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revised final - Agency for Toxic Substances and Disease Registry ...

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MERCURY 311<br />

2. HEALTH EFFECTS<br />

to hazardous substances that are commonly found in body tissues <strong>and</strong> fluids (essential mineral nutrients [e.g.,<br />

copper, zinc, <strong>and</strong> selenium]). Biomarkers of exposure to mercury are discussed in Section 2.7.1.<br />

Biomarkers of effect are defined as any measurable biochemical, physiological, or other alteration within an<br />

organism that, depending on magnitude, can be recognized as an established or potential health impairment<br />

or disease (NAS/NRC 1989). This definition encompasses biochemical or cellular signals of tissue<br />

dysfunction (e.g., increased liver enzyme activity or pathological changes in female genital epithelial cells),<br />

as well as physiological signs of dysfunction such as increased blood pressure or decreased lung capacity.<br />

Note that these markers are not often substance specific. They also may not be directly adverse, but they can<br />

indicate potential health impairment (e.g., DNA adducts). Biomarkers of effect caused by mercury are<br />

discussed in Section 2.7.2.<br />

A biomarker of susceptibility is an indicator of an inherent or acquired limitation of an organism's ability to<br />

respond to the challenge of exposure to a specific xenobiotic substance. It can be an intrinsic genetic or<br />

other characteristic or a pre-existing disease that results in an increase in the absorbed dose, a decrease in the<br />

biologically effective dose, or a target tissue response. If biomarkers of susceptibility exist, they are<br />

discussed in Section 2.8 (Populations That Are Unusually Susceptible).<br />

2.7.1 Biomarkers Used to Identify or Quantify Exposure to Mercury<br />

Blood <strong>and</strong> urine mercury concentrations are commonly used as biomarkers of exposure to mercury. Hair has<br />

been used as a biomarker of exposure to methylmercury. Occupational studies show that recent mercury<br />

exposure is reflected in blood <strong>and</strong> urine (Naleway et al. 1991; WHO 1991). However, at low exposure levels<br />

(

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