Sorry it took me so long to get back (real life obligations, darn them!:smack::D)
I have no issue with a demand for cites, it is the attitude that pisses me right off. :mad:
Anyway, for what it’s worth, here is what I managed to hobble together in my very spare “spare time”.
1: Prostaglandins Leukot Essent Fatty Acids. 2005 Nov;73(5):379-84. Links
Increased excretion of a lipid peroxidation biomarker in autism.
Ming X, Stein TP, Brimacombe M, Johnson WG, Lambert GH, Wagner GC.
Department of Neurosciences, UMDNJ-New Jersey Medical School, Newark, 07103, USA. mingxu@umdnj.edu
It is thought that autism could result from an interaction between genetic and environmental factors with oxidative stress as a potential mechanism linking the two. One genetic factor may be altered oxidative-reductive capacity. This study tested the hypothesis that children with autism have increased oxidative stress. We evaluated children with autism for the presence of two oxidative stress biomarkers. Urinary excretion of 8-hydroxy-2-deoxyguanosine (8-OHdG) and 8-isoprostane-F2alpha (8-iso-PGF2alpha) were determined in 33 children with autism and 29 healthy controls. 8-iso-PGF2alpha levels were significantly higher in children with autism. The isoprostane levels in autistic subjects were variable with a bimodal distribution. The majority of autistic subjects showed a moderate increase in isoprostane levels while a smaller group of autistic children showed dramatic increases in their isoprostane levels. There was a trend of an increase in 8-OHdG levels in children with autism but it did not reach statistical significance. There was no significant correlation between the levels of the biomarkers and vitamin intake, dietary supplements, medicine, medical disorders, or history of regression. These results suggest that the lipid peroxidation biomarker is increased in this cohort of autistic children, especially in the subgroup of autistic children.
PMID: 16081262 [PubMed - indexed for MEDLINE]
A Case-Control Study of Mercury
Burden in Children with Autistic
Spectrum Disorders
Jeff Bradstreet, M.D.
DavidA. Geier, B.A.
Jerold J. Kartzinel, M.D.
James B.Adams, Ph.D.
MarkR. Geier, M.D., Ph.D.
This study compares mercury excretion after a three-day
treatment with an oral chelating agent, meso-2,3-
dimercaptosuccinic acid (DMSA), in children with autistic spectrum
disorders and a matched control population. Overall, urinary
mercury concentrations were significantly higher in 221 children
with autistic spectrum disorders than in 18 normal controls
(Relative Increase (RI)=3.15; P < 0.0002). Additionally, vaccinated
cases showed a significantly higher urinary mercury concentration
than did vaccinated controls (RI=5.94; P < 0.005). Similar urinary
mercury concentrations were observed among matched vaccinated
and unvaccinated controls, and no association was found
between urinary cadmium or lead concentrations and autistic
spectrum disorders.
The observed urinary concentrations of mercury could
plausibly have resulted from thimerosal in childhood vaccines,
although other environmental sources and thimerosal in Rh (D)
immune globulin administered to mothers may be contributory.
Regardless of the mechanism by which children with autistic
spectrum disorders have high urinary mercury concentrations, the
DMSA treatment described in this study might be useful to diagnose their present burden of mercury…
Moreover, our findings appear to confirm previously published
epidemiologic evidence showing a direct association between
increasing mercury from thimerosal-containing childhood
vaccines and neurodevelopment disorders in children. These
studies showed that there was a two to sixfold, statistically
significant increased incidence of neurodevelopment disorders
following an additional 75-100 mcg dosage of mercury from
thimerosal-containing childhood vaccines in comparison to
thimerosal-free childhood vaccines. These studies showed doseresponse
curves demonstrating a close, statistically significant
correlation between increasing mercury doses from childhood
vaccines and childhood neurodevelopment disorders."
(a blog, but it offers a good overview of the ongoing debate, including cites of studies, so I include it)
re: From The Lancet 2002:
Mercury concentrations and metabolism in infants receiving vaccines containing thiomersal: a descriptive study.
Pichichero ME, Cernichiari E, Lopreiato J, Treanor J.
Department of Microbiology/Immunology, University of Rochester, Rochester, New York, NY, USA. michael_pichichero@urmc.rochester.edu
"Blaxil and Haley’s submission to Pediatrics:
Infant stool eliminates vaccinal mercury slowly suggesting high retention in tissue
To the editor,
In a study in The Lancet, Pichichero et al 1 argued that ethylmercury administered to infants through vaccines is eliminated rapidly from the blood and effectively excreted in stool. Our analysis of this data, combined with a more recent analysis2 of mercury excretion in baby hair suggests a more worrisome interpretation, one that offers support for the hypothesis3 linking early mercury exposures with autism.
