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MERCURY 322<br />

2. HEALTH EFFECTS<br />

mercury was expressed by the equation 10 log (acceleration)=G0.888 + 0.0059 (urine mercury) (r=0.39,<br />

p50 µg/g creatinine can cause a dose-related loss of color vision.<br />

An association between urine mercury levels <strong>and</strong> per<strong>for</strong>mance on memory tests <strong>and</strong> verbal intelligence<br />

tests has been established. Abnormal results on memory tests were reported <strong>for</strong> 9 workers exposed to<br />

mercury in the production of thermometers; urinary mercury excretion levels were 7–1,101 µg/24 hours<br />

(Vroom <strong>and</strong> Greer 1972). The short-term memory span of 26 workers was examined by Smith et al.<br />

(1983) <strong>and</strong> found to decrease with increasing urine mercury levels. The range of mercury found in the<br />

urine of these workers was 0–510 µg/L. A significant linear relationship was reported between subjects'<br />

50% memory threshold spans <strong>and</strong> 12-month urinary mercury concentrations. Disturbances on tests of<br />

verbal intelligence <strong>and</strong> memory were more frequent among individuals with mercury blood levels above<br />

1.5 µg/100 mL <strong>and</strong> mercury urine levels above 56 µg/L in 36 male chloralkali workers (Piikivi et al.<br />

1984).<br />

Potential biomarkers <strong>for</strong> the autoimmune effects of mercury include measurement of antiglomerular<br />

basement membrane antibodies, anti-DNA antibodies, serum IgE complexes, <strong>and</strong> total IgE (Cardenas et al.<br />

1993). Elevated IgE, antiglomerular basement membrane antibodies, <strong>and</strong> anti-DNA antibodies have been<br />

observed in a few persons with exposure to mercury from dental amalgams (Anneroth et al. 1992). Other<br />

individuals have also been shown to have elevated anti-DNA or antiglomerular basement membrane<br />

antibodies (Cardenas et al. 1993; Langworth et al. 1992b).<br />

Recent data regarding the action of low-level mercury exposure on receptors <strong>and</strong> signal transduction<br />

pathways in peripheral lymphocytes suggest potential applications of certain surrogate markers in<br />

mechanistic studies of neurotoxicity <strong>and</strong>, possibly, in assessing early biochemical effects of neurotoxicants<br />

in humans (Manzo et al. 1995). Additional biomarkers <strong>for</strong> effects on the immune, renal, hepatic, <strong>and</strong><br />

neurological systems are presented in the CDC/ATSDR (1990) <strong>and</strong> OTA (1990) reports. See Section 2.2<br />

<strong>for</strong> a more detailed discussion of the effects caused by mercury.

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