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DHEA for Lupus

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Thank you I will check into DHEA

" Namaste "

Tia

[ ] DHEA for Lupus

Hi Tia,

Sorry to hear about you multiple health problems. DHEA is a master hormone

that has been used successfully with Lupus. See Medline article below:

: _Autoimmunity. _ (javascript: AL_get(this, 'jour', 'Autoimmunity. ');) 2005

Nov;38(7):531- 40.

(http://www.ncbi. nlm.nih.gov/ entrez/utils/ fref.fcgi? itool=AbstractPl

us-def & PrId= 3396 & uid= 16373258 & db=pubmed & url=http: //taylorandfranc is.met

apress.com/Index/ 10.1080/08916930 500285550) _Links_

(javascript: PopUpMenu2_ Set(Menu16373258 );)

Effects of dehydroepiandroster one supplement on health-related quality of

life in glucocorticoid treated female patients with systemic lupus

erythematosus.

* _Nordmark G_

(http://www.ncbi. nlm.nih.gov/ entrez/query. fcgi?db=pubmed & cmd=Search &

itool=pubmed_ AbstractPlus & term= " Nordmark+G " [Author]) ,

* _Bengtsson C_

(http://www.ncbi. nlm.nih.gov/ entrez/query. fcgi?db=pubmed & cmd=Search &

itool=pubmed_ AbstractPlus & term= " Bengtsson+C " [Author]) ,

* _Larsson A_

(http://www.ncbi. nlm.nih.gov/ entrez/query. fcgi?db=pubmed & cmd=Search &

itool=pubmed_ AbstractPlus & term= " Larsson+A " [ Author]) ,

* _Karlsson FA_

(http://www.ncbi. nlm.nih.gov/ entrez/query. fcgi?db=pubmed & cmd=Search &

itool=pubmed_ AbstractPlus & term= " Karlsson+FA " [Author]) ,

* _Sturfelt G_

(http://www.ncbi. nlm.nih.gov/ entrez/query. fcgi?db=pubmed & cmd=Search &

itool=pubmed_ AbstractPlus & term= " Sturfelt+G " [Author]) ,

* _Ronnblom L_

(http://www.ncbi. nlm.nih.gov/ entrez/query. fcgi?db=pubmed & cmd=Search &

itool=pubmed_ AbstractPlus & term= " Ronnblom+L " [Author]) .

Department of Medical Sciences, Section of Rheumatology, University

Hospital, Uppsala, Sweden. gunnel.nordmark@ medsci.uu. se

The objective of this study was to evaluate the efficacy of low dose

dehydroepiandroster one (DHEA) on health-related quality of life (HRQOL) in

glucocorticoid treated female patients with systemic lupus erythematosus (SLE).

Forty

one women ( >or= 5 mg prednisolone/ day) were included in a double-blind,

randomized, placebo-controlled study for 6 months where DHEA was given at 30

mg/20 mg ( <or= 45/ >or= 46 years) daily, or placebo, followed by 6 months open

DHEA treatment to all patients. HRQOL was assessed at baseline, 6 and 12

months, using four validated questionnaires and the patients' partners completed

a

questionnaire assessing mood and behaviour at 6 months. DHEA treatment

increased serum levels of sulphated DHEA from subnormal to normal. The DHEA

group

improved in SF-36 " role emotional " and HSCL-56 total score (both p<0.05).

During open DHEA treatment, the former placebo group improved in SF-36 " mental

health " (p<0.05) with a tendency for improvement in HSCL-56 total score

(p=0.10). Both groups improved in McCoy's Sex Scale during active treatment

(p<0.05). DHEA replacement decreased high-density lipoprotein (HDL) cholesterol

and

increased insulin-like growth factor I (IGF-I) and haematocrit. There were no

effects on bone density or disease activity and no serious adverse events.

Side effects were mild. We conclude that low dose DHEA treatment improves

HRQOL with regard to mental well-being and sexuality and can be offered to women

with SLE where mental distress and/or impaired sexuality constitutes a

problem.

PMID: 16373258 [PubMed - indexed for MEDLINE]

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  • 1 month later...

Hi Health Activists,

Last week I was at the library reading the Journal of the American Medical

Association (JAMA) for January 10.1007 which had an article on the Research

on the Causes and Treatments for Lupus. The full name of the disease is called

Systemic Lupus Erythematosis (SLE), characterized by the immune system

attacking itself for no apparent reason.

