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A new method for generating distributions of biomonitoring equivalents to support exposure assessment and prioritization

机译:一种新方法,用于产生生物监唱等同物的分布,以支持暴露评估和优先级

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Biomonitoring data are now available for hundreds of chemicals through state and national health surveys. Exposure guidance values also exist for many of these chemicals. Several methods are frequently used to evaluate biomarker data with respect to a guidance value. The "biomonitoring equivalent" (BE) approach estimates a single biomarker concentration (called the BE) that corresponds to a guidance value (e.g., Maximum Contaminant Level, Reference Dose, etc.), which can then be compared with measured biomarker data. The resulting "hazard quotient" estimates (HQ = biomarker concentration/BE) can then be used to prioritize chemicals for follow-up examinations. This approach is used exclusively for population-level assessments, and works best when the central tendency of measurement data is considered. Complementary approaches are therefore needed for assessing individual biomarker levels, particularly those that fall within the upper percentiles of measurement distributions. In this case study, probabilistic models were first used to generate distributions of BEs for perchlorate based on the point-of-departure (POD) of 7. μg/kg/day. These distributions reflect possible biomarker concentrations in a hypothetical population where all individuals are exposed at the POD. A statistical analysis was then performed to evaluate urinary perchlorate measurements from adults in the 2001 to 2002 National Health and Nutrition Examination Survey (NHANES). Each NHANES adult was assumed to have experienced repeated exposure at the POD, and their biomarker concentration was interpreted probabilistically with respect to a BE distribution. The HQ based on the geometric mean (GM) urinary perchlorate concentration was estimated to be much lower than unity (HQ. ≈. 0.07). This result suggests that the average NHANES adult was exposed to perchlorate at a level well below the POD. Regarding individuals, at least a 99.8% probability was calculated for all but two NHANES adults that a higher biomarker concentration would have been observed compared to what was actually measured if the daily dietary exposure had been at the POD. This is strong evidence that individual perchlorate exposures in the 2001-2002 NHANES adult population were likely well below the POD. This case study demonstrates that the "stochastic BE approach" provides useful quantitative metrics, in addition to HQ estimates, for comparison across chemicals. This methodology should be considered when evaluating biomarker measurements against exposure guidance values, and when examining chemicals that have been identified as needing follow-up investigation based on existing HQ estimates.
机译:现在可以通过国家和国家健康调查获得数百种化学品的生物监测数据。对于许多这些化学品也存在曝光引导值。经常用于评估关于引导值的生物标志物数据的几种方法。 “生物监测当量”(BE)方法估计与指导值(例如,最大污染物水平,参考剂量等)对应的单一生物标志物浓度(称为BE),然后可以将其与测量的生物标志物数据进行比较。然后可以使用所得到的“危害商”估计(HQ =生物标志物浓度/是),以优先考虑化学品以进行后续检查。这种方法专门用于人口级评估,当考虑测量数据的中心趋势时,最佳工作。因此,需要补充方法来评估个体生物标志物水平,特别是那些落在测量分布的上百分百分比内的方法。在这种情况下,首先使用概率模型基于7.μg/ kg /天的偏离点(pod)产生高氯酸盐的分布。这些分布反映了在假设群体中可能的生物标志物浓度,其中所有个体在豆荚处暴露。然后进行统计分析以评估2001年至2002年全国卫生和营养考试调查(NHANES)的成人的尿酸尿含量。每个NHANES成人被认为在豆荚处经历了反复暴露,并且它们的生物标志物浓度相对于分布被解释了概率。估计基于几何平均值(GM)尿状氯酸盐浓度的HQ远低于Unity(HQ.0.07)。该结果表明,将平均NHANES成人暴露于豆荚下方的水平下的高氯酸盐。关于个体,除了每日膳食暴露于豆荚的实际测量时,所有除了两种NHANES成年人的所有耐药物浓度都将遵守较高的生物标志物浓度,至少计算99.8%的概率。这是强有力的证据表明,2001 - 2002年纳汉斯成年人人口中的全氯酸盐暴露可能很远低于豆荚。这种情况研究表明,除了总HQ估计之外,“随机是方法”提供有用的定量度量,以进行化学品。当评估曝光引导值的生物标志物测量时,以及在检查所确定的化学物质时,应考虑这种方法,以及根据现有的总HQ估计所需进行后续调查。

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