Our calculations suggest that Pichichero et al. overstated the significance of their excretion findings. Although their data support a rapid rate of ethylmercury elimination from blood, instead of similarly rapid stool elimination, their findings demonstrate slow stool excretion in many infants, suggesting that significant amounts of ethylmercury from vaccines may be retained in infant tissue. …Blaxil and Haley’s submission to Pediatrics:
Infant stool eliminates vaccinal mercury slowly suggesting high retention in tissue
To the editor,
In a study in The Lancet, Pichichero et al 1 argued that ethylmercury administered to infants through vaccines is eliminated rapidly from the blood and effectively excreted in stool. Our analysis of this data, combined with a more recent analysis2 of mercury excretion in baby hair suggests a more worrisome interpretation, one that offers support for the hypothesis3 linking early mercury exposures with autism.
Our calculations suggest that Pichichero et al. overstated the significance of their excretion findings. Although their data support a rapid rate of ethylmercury elimination from blood, instead of similarly rapid stool elimination, their findings demonstrate slow stool excretion in many infants, suggesting that significant amounts of ethylmercury from vaccines may be retained in infant tissue. "
A newly published study of Texas school district data and industrial mercury-release data, conducted by researchers at The University of Texas Health Science Center at San Antonio, indeed shows a statistically significant link between pounds of industrial release of mercury and increased autism rates. It also shows—for the first time in scientific literature—a statistically significant association between autism risk and distance from the mercury source.
MY NOTE: Please note that mercury/thimersol has NOT been eliminated from childhood vaccines since the recent flu vaccine has served to replace most of what was eliminated from the previous schedule…if pregnant women receive this vaccine as recommended, and if infants and children receive it likewise, the odds are that they will get doses containing thimerosol and those doses are administered during fetal development, infancy, and early childhood, the most vulnerable times for mercury damage. The removal of thimerosol from childhood vaccines has oft been cited, but it has not actually happened…it was immediately replaced with thimerosol from a new recommended vaccine delivered at even more vulnerable ages. Were I a conspiracy theorist, I would conclude the timing could not have been more perfectly contrived to confound the autism statistics post “thimerosol removal”, since the worst case scenario would be eliminating thimerosol and seeing a dramatic decrease in autism as a result. But I hesitate to ascribe to conspiracy that which can be easily explained by simple ignorance/coincidence.
Geez, another thing about this board…I tire lately of being tasked to provide evidence of the obvious (as in, anyone halfway informed/educated on the issue would not demand cites but jump right into the debate, not needing to be informed of the basics first) and when I DO provide citations in support of my comments, they tend to be ignored. Not challenged with opposing citations or logically questioned but never acknowledged or referenced in the ensuing attacks which tend to be emotional and personal in nature. (and almost always from those claiming to be “Science Gods of the Universe” insert bowing icon here :rolleyes:)
But yet again, I gladly offer supporting citations, for any who might be interested. FTR, the bulk of my research is not handy at the moment, being stored and/or in a non-compatable format, so when tasked, I do a simple search and pull up the relevant information. Try it sometime. Do some basic research and get back to me.
As for the number of deaths from "VPD"s prior to vaccines, I did an article on that comparing incidence, living conditions, nutrition, etc…short summary is that serious complications and deaths from these illnesses had declined by 80 to 95% BEFORE vaccines due to improved conditions and treatments. Incidence was reduced by vaccines, but given the tendency of vaccine immunity to wane, the reductions in incidence vaccines can claim might not be such a great thing, long term.
Do you know that polio has a risk of serious complications of about 1%? And that the live polio vaccine was discontinued because it carried a higher risk than the disease itself? And that the last US polio epidemic is strongly linked to factors other than the cyclical nature of the polio virus, such as the consumption of refined sugar, the decline of breastfeeding, and exposure to pesticides and other environmental toxins? And that it is debatable whether allowing infants/young children to be exposed to polio and gain natural immunity is preferable to mass vaccination? Of course you don’t. I know; “cites, please”. sigh.
Oh, I could give them, but so much more fun to debate or discuss with someone who has already caught up. Happy fucking V-day. If you have someone anywhere near your wavelength to talk with, count yourself blessed.