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Dental
Amalgam and Mercury Levels in Autopsy Tissues:
Food for Thought.
American Journal of Forensic Medicine & Pathology. 27(1):42-45,
March 2006.
Guzzi, Gianpaolo DDS *; Grandi, Marco MD +; Cattaneo, Cristina PhD;
Calza, Stefano MSc [S]; Minoia, Claudio BSc; Ronchi, Anna BSc; Gatti,
Anna BSc ; Severi, Gianluca PhD
Abstract: Eighteen cadavers from routine autopsy casework
were subject to a study of tissue levels of total mercury in brain,
thyroid, and kidney samples by atomic absorption. On these same
cadavers, all dental amalgam fillings (the most important source
of inorganic mercury exposure in the general population, according
to the World Health Organization (WHO) were charted. Total mercury
levels were significantly higher in subjects with a greater number
of occlusal amalgam surfaces (>12) compared with those with fewer
occlusal amalgams (0-3) in all types of tissue (all P <= 0.04).
Mercury levels were significantly higher in brain tissues compared
with thyroid and kidney tissues in subjects with more than 12 occlusal
amalgam fillings (all P <= 0.01) but not in subjects with 3 or
less occlusal amalgams (all P >= 0.07).
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Latest Research Linking
Mercury To Autism
B.E. Haley/Medical Veritas 2 (2005)
Mercury toxicity: Genetic susceptibility and synergistic effects
Boyd E. Haley, PhD
Professor and Chair Department of Chemistry University of Kentucky
Abstract
Mercury toxicity and intoxication (poisoning) are realities that
every American needs to face. Both the Environmental Protection
Agency and National Academy of Science state that between 8 to 10%
of American women have mercury levels that would render any child
they gave birth to neurological disorders. One of six children in
the USA have a neurodevelopmental disorder according to the Centers
for Disease Control and Prevention. Yet our dentistry and medicine
continue to expose all patients to mercury. This article discusses
the obvious sources of mercury exposures that can be easily prevented.
It also points out that genetic susceptibility and exposures to
other materials that synergistically enhance mercury and ethyl-mercury
toxicity need to be evaluated, and that by their existence prevent
the actual determination of a "safe level" of mercury
exposure for all. The mercury sources we consider are from dentistry
and from drugs, mainly vaccines, that, in today's world are not
only unnecessary sources, but also sources that are being increasingly
recognized as being significantly deleterious to the health of many.
From the Conlusion:
... If certain infants are more susceptible to mercury toxicity
due to their inability to excrete mercury then it seems plausible
that, since this is a genetic susceptibility, older individuals
may suf fer from the inability to excrete mercury also. Based on
the ability of mercury to mimic many of the biochemical aber rancies
found in AD brain and to produce aspects of the pathological diagnostic
hallmarks of AD it seems plausible that AD is a disease related
to mercury toxicity. The published decrease of mercury in the nail
tissue of AD versus normal age-matched individuals seems to support
this possibility.
Finally, the synergistic effects of other heavy metals, diet, antibiotics,
etc. on mercury toxicity make it impossible to define a "safe
level of mercury exposure." Therefore it is imperative that
we try to eliminate all exposure to mercury; and removal from dentistry
and medicines is most important and critical for human health.
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Critical Research
Abstract
Iatrogenic Exposure
to Mercury After Hepatitis B Vaccination in Preterm Infants.
Stajichi GV; Lopex, GP; Harry, SE;
Sexson, WR.
J Pediatr., 136(5):679?8 1, May 2000.
ABSTRACT: Thimerosal, a derivative of mercury, is used as a preservative
in hepatitis B vaccines. We measured total mercury levels before
and after the administration of this vaccine in 15 preterm and 5
term infants. Comparison of pre- and post- vaccination mercury levels
showed a significant increase in both preterm and term infants after
vaccination.
Additionally, post-vaccination mercury levels were significantly
higher in preterm infants as compared with term infants. Because
mercury is known to be a potential neurotoxin to infants, further
study of its pharmaco dynamics is warranted.
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