Since their is plentiful funding for Genetic Research, a large portion of

the research has been done on the possible genetic factors causing the disease

to express itself. It seems to occur more frequently in middle aged women for

some reason. The researchers seem to be perplexed and frustrated with the

limitations of the current treatments which usually consist of Non-Steroidal

Anti Inflammatory Drugs (NSAIDS), Immunosuppressive Drugs and Cortocosteroids.

All of these have unpleasant side effects, that can be serious.

Despite these dangerous side effects, very little work and even less

publicity has been given to the treatment with Dehydroepiandrosterone (DHEA).

DHEA

is a hormone sold as a dietary supplement in the United States. It has a very

safe profile in prior use, but since it is a hormone, many holistic doctors

have felt that, if the patient has or is at high risk for a reproductive

cancer, it might be advisable to avoid DHEA or make sure an integrative

practitioner monitors the level very closely. DHEA has been very successful in

the

treatment of Lupus (SLE) and I accordingly wrote to JAMA citing a few of these

studies. Sine I do not expect them to publish my letter I felt, it might get

some attention if I sent you a copy.

To The Editor:

The article " Researchers Probe Lupus Causes,Treatments by Hampton

appearing in the the January 10,2007 issue concentrates on the interesting

developments in possible genetic causation and theoretical mechanisms, but

overlooks the remarkably successful treatment using Dehydroepiandrosterone

(DHEA).

The author, expresses concern at the " puzzles and frustration " of those seeking

diagnostic and treatment breakthroughs, but fails to acknowledge the large

body of documented medical literature supporting this treatment with DHEA.

Unfortunately it is only known to patients who are sophisticated enough to do

their own research of the medical literature.

In a double blind placebo controlled clinical trial using 200 mg of DHEA

researchers found " Dehydroepiandrosterone suppresses Interleukin 10 synthesis

in Women with Systemic lupus erythematosis " by Chang,DM et al., in the Ann

Rheum Dis,2004,Dec;63(12):1623-6. DHEA significantly lupus flares.

In another double blind placebo controlled study of " Dehydoepiandrosterone

treatment of women with mild to moderate systemic lupus erythematosis: a

multicenter randomized double blind, placebo controlled trial " Chang,DM et al.

writing in Arthritis Rheum, 2002 Nov;46(11):2924-7 using 200 mg of DHEA found

that patient global assessment of improvement in the DHEA group was

statistically greater than in the placebo group.The patient having adverse

flares was

significantly less in the DHEA group.

While these were done with mild to moderate lupus, van Vollenhoven RF.et al,

conducted a " Double blind ,placebo controlled clinical trial of

dehydroepiandrosterone in severe systemic lupus erythematosis " .Their results

were

published in Lupus,1999;8(3):169-70. In a trial of 21 patients with severe

lupus,

a group that received 200 mg was felt by researchers to have more severe

symptoms at baseline. DHEA was given in addition to conventional treatment

with

corticosteroids and immunosuppressives for 6 months, followed by a 6 month

open label period. 19 patients were available for evaluation at 6 months. The

primary outcome was a prospectively defined responder analysis of improvement.

The results showed that 7 of 9 responders in the DHEA compared to 4 of 10

patients on placebo(receiving conventional therapy). Of the secondary outcome,

measuring mean improvement of SLE disease activity index (SLE-DAI) was

greater in the DHEA group.(-10.3+/-3.1 vs. -3.9+/-1.4, P less than 0.07.

Despite

these very promising results, the author inexplicably undervalues his

positive results on that the beneficial effect of DHEA and if researchers are

too

lazy to read the full results, they may be led to believe that DHEA is not

that effective. All of these studies were done overseas, but the treatment of

serious disease should not be effected by this parochialism in the age of

instant communications.( Actually the last study by van Vollenhoven might have

been done in the US, he is a professor at Stanford University Medical

Center-AG)

Arnold Gore

New York,NY

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  • 2 weeks later...

Hi :

I have aproblemwith hair loss. I have had my thyroid, and testosterone checked

and it is alwas normal. I have been lossing my hair for a long time. ( now it

is showing) Any other ideas as to what I should check? I am 53 and post

menopause

Any info is appreciated,

<mindcb45@...> wrote:

Arnold,

Healthy women who want to try DHEA should start with 1mg or 3mg every other day

and talk to their doctors as well. They would only try it if they were having

hormonal imbalances in the first place. DHEA raises the testosterone levels

amoung many other things in the woman's hormonal system. Anyone who wants to try

this hormone should understand where it is in a complicated chain of reactions.

Pregnenolone starts the cascade of reactions. Ray Sahelian, MD's book, " Mind

Boosters " has a very clear explanation of this process.

