64.202.182.52/powerpoint/dan2003/Deth.htm

C. Deth, Ph.D. A Link Between Thimerosal and the Brain:

Can Vaccines Affect Central Nervous System Function? Molecular

Psychiatry 2004, Volume 9.

Vojdani A, Pangborn JB et al. Infections, toxic chemicals and

dietary peptides binding to lymphocyte receptors and tissue enzymes

are major instigators of autoimmunity in autism. Int J Immunopathol

Pharmacol. 2003 Sep-Dec;16(3):189-99. PMID: 14611720

Jeff Bradstreet, M.D. A Case-control Study of Mercury Burden in

Children with Autistic Disorders and Measles Virus Genomic RNA in

Cerebrospinal Fluid in Children with Regressive Autism. IOM

presentation, Feb 9, 2004

Slides: http://www.iom.edu/view.asp?id=18578

Audio: http://www.iom.edu/view.asp?id=19130

Valsamakis A et al. style='mso-bidi-font-style:italic'>Altered

virulence of vaccine strains of measles virus after prolonged

style='mso-bidi-font-style: italic'>replication in human tissue. J

Virol. 1999 73(10): 8791-7. PMID 10482633

http://jvi.asm.org/cgi/reprint/73/10/8791.pdf

The CDC's original findings before the CDC began to manipulate the

data, obtained via the Freedom of Information Act: High risk values

for thimerosal injections and a range of neurologic problems,

including ADHD, tics, language problems, and autism.

http://factsformedia.com/factsformedia/thimerosalstudy.pdf

Excerpts from CDC's in-house conference: Thimerosal sequelae

http://www.nationalautismassociation.org/library/IOM%20Simpsonwood%

20in%20bold.pdf

Congressman, Dr. Weldon's letter to the CDC director, available at:

http://momsonamissionforautism.org/Autism_Central/Dr_Weldon_Responds.

shtml

Institute of Medicine presentation of Congressman Dave Weldon, M.D.

http://www.nationalautismassociation.org/pdf/Weldon.pdf

Geier MR, Geier DA. Autism and thimerosal-containing vaccines:

analysis of the Vaccine Adverse Events Reporting System (VAERS). IOM

presentation, Feb 9, 2004.

Slides: http://www.iom.edu/view.asp?id=18392

Audio: http://www.iom.edu/view.asp?id=19120

Baskin, M.D. Relation of Neurotoxic Effects of Thimerosal to

Autism. IOM presentation, Feb 9, 2004.

Audio only: http://www.iom.edu/view.asp?id=19124

Link to comment
Share on other sites

Guest guest

Several reasons you should know about for the lack of controlled studies...

1. Parents who have learned about mercury toxicity wouldn't want to take a

chance that their child would get a placebo, particularly when dosing every 3

hours day and night!

2. Controlled studies require limiting the variables. Most who chelate do many

different interventions if they appear to help and wouldn't want to do only

chelation if other things can help.

3. Much research is paid for by pharmaceutical companies. Pharmaceutical

companies make much of what causes mercury toxicity so even if they did the

research it's unlikely that it would provide accurate info for consumers. They

tend to fund research that will bring more money their way. They make many of

the drugs which people with mercury poisoning take to try to control symptoms.

If people find out that over-the-counter chelators work they lose business.

S S

<BR>

In a message dated 09/05/2006 17:46:57 GMT Daylight Time, zyan@...  <BR>

writes:<BR>

<BR>

I'm new  to the group and just wondered if anyone could point me to any <BR>

research  that shows that chelation works in removing the mercury from <BR>

the brain and  body, have there been any controlled studies.  I am not <BR>

a parent just  an interested professional who works with asd kids, and <BR>

admittedly am  shocked by all of this.  I am also considering this as a <BR>

treatment  for myself due to mercury exposure from amalgam  fillings.<BR>

_______________________________________________

Join Excite! - http://www.excite.com

The most personalized portal on the Web!

Link to comment
Share on other sites

Guest guest

There are some books on chelation following amalgam removal. They

show patients symptoms disappearing, and blood work normalizing. You

may want to read a book called " It's All in Your Head " by Hal

Huggins. He did a lot of research on treating people for mercury

toxicity. He also enlisted the help of some scientist to prove that

this stuff does things to you. Sorry to be so untechnical. I did

read the book twice, I am just not good at descriptions. But if you

really dig..there are studies on chelation of mercury and other

toxins in general. Just not specific to ASD kids.

>

>

> Several reasons you should know about for the lack of controlled

studies...

> 1. Parents who have learned about mercury toxicity wouldn't want

to take a chance that their child would get a placebo, particularly

when dosing every 3 hours day and night!

> 2. Controlled studies require limiting the variables. Most who

chelate do many different interventions if they appear to help and

wouldn't want to do only chelation if other things can help.

> 3. Much research is paid for by pharmaceutical companies.

Pharmaceutical companies make much of what causes mercury toxicity

so even if they did the research it's unlikely that it would provide

accurate info for consumers. They tend to fund research that will

bring more money their way. They make many of the drugs which

people with mercury poisoning take to try to control symptoms. If

people find out that over-the-counter chelators work they lose

business.

