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By News Staff | January 30th 2008 01:08 PM | 2 comments | Print | E-mail | Track Comments
February’s issue of Pediatrics offers a study saying there is reason to rethink blaming the spike in autism diagnoses on thimerosal, a mercury-containing preservative routinely used in several childhood vaccines until the late ‘90s.

The research from the University of Rochester suggests that infants’ bodies expel the thimerosal mercury much faster than originally thought – thereby leaving little chance for a progressive build up of the toxic metal.

Some parents and pediatricians believe that the series of thimerosal-containing shots many infants received in the 1990s, when the average number of vaccines kids received increased sharply, had put them at risk for developmental disorders.

Thimerosal, hailed for its bacteria-killing properties, had been a vaccine staple ingredient since the 1930s but when the Environmental Protection Agency announced in 1999 that the cumulative exposure children typically received in vaccines might exceed a safe level for intake based on methyl mercury statistics, public health officials, together with the American Academy of Pediatrics, recommended its removal.

“Thimerosal has been used for decades, but the surge in vaccinations caused fear that possible accumulations of ethyl mercury, the kind in thimerosal, might exceed safe levels – at least, when based on the stringent risk guidelines applied to its better-understood chemical cousin, methyl mercury, which is associated with eating fish,” said Michael Pichichero, M.D., professor of Microbiology/Immunology, Pediatrics and Medicine at the University of Rochester and the study’s main author.

Scientists are learning that the two mercury species actually behave quite differently.

Previous research conducted in Seattle just a few years ago demonstrated that the ethyl mercury has a more difficult time crossing the blood-brain barrier, posing even less toxic risk than methyl mercury. This is especially telling, since even methyl mercury itself has also proven rather benign at low levels. In fact, just a few years ago, a Rochester study showed that children born to mothers-to-be who ate an average of 12 meals of fish a week – about 10 times the amount that the average U.S. citizen eats – showed no harmful symptoms.

And now, the most recent research from Rochester unveils further differences between the two types of mercury: the body rids the kind found in thimerosal more that 10 times faster than it removes the kind one might encounter in a Friday night fish fry.

In the Rochester study, 216 infants from R. Gutierrez Children’s Hospital (in Buenos Aires, Argentina, where thimerosal is still routinely used in vaccines) were divided into three age groups to have their blood-mercury levels tested both before and after shots were administered at either their newborn, 2- or 6-month checkup. Researchers learned that, in all three age groups, the half-life of ethyl mercury in the blood – or, the time it takes for the body to dispose of half the mercury, and then another half, and so on – was measured to be 3.7 days. That’s a far cry from the blood half-life of methyl mercury, which is 44 days.

“Until recently, that longer half-life was assumed to be the rule for both types of mercury. Now it’s obvious that ethyl mercury’s short half-life prevents toxic build-up from occurring. It’s just gone too fast,” Pichichero said.

To illustrate, researchers cite that infants in the 6-month-old group – who, in their lifetimes, had encountered more total ethyl mercury that any other group studied – still had the same pre-vaccination blood-mercury levels before their checkups as most 2-month-olds had before theirs. This suggests that, before each round of shots, the mercury has plenty of time to be cleared.

The study also showed that ethyl mercury was nearly undetectable in urine samples; instead, it seemed that most of it was eliminated via stools. That’s good, because mercury in large amounts is toxic to kidneys – yet in the study sample, there was no evidence of any harm to renal tissues.

These findings come in the wake of recent news from the California Department of Health, which reported last month that autism rates continue to mushroom in spite of the widespread removal of thimerosal from most U.S. childhood vaccines in 2001, though it continues to be used in vaccines used elsewhere in the world.

“Though it’s reassuring to affirm that these immunizations have always been safe, our findings really have greater implications for world health,” Pichichero said. “Replacing the thimerosal in vaccines globally would put these vaccines beyond what the world community could afford for its children. It’s a relief we haven’t cause to do that.”

