The latest attempt to link vaccines and the mercury within them (not that there is any mercury within them any more) with the causation of autism seems to be laid out here.
According to David Geier, the father-son team first became interested in this question after viewing a poster in which Dr. Boyd Haley showed how the addition of even a small amount of testosterone greatly enhanced the destructive power of mercury.
Through the work of Dr. Jill James, the Geiers were aware that people with autism had significantly lower levels of glutathione. In their investigations the Geiers found that testosterone blocks the body’s ability to make glutathione and that mercury binds to glutathione, thus inactivating whatever stores the body may already have.
According to the Geiers mercury also raises testosterone levels, while dramatically lowering glutathione. At special risk would be those individuals who have a family history of low estrogen and high testosterone. The Geiers’ theory might tie together several disparate findings and give hope for those children who have not fully recovered through bio-medical interventions.
A known side-effect of high testosterone is precocious puberty, or the early development of adult features in children. When the Geiers went looking for signs of precocious puberty in the autistic children in their clinic they found it in approximately 80% of their patients.
According to the Breast Cancer Fund, over the past forty years the age of puberty in girls has dropped one to two years. The Geiers believe this is a population-wide effect of mercury from the vaccines. When the Geiers tested seventy children with autism for abnormal testosterone levels they found results outside the normal range in approximately one-quarter to one-third of their patients.
Now, no, I’m not a scientist (at least, not a physical scientist) so I’m not going to try and either prove or disprove this thesis. I’ll leave that to the people with the appropriate qualifications. That they’re discussing chelation as a treatment for autism makes me think it’s unlikely at the best to be true, but that’s not my point in mentioning it here.
Rather, it’s the way in which they seem to think that this post birth, indeed, post vaccine, connection between mercury and autism has anything at all to do with Simon Baron-Cohen’s views on autism being a product of the extreme male brain.
Just one little thing about Baron-Cohen’s ideas: he does think he’s found the explanation for many or most cases of autism. That hesitancy is because autism isn’t so much a disease or a genetic condition as it is a set of symptoms. Those who have the symptoms are said to be on the autistic spectrum: but that doesn’t mean that all occurences of said symptoms have the same cause. We know very well that there are certain genetic conditions which produce the same or very similar symptoms just as we also know that most showing the symptoms don’t have those genetic conditions.
But the little thing: while he thinks he’s along the right lines he most certainly has not ruled out there being either environmental causes for some cases or even all. It could be that there is a predisposition which needs a trigger to cause the full syndrome. I might add that he doesn’t think that it’s mercury in vaccines, as that has been removed from vaccines in different countries at different times and the incidence of autism hasn’t fallen after that removal in any of them.
But on to the major point here: Baron-Cohen’s connection between testosterone and autism, that extreme male brain idea, is something to do with in utero exposure, that is, fetal exposure to testosterone. As the brain develops in utero the various hormones it is exposed to do indeed change the paths of development: this is why pregnant women are advised so strongly not to drink, or why sufficient folic acid needs to be in the mother’s diet to avoid spina bifida. This creation of the extreme male brain is nothing to do with testosterone levels in the bloodstream post partum, nothing to do with the receptors for testosterone in the child (if it were we’d be having female autists growing beards). The theory is about what happens in the womb, not anything that happens after it.
Now, as I say, I’m not about to declare the theory put forward in the linked post to be incorrect, even if I think it is. Rather, I just want to point out that you can’t use Simon Baron-Cohen’s theory to support it, not unless you’ve got some interesting form of time machine. He is saying that autism is connected with fetal exposure to testosterone, not to the levels of testosterone (or mercury) that the child is exposed to after birth.