Hello, haathi-ga!
Your question was more complicated to answer than I had thought it
would be! There is a lot of information on autism and mercury
chelation, but most of it is anecdotal, pushed by nutrition or
naturpathic companies and not based on scientific study. Therefore, I
focused my results only on resources that had some scientific backing.
The doctors I referenced are highly regarded by the Autism Research
Institute, and considered experts in their field. As for "pros" and
"cons", aside from the support for or against chelation, the majority
of "con" information centers on side effects or the claim of
"quackery," whereas the "pro" side claims some good results.
Statistics were the most difficult to find. I found only one
authoritative article that had statistical references for outcomes of
mercury chelation therapy. And, I could find no legitimate,
scientifically-based articles as recent as 2003.
However, I believe the following information answers your question in
terms of a scientific overview of chelation therapy for autism.
The Autism Research Institute, in a preface about their "Mercury
Detoxification Consensus Position Paper," has this to say:
http://www.autism.com/ari/mercurydetox.html
"Mercury Detoxification"
"During the past year, a number of physicians from throughout the
United States who have been working with autistic children have
reported extremely good results in improving the health and behavior
of autistic children when the mercury in the childrens bodies were
removed by a systematic process of detoxification. Some of these
physicians, who have specialized in the treatment of autistic children
for a number of years, and who have treated many hundreds of autistic
children, report that no other treatment has brought about the
remarkable improvement that they have seen in many cases of mercury
detoxification. Detoxification is not simple, and there are many
competing detoxification protocols."
"In response to this situation, the Autism Research Institute (ARI)
convened a Consensus Conference on the Detoxification of Autistic
Children in Dallas, Texas, February 9th through 11th, 2001.
** The attendees were 25 carefully selected physicians and scientists
knowledgeable about mercury and mercury detoxification. The 15
physicians present included 7 who were parents of autistic children
and who had detoxified their own children with excellent results. The
physician attendees present had treated well over 3,000 patients for
heavy metal poisoning, about 1,500 of them being autistic children.
The chemists, toxicologists, and other scientists present had a
combined total of almost 90 years of experience in studying the
toxicology of mercury." ****
=====
Physicians and Experts
**********************
I culled the following physician's names from the paper "MERCURY
DETOXIFICATION
CONSENSUS GROUP POSITION PAPER." AUTISM RESEARCH INSTITUTE. (May 2001)
http://www.autism.com/ari/mercuryconsensus.html
Sidney M. Baker, M.D.
Weston, Connecticut
Frank George, M.D.
Sun City, Arizona
Woody McGinnis, M.D.
Tucson, Arizona
John Green, M.D.
Canby, Oregon
James Neubrander, M.D.
Edison, New Jersey
Kenneth Bock, M.D.
Rhinebeck, New York
Boyd E. Haley, Ph.D.
Lexington, Kentucky
Marvin Boris, M.D.
Woodbury, New York
Stephanie Hoener, N.D.
Palm Bay, Florida
Jon Pangborn, Ph.D.
St. Charles, Illinois
Jeff Bradstreet, M.D.
Palm Beach, Florida
Amy Holmes, M.D.
Baton Rouge, Louisiana
Paul Peirsel, M.D.
Meadville, Pennsylvania
Stephanie Cave, M.D.
Baton Rouge, Louisiana
John Kucera, M.D.
Colorado Springs, Colorado
David Quig, Ph.D.
West Chicago, Illinois
Stephen M. Edelson, Ph.D.
Salem, Oregon
James R. Laidler, M.D.
Portland, Oregon
Lyn Redwood, R.N., C.R.N.P.
Tyrone, Georgia
Jane El-Dahr, M.D.
New Orleans, Louisiana
Michael Lyon, M.D.
Vancouver Island, Canada
Bernard Rimland, Ph.D.
San Diego, California
Carol Englender, M.D.
Newton Highlands, Massachusetts
Maureen H. McDonnell, R.N.
Pennington, New Jersey
Jeffrey Segal, M.D.