> S S

>

>

> <BR>

> In a message dated 09/05/2006 17:46:57 GMT Daylight Time,

zyan@...  <BR>

> writes:<BR>

> <BR>

> I'm new  to the group and just wondered if anyone could point me

to any <BR>

> research  that shows that chelation works in removing the mercury

from <BR>

> the brain and  body, have there been any controlled studies.  I am

not <BR>

> a parent just  an interested professional who works with asd kids,

and <BR>

> admittedly am  shocked by all of this.  I am also considering this

as a <BR>

> treatment  for myself due to mercury exposure from amalgam 

fillings.<BR>

>

>

> _______________________________________________

> Join Excite! - http://www.excite.com

> The most personalized portal on the Web!

>

Link to comment
Share on other sites

Guest guest

Iowa DAMS also put out a book about adults who have recovered or are recovering

from mercury poisoning from their dental fillings.

Hal Huggins, by the way, was a dentist who was diagnosed with MS until he dealt

with his own mercury toxicity.

S S

There are some books on chelation following amalgam removal. They <BR>

show patients symptoms disappearing, and blood work normalizing. You <BR>

may want to read a book called " It's All in Your Head " by Hal <BR>

Huggins. He did a lot of research on treating people for mercury <BR>

toxicity.  He also enlisted the help of some scientist to prove that <BR>

this stuff does things to you. Sorry to be so untechnical. I did <BR>

read the book twice, I am just not good at descriptions. But if you <BR>

really dig..there are studies on chelation of mercury and other <BR>

toxins in general. Just not specific to ASD kids.<BR>

<BR>

_______________________________________________

Join Excite! - http://www.excite.com

The most personalized portal on the Web!

Link to comment
Share on other sites

Guest guest

My symptoms are getting better as I lose my amalgams. However I didn't follow

good procedure, didn't know better, so some symptoms are better, some are worse.

I now can get diagnosed with ADD in about 30 seconds by any professional as my

symptoms are that pronounced. I have one more amalgam and one crown that has to

be checked out and I am going to start chelation, Andy's protocol of course!!

I think amalgams are a good part of what is making people sick. Our bodies

are so consumed with detoxing everything we take in it can't fight off real

illnesses. Cancer is now what kills the majority of people in this country and

that is certainly not something caught by touching a dirty doorknob. Little

illnesses are our bodies " check engine " light. We need to take care of that and

cure it not mask it with drugs. That is like unplugging that light in your car

vs. going to a shop and fixing the problem. Do that and eventually the car will

just die. Our bodies aren't that different.

Another 2 cents of mine!

Jan <queenvavee@...> wrote:

There are some books on chelation following amalgam removal. They

show patients symptoms disappearing, and blood work normalizing. You

may want to read a book called " It's All in Your Head " by Hal

Huggins. He did a lot of research on treating people for mercury

toxicity. He also enlisted the help of some scientist to prove that

this stuff does things to you. Sorry to be so untechnical. I did

read the book twice, I am just not good at descriptions. But if you

really dig..there are studies on chelation of mercury and other

toxins in general. Just not specific to ASD kids.

>

>

> Several reasons you should know about for the lack of controlled

studies...

> 1. Parents who have learned about mercury toxicity wouldn't want

to take a chance that their child would get a placebo, particularly

when dosing every 3 hours day and night!

> 2. Controlled studies require limiting the variables. Most who

chelate do many different interventions if they appear to help and

wouldn't want to do only chelation if other things can help.

> 3. Much research is paid for by pharmaceutical companies.

Pharmaceutical companies make much of what causes mercury toxicity

so even if they did the research it's unlikely that it would provide

accurate info for consumers. They tend to fund research that will

bring more money their way. They make many of the drugs which

people with mercury poisoning take to try to control symptoms. If

people find out that over-the-counter chelators work they lose

business.

> S S

>

>

> <BR>

> In a message dated 09/05/2006 17:46:57 GMT Daylight Time,

zyan@... <BR>

> writes:<BR>

> <BR>

> I'm new to the group and just wondered if anyone could point me

to any <BR>

> research that shows that chelation works in removing the mercury

from <BR>

> the brain and body, have there been any controlled studies. I am

not <BR>

> a parent just an interested professional who works with asd kids,

and <BR>

> admittedly am shocked by all of this. I am also considering this

as a <BR>

> treatment for myself due to mercury exposure from amalgam

fillings.<BR>

>

>

> _______________________________________________

> Join Excite! - http://www.excite.com

> The most personalized portal on the Web!

>

=======================================================

Link to comment
Share on other sites

Guest guest

>

> Hi

> I'm new to the group and just wondered if anyone could point me to any

> research that shows that chelation works in removing the mercury from

> the brain and body, have there been any controlled studies.

I can tell you that " on's Principles of Internal Medicine " , a

standard med school text, says that chelation is the treatment for

heavy metal poisoning. Most doctors have no experience with it and so

are scared of it, but it is the recommendation in their textbooks.

I am not

> a parent just an interested professional who works with asd kids, and

> admittedly am shocked by all of this.

It is shocking! If you keep reading here, you'll see lots of posts

from people whose children are getting better thanks to chelation

using the Andy Cutler protocol described in the files of the list.

Unfortunately the broken trust in mainstream medicine has led many of

us to put at least as much weight on the anecdotal experiences related

here, since we've seen how easily controlled studies can be corrupted

and suffered the damage caused by following medical advice.

> I am also considering this as a

> treatment for myself due to mercury exposure from amalgam fillings.

Andy's books, " Amalgam Illness " and " Hair Test Interpretation " , would

be very very helpful for you. Good luck.

Nell

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...