The story is much different with men. I have been taking 50 mg of DHEA for more

than 23 years. I do not take additional pregnenolone however. I would be very

careful to add pregnenolone if you have seizures because of all the different

hormonal interactions that take place. DHEA is down line from the pregnenolone

and does not affect as many hormones. Also, I was taking the DHEA before my

seizures returned--many years before--so I have just continued with it.

Sahelian's web site has a good discussion about DHEA from many people who have

tried it. Both men and women.

[ ] DHEA for Lupus

Hi Health Activists,

Last week I was at the library reading the Journal of the American Medical

Association (JAMA) for January 10.1007 which had an article on the Research

on the Causes and Treatments for Lupus. The full name of the disease is called

Systemic Lupus Erythematosis (SLE), characterized by the immune system

attacking itself for no apparent reason.

Since their is plentiful funding for Genetic Research, a large portion of

the research has been done on the possible genetic factors causing the disease

to express itself. It seems to occur more frequently in middle aged women for

some reason. The researchers seem to be perplexed and frustrated with the

limitations of the current treatments which usually consist of Non-Steroidal

Anti Inflammatory Drugs (NSAIDS), Immunosuppressive Drugs and Cortocosteroids.

All of these have unpleasant side effects, that can be serious.

Despite these dangerous side effects, very little work and even less

publicity has been given to the treatment with Dehydroepiandroster one (DHEA).

DHEA

is a hormone sold as a dietary supplement in the United States. It has a very

safe profile in prior use, but since it is a hormone, many holistic doctors

have felt that, if the patient has or is at high risk for a reproductive

cancer, it might be advisable to avoid DHEA or make sure an integrative

practitioner monitors the level very closely. DHEA has been very successful in

the

treatment of Lupus (SLE) and I accordingly wrote to JAMA citing a few of these

studies. Sine I do not expect them to publish my letter I felt, it might get

some attention if I sent you a copy.

To The Editor:

The article " Researchers Probe Lupus Causes,Treatments by Hampton

appearing in the the January 10,2007 issue concentrates on the interesting

developments in possible genetic causation and theoretical mechanisms, but

overlooks the remarkably successful treatment using Dehydroepiandroster one

(DHEA).

The author, expresses concern at the " puzzles and frustration " of those seeking

diagnostic and treatment breakthroughs, but fails to acknowledge the large

body of documented medical literature supporting this treatment with DHEA.

Unfortunately it is only known to patients who are sophisticated enough to do

their own research of the medical literature.

In a double blind placebo controlled clinical trial using 200 mg of DHEA

researchers found " Dehydroepiandroste rone suppresses Interleukin 10 synthesis

in Women with Systemic lupus erythematosis " by Chang,DM et al., in the Ann

Rheum Dis,2004,Dec; 63(12):1623- 6. DHEA significantly lupus flares.

In another double blind placebo controlled study of " Dehydoepiandroster one

treatment of women with mild to moderate systemic lupus erythematosis: a

multicenter randomized double blind, placebo controlled trial " Chang,DM et al.

writing in Arthritis Rheum, 2002 Nov;46(11):2924- 7 using 200 mg of DHEA found

that patient global assessment of improvement in the DHEA group was

statistically greater than in the placebo group.The patient having adverse

flares was

significantly less in the DHEA group.

While these were done with mild to moderate lupus, van Vollenhoven RF.et al,

conducted a " Double blind ,placebo controlled clinical trial of

dehydroepiandroster one in severe systemic lupus erythematosis " .Their results

were

published in Lupus,1999;8( 3):169-70. In a trial of 21 patients with severe

lupus,

a group that received 200 mg was felt by researchers to have more severe

symptoms at baseline. DHEA was given in addition to conventional treatment with

corticosteroids and immunosuppressives for 6 months, followed by a 6 month

open label period. 19 patients were available for evaluation at 6 months. The

primary outcome was a prospectively defined responder analysis of improvement.

The results showed that 7 of 9 responders in the DHEA compared to 4 of 10

patients on placebo(receiving conventional therapy). Of the secondary outcome,

measuring mean improvement of SLE disease activity index (SLE-DAI) was

greater in the DHEA group.(-10.3+ /-3.1 vs. -3.9+/-1.4, P less than 0.07.

Despite

these very promising results, the author inexplicably undervalues his

positive results on that the beneficial effect of DHEA and if researchers are

too

lazy to read the full results, they may be led to believe that DHEA is not

that effective. All of these studies were done overseas, but the treatment of

serious disease should not be effected by this parochialism in the age of

instant communications. ( Actually the last study by van Vollenhoven might have

been done in the US, he is a professor at Stanford University Medical

Center-AG)

Arnold Gore

New York,NY

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I was loosing a lot of hair for the longest time until I did a colon cleans

from www.drnatura.com the only one I found that actually worked. My hair would

come out in handfuls and it hasn't done that in over 8 months now. Most tests

come out normal because they haven't been updated since the 70's done off of

military men.