Greensboro, North Carolina
===
A List of US Practitioners associated with "Defeat Autism Now" can be
found at:
"DAN! Physician Referral List-Implementing the DEFEAT AUTISM
NOW!Consensus Report
http://www.cgiworker.com/danlist/danlist.html
Practioners outside the US may be found at:
http://www.cgiworker.com/danlist/dan2list.html
====
Pros" of Chelation Therapy
***************************
"Detoxification of mercury and other heavy metals by DMSA/DMPS
chelation can have marked benefit."
From "Autism, an extreme challenge to integrative medicine. Part 2:
medical management. Kidd PM. "Altern Med Rev 2002 Dec;7(6):472-99.
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12495373&dopt=Abstract
===
"Of the chelating agents available at present, DMSA (succimer, Chemet
(R) ) provides the optimal combination of safety and efficacy. DMSA
has been used extensively for nearly fifty years and is approved by
the USFDA to treat lead poisoning in children; its safety record is
exemplary 20 . There is far less experience using DMPS, especially in
children, and the adult experience with it has shown that it is
significantly more toxic than DMSA. DMPS is currently not approved for
any use by the USFDA."
"More beneficial "side effects" reported with DMSA therapy in autistic
children include rapid progression of language ability, improved
social interaction, improved eye contact, and decreased
self-stimulatory behaviors ("stimming"). Children with motor problems
have experienced significant improvement in both strength and
coordination."
"MERCURY DETOXIFICATION CONSENSUS GROUP POSITION PAPER." AUTISM
RESEARCH INSTITUTE. (May 2001)
http://www.autism.com/ari/mercuryconsensus.html
===
"Cons", or Side Effects of Mercury Chelation Therapy
***************************************************
"DMSA can cause bone marrow suppression and is potentially hepatotoxic
18 . There have been no reports yet of permanent bone marrow
suppression or liver damage, but the literature has many case reports
of significant neutropenia and thrombocytopenia during therapy with
DMSA. Prior to starting therapy, it is important that a complete blood
count (CBC) with platelet count be checked, both to provide a baseline
as well as to detect any pre-existing abnormalities. Blood levels of
liver transaminases (ALT and AST) are also important for the same
reasons."
"DMSA is primarily excreted in the urine 19 , so kidney dysfunction
will cause it to accumulate in the blood. To prevent serious toxicity,
it is important to detect any decreased renal function prior to
starting therapy. In the absence of any signs or symptoms of renal
insufficiency, blood urea nitrogen (BUN) and creatinine levels should
be adequate to document normal renal function. If there are any
reasons to suspect renal insufficiency, creatinine clearance should be
measured. Periodic checks of blood urea nitrogen and creatinine should
also be performed when other blood studies are done."
"Common side effects of DMSA are nausea, diarrhea, anorexia,
flatulence and fatigue. If these become serious enough, reducing the
dose will usually make the symptoms tolerable. Occasionally, patients
develop a maculopapular rash during treatment; this should not to be
confused with an allergic reaction 27 . Some autistic children are
reported to experience a transient regression in language and behavior
during and shortly after treatment. Reducing the dose may also make
these symptoms less bothersome. Clinical experience suggests that most
children who experience regression at the start of therapy will have
less regression with each subsequent cycle of treatment."
"Serious side effects of DMSA are extremely rare and include allergic
reaction, toxic epidermal necrolysis (TEN) and erythema multiforme
(Stevens-Johnson syndrome) a. Potentially dangerous neutropenia and
thrombocytopenia may also occur 28 . While reducing the dose may
reduce the severity of the neutropenia and thrombocytopenia, truly
dangerous reductions in cell count are a contraindication to continued
therapy without a compelling reason to do so. Obviously, allergic
reaction, TEN and Stevens-Johnson syndrome are absolute
contraindications to continued therapy."
"A number of children have shown significant improvement while taking
the DMSA, which regresses when they stop, even for the "rest period"
of each cycle. These children need to be dealt with on a case-by-case
basis, since there is insufficient clinical experience so far to
recommend a course of action."
"MERCURY DETOXIFICATION CONSENSUS GROUP POSITION PAPER." AUTISM
RESEARCH INSTITUTE. (May 2001)
http://www.autism.com/ari/mercuryconsensus.html
==
According to "Autism and Mercury Detoxification," by P. Kane, Ph.D.
and J. Mercola, D.O..
