Guest guest Posted January 5, 2006 Report Share Posted January 5, 2006 Hi, shakerz25. The connection between apolipoprotein E4 genotype and problems with mercury detox was new to me, but I did find the following abstracts on PubMed: " J Alzheimers Dis. 2003 Jun;5(3):189-95. Apolipoprotein E genotyping as a potential biomarker for mercury neurotoxicity. Godfrey ME, Wojcik DP, Krone CA. Bay of Plenty Environmental Health Clinic, Tauranga, New Zealand. godfrey@... Apolipoprotein-E (apo-E) genotyping has been investigated as an indicator of susceptibility to heavy metal (i.e., lead) neurotoxicity. Moreover, the apo-E epsilon (epsilon)4 allele is a major risk factor for neurodegenerative conditions, including Alzheimer's disease (AD). A theoretical biochemical basis for this risk factor is discussed herein, supported by data from 400 patients with presumptive mercury-related neuro-psychiatric symptoms and in whom apo-E determinations were made. A statistically relevant shift toward the at-risk apo-E epsilon4 groups was found in the patients p<0.001). The patients possessed a mean of 13.7 dental amalgam fillings and 31.5 amalgam surfaces. This far exceeds the number capable of producing the maximum identified tolerable daily intake of mercury from amalgam. The clinical diagnosis and proof of chronic low-level mercury toxicity has been difficult due to the non- specific nature of the symptoms and signs. Dental amalgam is the greatest source of mercury in the general population and brain, blood and urine mercury levels increase correspondingly with the number of amalgams and amalgam surfaces in the mouth. Confirmation of an elevated body burden of mercury can be made by measuring urinary mercury, after provocation with 2,3,-dimercapto-propane sulfonate (DMPS) and this was measured in 150 patients. Apo-E genotyping warrants investigation as a clinically useful biomarker for those at increased risk of neuropathology, including AD, when subjected to long-term mercury exposures. Additionally, when clinical findings suggest adverse effects of chronic mercury exposure, a DMPS urine mercury challenge appears to be a simple, inexpensive procedure that provides objective confirmatory evidence. An opportunity could now exist for primary health practitioners to help identify those at greater risk and possibly forestall subsequent neurological deterioration. PMID: 12897404 [PubMed - indexed for MEDLINE] " " Neuro Endocrinol Lett. 2004 Oct;25(5):331-9. Alzheimer disease: mercury as pathogenetic factor and apolipoprotein E as a moderator. Mutter J, Naumann J, Sadaghiani C, Schneider R, Walach H. Institute for Environmental Medicine and Hospital Epidemiology, University Hospital Freiburg, Germany. jmutter@...- freiburg.de The etiology of most cases of Alzheimer's disease (AD) is as yet unknown. Epidemiological studies suggest that environmental factors may be involved beside genetic risk factors. Some studies have shown higher mercury concentrations in brains of deceased and in blood of living patients with Alzheimer's disease. Experimental studies have found that even smallest amounts of mercury but no other metals in low concentrations were able to cause all nerve cell changes, which are typical for Alzheimer's disease. The most important genetic risk factor for sporadic Alzheimer's disease is the presence of the apolipoprotein Ee4 allele whereas the apolipoprotein Ee2 allele reduces the risk of developing Alzheimer's disease. Some investigators have suggested that apolipoprotein Ee4 has a reduced ability to bind metals like mercury and therefore explain the higher risk for Alzheimer's disease. Therapeutic approaches embrace pharmaceuticals which bind metals in the brain of patients with Alzheimer's disease. In sum, both the findings from epidemiological and demographical studies, the frequency of amalgam application in industrialized countries, clinical studies, experimental studies and the dental state of AD patients in comparison to controls suggest a decisive role for inorganic mercury in the etiology of AD. Publication Types: Review PMID: 15580166 [PubMed - indexed for MEDLINE] " Considering testing, I note that Googling turned up at least one lab that offers apolipoprotein E genotyping. Considering differences in detox protocols, I'm not sure. I'll have to try to understand how apolipoprotein E is involved in mercury transport. Thanks for raising this issue. Rich > > Rich et