4.4 Article

Biomonitoring Equivalents for molybdenum

Journal

REGULATORY TOXICOLOGY AND PHARMACOLOGY
Volume 77, Issue -, Pages 223-229

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.yrtph.2016.03.004

Keywords

Biomonitoring; Biomonitoring; Equivalents; Molybdenum; Risk assessment

Funding

  1. Health Canada [4500323309]

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Molybdenum is an essential trace element for mammalian, plant, and other animal systems. The Institute of Medicine (IOM) has established an Estimated Average Requirement (EAR) to assure sufficient molybdenum intakes for human populations; however excessive exposures can cause toxicity. As a result, several agencies have established exposure guidance values to protect against molybdenum toxicity, including a Reference Dose (RfD), Tolerable Daily Intake (TDI) and a Tolerable Upper Intake Level (UL). Biomonitoring for molybdenum in blood or urine in the general population is being conducted by the Canadian Health Measures Survey (CHMS) and the U.S. National Health and Nutrition Examination Survey (NHANES). Using pharmacokinetic data from controlled human dosing studies, Biomonitoring Equivalents (BEs) were calculated for molybdenum in plasma, whole blood, and urine associated with exposure guidance values set to protect against both nutritional deficits and toxicity. The BEEAR values in plasma, whole blood and urine are 0.5, 0.45 and 22 mu g/L, respectively. The BEs associated with toxicity range from 0.9 to 31 mu g/L in plasma, 0.8-28 mu g/L in whole blood and 200-7500 mu g/L in urine. These values can be used to interpret molybdenum biomonitoring data from a nutritional and toxicity perspective. (C) 2016 Published by Elsevier Inc.

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