Optimal Wellness Center. Issue 173. (10/1/2000)
http://autism.about.com/gi/dynamic/offsite.htm?site=http%3A%2F%2Fwww.mercola.com%2F2000%2Foct%2F1%2Fmercury_autism.htm
"Some chelationists allege that childhood autism is caused by mercury
toxicity and treatable with chelation. However, there is no scientific
evidence that autism has a toxic cause or is associated with abnormal
levels of heavy metals."
Read "NCAHF Policy Statement on Chelation Therapy." National Council
Against Health Fraud.
(10/7/2002)
http://www.ncahf.org/policy/chelation.html
===
".... some natural medicine clinicians have some serious concerns
about the use of DMSA. There have been cases of:
seizures
increased self-stimming
and compromised central nervous system function in some children
DMSA and Mercury Redistribution To The Brain
"It appears that DMSA and lipoic acid can create tissue redistribution
of mercury as decreasing Hg levels in the kidney (the organ
accumulating Hg most abundantly) increases Hg concentrations of Hg in
blood, brain, lung, heart, muscle and liver (Gregus et al)."
"Natural medical physicians throughout the US have reported MS
symptoms in adults and intractable seizures in pediatric patients with
high dose and extended use of DMSA (2, 3-dimercaptosuccinic acid),
Chemet or Succimer."
Other Problems With DMSA
"Extended use of DMSA can cause mild to moderate neutropenia with
increased SGOT, SGPT, Platelet count, Cholesterol, Alkaline
Phosphatase and Blood Urea Nitrogen (BUN). Adverse reactions to DMSA
include ataxia, convulsions, rash, nausea, diarrhea, anorexia,
headache, dizziness, sensorimotor neuropathy, decreased urination,
arrhythmia, infection. Zinc excretion doubles during the
administration of DMSA. Patients must be kept hydrated as renal
function can be compromised."
"For the above described reasons in all good conscious we can not
recommend the use of DMSA for the treatment of mercury toxic pediatric
patients."
"Approaching the fragile brain architecture of young children with
autism, PDD and seizure disorders brings about tremendous
responsibility in protecting the children from invasive interventions
that risk alteration in brain function."
===
Success Rate Statistics
************************
The article, "Chelation of Mercury for the Treatment of Autism," Amy
S. Holmes M.D. (no date) at
http://healing-arts.org/children/holmes.htm has some limited
statistics:
Early Results:
"We currently have over 500 autistic patients under treatment with
DMSA ranging in age from 1 to 24 years old. In general, we do not
expect to see any behavioral, language, or social improvements until
at least some of the CNS mercury has been removed. As of 1/15/01, we
had 85 patients who had finished DMSA alone and had completed at least
4 months of DMSA + lipoic acid. The results of treatment in these
patients are presented below:
n = 85 Improvement (%)
Age Number Marked Moderate Slight None
1-5 40 35 39 15 11
6-12 25 4 28 52 16
13-17 16 0 6 68 26
18+ 4 0 0 25 75
Once lipoic acid is added, we usually track mercury excretion via
tests of fecal mercury. We have noticed a large dependence of
excretion on age of patient with the younger patients excreting much
more mercury than the older patients. We think this difference in
rapidity of excretion may explain the differences in response between
the various age groups.
We have 6 patients, all 1 to 2 years of age who are finished with
treatment by measurements of urinary and fecal mercury excretion.
These 6 patients are "normal" by parent reports and repeat
psychological testing. We have no children over the age of 2 who are
finished with treatment. The rapidity of excretion seems to decrease
markedly with each additional year of age. There are several children,
mostly in the younger age groups, who have made remarkable progress to
the point of being able to be mainstreamed in school, but who are
still have some "oddities" of behavior - none of these children have
completed treatment yet.
These are very early results, but appear very promising. As more data
is gathered, outcomes will be better able to be predicted, including
length of treatment as well as ultimate prognosis.
===
Additional Reading
******************
"Autistic Children Show Improvement With Detoxification." BW
HealthWire (4/26/2002)
http://www.testfoundation.org/autismdetox.htm
(Describes benefits of oral clathration)
==========================
I sincerely hope the above information provides a good starting point
for information and an answer to your question. If I can be of further
help, or the links do not work, please let me know in a clarification.
I will be happy to help!
Thanks!
umiat-ga
Google Search Strategy
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