al, > > If this has been discussed before, forgive me (nothing came up in a > search). > > I just read this on a doctor's website, wondering if you can comment on > it: > " For example, people with an Apolipoprotein E4 Genotype lack the > ability to shuttle mercury out of the cells. As their body is unable to > detoxify, mercury accumulates in the cells and promotes disease. " > > Is this generally accepted in the mercury detox field, is there useful > testing, and would detox protocols be different for people with this > issue? > > If this topic is not appropiate to this list or has been covered, > please e-mail me. Thanks! > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 5, 2006 Report Share Posted January 5, 2006 Parents of autistic kids are looking at both apo3 and apo4 as one of the markers for poor detox of metals. > > > > Rich et al, > > > > If this has been discussed before, forgive me (nothing came up in > a > > search). > > > > I just read this on a doctor's website, wondering if you can > comment on > > it: > > " For example, people with an Apolipoprotein E4 Genotype lack the > > ability to shuttle mercury out of the cells. As their body is > unable to > > detoxify, mercury accumulates in the cells and promotes disease. " > > > > Is this generally accepted in the mercury detox field, is there > useful > > testing, and would detox protocols be different for people with > this > > issue? > > > > If this topic is not appropiate to this list or has been covered, > > please e-mail me. Thanks! > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 5, 2006 Report Share Posted January 5, 2006 Genovations.com cardio panel measures this along with the gene variants impacting glutathione status, etc.. My cardio panel through them showed I had apoe 3,4, while the most common in human population is apoe 3,3. And guess which heavy metal I consistently test highest for on both non-challenge and challenge heavy metal tests?...Lead!....I know apoe 4,4 has the highest linkage to Alzeheimer's, but anyone with a apoe 4 will be vulnerable and have brains that allow the deepest penetration of toxins and microbes according to a personalized report for my case from Dr Cheney in 2002. EDTA chelation is best suited for lead detox and given my testing profile and the great indirect indication that I have mercury toxicity as well, I opted for IV EDTA/DMPS chelation. Garden of Life's " Fungal Defense " therapy in a bottle from needs.com has been showing good signs of helping my brain too. " jill1313 " <jenbooks13@h...> wrote: > > > Parents of autistic kids are looking at both apo3 and apo4 as one of > the markers for poor detox of metals. > > > > > > Hi, shakerz25. > > > > The connection between apolipoprotein E4 genotype and problems with > > mercury detox was new to me, but I did find the following abstracts Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 5, 2006 Report Share Posted January 5, 2006 Correction...Meant to say Genovations cardio panel shows your apoe profile while their detox panel shows many gene variants impacting glutathione status. FWIW, I think its worthwhile to get all five(last I counted) of their SNPs(gene variant)panels. The results fit quite nicely with the data found in the new book, Autism: Effective Biomedical Treatments, which is fast becoming the MUST read and possible watershed book for PWME/CFIDS/Lyme treatment in 2006. " davidhall2020 " <davidhall@w...> wrote: > > Genovations.com cardio panel measures this along with the gene variants impacting glutathione status, etc.. My cardio panel through them showed I had > apoe 3,4, while the most common in human population is > apoe 3,3. > > > > And guess which heavy metal I consistently test highest for on both non-challenge and challenge heavy metal tests?...Lead!....I know apoe 4,4 has the highest linkage to Alzeheimer's, but anyone with a apoe 4 will be vulnerable and have brains that allow the deepest penetration of toxins and microbes according to a personalized report for my case from Dr Cheney in 2002. > > > > EDTA chelation is best suited for lead detox and given my testing profile and the great indirect indication that I have mercury toxicity as well, I opted for IV EDTA/DMPS chelation. Garden of Life's " Fungal Defense " therapy in a bottle from needs.com has been showing good signs of helping my brain too. > > > > > > > > > > > " jill1313 " <jenbooks13@h...