This research was supported by the National Institute of Allergy and Infectious Diseases of the National Institutes of Health. It was performed in conjunction with investigators Angela Gentile, M.D, Norberto Giglio, M.D., and Veronica Umido, M.D., of R. Gutierrez Children’s Hospital in Buenos Aires; Carlos Gotelli, Ph.D., and Mariano Gotelli, Ph.D., of the Center of Toxicology Research in Buenos Aires; Lihan Yan, M.S., of EMMES Corp in Rockville, Maryland; and Thomas Clarkson, Ph.D., Elsa Cernichiari, M.S., Grazyna Zareba, Ph.D., and John Treanor, M.D., of the University of Rochester.

Comments

Autism is one of what I believe are a number of what are called passive developmental disorders- and autism is the most common. Autism is a disability caused by a brain development disorder of unknown cause, yet some suspect the cause is some sort of neurological dysfunction. Usually, symptoms of the disease present themselves before the toddler reaches the age of three. Before Autism was more understood, others labeled them as childhood schizophrenia or as having a psychosis or mental retardation.
Out of 16 related characteristics, eight must be present to be considered autistic, according to others. As with all passive developmental disorders, the person expresses language, social, and behavioral difficulties. Treatment includes what are called psychotropic medications that delay the progression of the disorder, as well as relieve some of the symptoms of one who is autistic. Behavioral therapy is common as a treatment regimen as well. Boys get Autism much more than girls.
Then there is the controversy between many who claim that thimerosal- a preservative containing mercury, which is a neurotoxin that was used in vaccines until 2001, was the catalyst for autism in children. Over 5000 lawsuits have been filed because of this belief, and some have been successful for the plaintiff. Yet most agree the correlation between thimersal and autism is void of scientific merit. Furthermore, the cases of autism have not decreased since the preservative was discontinued in 2001.
Aside from Autism, the other four passive developmental disorders are known as autism spectrum disorders.
Asperger’s Syndrome is more common than autism, and the symptoms are milder, as there is minimal delay in language abilities, if at all. What is expressed with Asperger’s syndrome is mild autistic symptoms. In time, the patient may express atypical personality disorders, though. While intelligence is within normal limits with the Asperger’s patient, social interactions and abilities preset difficulty for such a patient. As with Autism, medications and behavioral therapy are treatment regimens with one with this syndrome
Rett’s Syndrome or disorder presents with not only atypical behavior, but also suffers from restricted physical growth and movement. There is cognitive and social impairment as well. The disorder affects mostly girls, and the cause is due to a gene mutation.
Chldhood Disintegrative disorder is rare, and is 10 times less common than autism. The disorder has a late onset with mild autistic symptoms. The disorder affects mostly boys, and regression is sudden and possible with this disorder. Skills lost with this disorder may be language, social, self-care, as well as play or motor skills. Decreased function or impairment with this disorder may include social skills and behavioral flaws. Central Nervous System pathology is a suspected cause of this disorder.
Finally, there are passive development disorders that are not otherwise specified. This may include atypical autism, for example. Yet as with the rest of types of these disorders, the symptoms vary in their intensity, and the range of abilities of these developmental disorders vary widely as well. Medicinal treatment along with cognitive and behavioral therapy prove to be most beneficial for all the different types of Passive Development Disorders that unfortunately exist for unknown reasons,

Dan Abshear

The piece of information that this article/study doesn't include is how much lead was in the systems of the primates. Since lead potentiates with mercury making it more than 100 X more toxic that mercury alone,
it is a very important factor. Also, I am curious as to when the blood brain barrier forms in primates. Same as humans - around 2 years of age?
I am also skeptical that "methyl mercury itself has also proven rather benign at low levels". At very least, it is a controversial issue with conflicting data to date. The fact that Canada and the US have established different levels of exposure which each county deems safe speaks volumes.
There is value here though. Until the autism community understands the role of lead exposure in autism, and begins to look broader for other sources of mercury, they are chasing their tails with no resolution in sight.
I have written a book on lead which touches on potentiation, and the lead-mercury connection if anyone is interested. Lead Babies. ISBN 978-1-60164-192-2
by Cerazy and Cottingham

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