Remember toxins cause a lot in all areas of our body, if you have toxic organs

you won't get the vitamins you need to have your body work right.

" Namaste "

Tia

[ ] DHEA for Lupus

Hi Health Activists,

Last week I was at the library reading the Journal of the American Medical

Association (JAMA) for January 10.1007 which had an article on the Research

on the Causes and Treatments for Lupus. The full name of the disease is called

Systemic Lupus Erythematosis (SLE), characterized by the immune system

attacking itself for no apparent reason.

Since their is plentiful funding for Genetic Research, a large portion of

the research has been done on the possible genetic factors causing the disease

to express itself. It seems to occur more frequently in middle aged women for

some reason. The researchers seem to be perplexed and frustrated with the

limitations of the current treatments which usually consist of Non-Steroidal

Anti Inflammatory Drugs (NSAIDS), Immunosuppressive Drugs and Cortocosteroids.

All of these have unpleasant side effects, that can be serious.

Despite these dangerous side effects, very little work and even less

publicity has been given to the treatment with Dehydroepiandroster one (DHEA).

DHEA

is a hormone sold as a dietary supplement in the United States. It has a very

safe profile in prior use, but since it is a hormone, many holistic doctors

have felt that, if the patient has or is at high risk for a reproductive

cancer, it might be advisable to avoid DHEA or make sure an integrative

practitioner monitors the level very closely. DHEA has been very successful in

the

treatment of Lupus (SLE) and I accordingly wrote to JAMA citing a few of these

studies. Sine I do not expect them to publish my letter I felt, it might get

some attention if I sent you a copy.

To The Editor:

The article " Researchers Probe Lupus Causes,Treatments by Hampton

appearing in the the January 10,2007 issue concentrates on the interesting

developments in possible genetic causation and theoretical mechanisms, but

overlooks the remarkably successful treatment using Dehydroepiandroster one

(DHEA).

The author, expresses concern at the " puzzles and frustration " of those seeking

diagnostic and treatment breakthroughs, but fails to acknowledge the large

body of documented medical literature supporting this treatment with DHEA.

Unfortunately it is only known to patients who are sophisticated enough to do

their own research of the medical literature.

In a double blind placebo controlled clinical trial using 200 mg of DHEA

researchers found " Dehydroepiandroste rone suppresses Interleukin 10 synthesis

in Women with Systemic lupus erythematosis " by Chang,DM et al., in the Ann

Rheum Dis,2004,Dec; 63(12):1623- 6. DHEA significantly lupus flares.

In another double blind placebo controlled study of " Dehydoepiandroster one

treatment of women with mild to moderate systemic lupus erythematosis: a

multicenter randomized double blind, placebo controlled trial " Chang,DM et al.

writing in Arthritis Rheum, 2002 Nov;46(11):2924- 7 using 200 mg of DHEA found

that patient global assessment of improvement in the DHEA group was

statistically greater than in the placebo group.The patient having adverse

flares was

significantly less in the DHEA group.

While these were done with mild to moderate lupus, van Vollenhoven RF.et al,

conducted a " Double blind ,placebo controlled clinical trial of

dehydroepiandroster one in severe systemic lupus erythematosis " .Their results

were

published in Lupus,1999;8( 3):169-70. In a trial of 21 patients with severe

lupus,

a group that received 200 mg was felt by researchers to have more severe

symptoms at baseline. DHEA was given in addition to conventional treatment with

corticosteroids and immunosuppressives for 6 months, followed by a 6 month

open label period. 19 patients were available for evaluation at 6 months. The

primary outcome was a prospectively defined responder analysis of improvement.

The results showed that 7 of 9 responders in the DHEA compared to 4 of 10

patients on placebo(receiving conventional therapy). Of the secondary outcome,

measuring mean improvement of SLE disease activity index (SLE-DAI) was

greater in the DHEA group.(-10.3+ /-3.1 vs. -3.9+/-1.4, P less than 0.07.

Despite

these very promising results, the author inexplicably undervalues his

positive results on that the beneficial effect of DHEA and if researchers are

too

lazy to read the full results, they may be led to believe that DHEA is not

that effective. All of these studies were done overseas, but the treatment of

serious disease should not be effected by this parochialism in the age of

instant communications. ( Actually the last study by van Vollenhoven might have

been done in the US, he is a professor at Stanford University Medical

Center-AG)

Arnold Gore

New York,NY

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