> wrote: > > > > > > Parents of autistic kids are looking at both apo3 and apo4 as one of > > the markers for poor detox of metals. > > > > > > > > > > Hi, shakerz25. > > > > > > The connection between apolipoprotein E4 genotype and problems with > > > mercury detox was new to me, but I did find the following abstracts > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 5, 2006 Report Share Posted January 5, 2006 Thanx for the info . Exactly what tests did you get if you don't mind telling me? I'm going to ask for some testing next week. > > > > > > Hi, shakerz25. > > > > > > The connection between apolipoprotein E4 genotype and problems with > > > mercury detox was new to me, but I did find the following abstracts > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 5, 2006 Report Share Posted January 5, 2006 That's the DAN book I just read, correct? Can you list all the tests you are recommending? I agree, the protocol in that book is pretty brilliant and applies to all of us. The only thing some of the autism researchers are leaving out a little too much imo is borrelia. > > > > > > > > Hi, shakerz25. > > > > > > > > The connection between apolipoprotein E4 genotype and problems with > > > > mercury detox was new to me, but I did find the following abstracts > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 5, 2006 Report Share Posted January 5, 2006 Hi Jill, Message: 25 Date: Thu, 05 Jan 2006 21:55:19 -0000 From: " jill1313 " <jenbooks13@...> Subject: Re: Rich: Mercury, Apolipoprotein E4 Genotype...? > That's the DAN book I just read, correct?... the protocol in that book > is pretty brilliant and applies to > all of us. Have you figured out why Amy Yasko is not mentioned in this book? (Maybe I just haven't gotten far enough in it?) Sue , Upstate New York Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 6, 2006 Report Share Posted January 6, 2006 Hi Sue. By the way I couldn't open the URL's to that testing website you mentioned... I think, and I'm reading btw the lines, they don't like her RNA stuff. I think they don't even believe its genuine. > > Hi Jill, > > > Message: 25 > Date: Thu, 05 Jan 2006 21:55:19 -0000 > From: " jill1313 " <jenbooks13@h...> > Subject: Re: Rich: Mercury, Apolipoprotein E4 Genotype...? > > > That's the DAN book I just read, correct?... the protocol in that book > > is pretty brilliant and applies to > > all of us. > > Have you figured out why Amy Yasko is not mentioned in this book? > (Maybe I just haven't gotten far enough in it?) > > Sue , > Upstate New York > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 6, 2006 Report Share Posted January 6, 2006 Hi, . Thanks for the information. It sounds as though you've made some good choices, based on your test results. Rich > > > > > > Hi, shakerz25. > > > > > > The connection between apolipoprotein E4 genotype and problems with > > > mercury detox was new to me, but I did find the following abstracts > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 6, 2006 Report Share Posted January 6, 2006 Hi, . O.K. on the correction. I think the full set of Genovations characterizations are a worthwhile investment, too, for those who can manage it. One nice thing is that these results won't change over time, so it's an investment that should be good for a lifetime. It may be that it will become possible to characterize a large number of genetic variations for a lower cost. I can't predict this accurately, but based on the type of technology that is being used (gene chips), I think this is a good bet. I'm hopeful that we will see economies of the sort we have enjoyed with solid state electronics, which has been truly mind boggling. Rich > > Correction...Meant to say Genovations cardio panel shows your apoe profile while their detox panel shows many gene variants impacting glutathione status. > > > FWIW, I think its worthwhile to get all five(last I counted) of their SNPs(gene variant)panels. The results fit quite nicely with the data found in the new book, Autism: Effective Biomedical Treatments, which is fast becoming the MUST read and possible watershed book for PWME/CFIDS/Lyme treatment in 2006. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 6, 2006 Report Share Posted January 6, 2006 Hi, Jill. " jill1313 " <jenbooks13@h...> wrote: That's the DAN book I just read, correct? ***Yes. > Can you list all the tests you are recommending? ***Well, like I said, the five panels(which include many several gene variants) from www.genovations.com. I've listed at least a few times on this list the gene variants in which I particularly have which demonstrate predisposition to glutathione production and metabolism issues. If you want an exhaustive list of all the SNPs these panels reveal you could simply call them at their phone number at their website. I agree, the protocol in that book is pretty brilliant and applies to > all of us. The only thing some of the autism researchers are leaving > out a little too much imo is borrelia. ***Got it. My take is they probably see borrelia, along side many others infections often found in Autistics, like we PWMEs, as secondary to the primary problem of poor cellular detox/immune function caused by gene variants predisposing this. The two Polish studies cited on this list by Rich this past week on borrelia's impact on intracellular GPx seem to support their view and unveil a new leaf predictable by his. <davidhall@w...> wrote: > > > > Correction...Meant to say Genovations cardio panel shows your apoe > profile while their detox panel shows many gene variants impacting > glutathione status. > > > > > > FWIW, I think its worthwhile to get all five(last I counted) of > their SNPs(gene variant)panels. The results fit quite nicely with the > data found in the new book, Autism: Effective Biomedical Treatments, > which is fast becoming the MUST read and possible watershed book for > PWME/CFIDS/Lyme treatment in 2006. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 6, 2006 Report Share Posted January 6, 2006 , I hope you don't mind if you would repeat your gene variants for me and your interpreation of them. Really sorry, but, at whatever time you posted them I may not have been reading the list, and/or I hadn't read the DAN book yet, which has greatly impressed me. So now I would see them through a new lens and it would be helpful. I'll go google genovations and see what five panels they recommend. I get to see, after making the appointment last SEPTEMBER!, that's how long it takes, to see an immunologist who is lyme-familiar who is on my HMO, next week. I want to see if he can get any tests covered, if not, I'll pay out of pocket. I'll try to make a case for these gene variants being connected to immune function. He may be interested, I hope so, I hear he's a good guy. ly, tho, I know so many folks who were robustly healthy and borrelia knocked them flat so I still think they're underestimating borrelia. But then again, I'm 99% convinced its bioweaponized so I have my own viewpoints . Perhaps borrelia of old, naturally occurring, would be equivalent to other infections. > > > > > > Correction...Meant to say Genovations cardio panel shows your apoe > > profile while their detox panel shows many gene variants impacting > > glutathione status. > > > > > > > > > FWIW, I think its worthwhile to get all five(last I counted) of > > their SNPs(gene variant)panels. The results fit quite nicely with the > > data found in the new book, Autism: Effective Biomedical Treatments, > > which is fast becoming the MUST read and possible watershed book for > > PWME/CFIDS/Lyme treatment in 2006. > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 7, 2006 Report Share Posted January 7, 2006 What am I going to do if it is fricken ILLEGAL for me to get these tests in NY? Who else does these tests? Thanx. > > > > Correction...Meant to say Genovations cardio panel shows your apoe > profile while their detox panel shows many gene variants impacting > glutathione status. > > > > > > FWIW, I think its worthwhile to get all five(last I counted) of > their SNPs(gene variant)panels. The results fit quite nicely with > the data found in the new book, Autism: Effective Biomedical > Treatments, which is fast becoming the MUST read and possible > watershed book for PWME/CFIDS/Lyme treatment in 2006. > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 7, 2006 Report Share Posted January 7, 2006 Hi, Jill. I think has already responded about what Amy Yasko offers at www.testing4health.com There is also a company called www.sciona.com that offers genetic testing. I don't know how comprehensive it is, compared to Genovations. Rich > > What am I going to do if it is fricken ILLEGAL for me to get these > tests in NY? > Who else does these tests? Thanx. > Quote Link to comment Share on other sites More sharing options...
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