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A margin-of-exposure approach to assessment of noncancer risks of dioxins based on human exposure and response data.

机译:一种基于人的暴露和反应数据的二恶英非癌风险评估的接触限方法。

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BACKGROUND: Risk assessment of human environmental exposure to polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/PCDFs) and other dioxin-like compounds is complicated by several factors, including limitations in measuring intakes because of the low concentrations of these compounds in foods and the environment and interspecies differences in pharmacokinetics and responses. OBJECTIVES: We examined the feasibility of relying directly on human studies of exposure and potential responses to PCDD/PCDFs and related compounds in terms of measured lipid-adjusted concentrations to assess margin of exposure (MOE) in a quantitative, benchmark dose (BMD)-based framework using representative exposure and selected response data sets. METHODS: We characterize estimated central tendency and upper-bound general U.S. population lipid-adjusted concentrations of PCDD/PCDFs from the 1970s and early 2000s based on available data sets. Estimates of benchmark concentrations for three example responses of interest (induction of cytochrome P4501A2 activity, dental anomalies, and neonatal thyroid hormone alterations) were derived based on selected human studies. RESULTS: The exposure data sets indicate that current serum lipid concentrations in young adults are approximately 6- to 7-fold lower than 1970s-era concentrations. Estimated MOEs for each end point based on current serum lipid concentrations range from < 10 for neonatal thyroid hormone concentrations to > 100 for dental anomalies-approximately 6-fold greater than would have existed during the 1970s. CONCLUSIONS: Human studies of dioxin exposure and outcomes can be used in a BMD framework for quantitative assessments of MOE. Incomplete exposure characterization can complicate the use of such studies in a BMD framework.
机译:背景:人类环境暴露于多氯二苯并-对-二恶英和二苯并呋喃(PCDD / PCDFs)以及其他类二恶英类化合物的风险评估受多种因素的影响而复杂化,包括由于食物中这些化合物的浓度低而限制摄入量环境和种间在药代动力学和反应方面的差异。目的:我们根据测得的脂质调整后的浓度,直接评估了人类对PCDD / PCDFs和相关化合物的暴露以及对PCDD / PCDFs和相关化合物的潜在反应的研究,以评估定量基准剂量(BMD)中的暴露裕度(MOE),基于框架的方法,使用代表性暴露和选定的响应数据集。方法:根据可用数据集,我们对1970年代和2000年代初期估计的中心趋势和美国人群通过脂质调整的PCDD / PCDF浓度上限进行了表征。根据选定的人体研究,得出了三个感兴趣的示例性反应(诱导细胞色素P4501A2活性,牙齿异常和新生儿甲状腺激素改变)的基准浓度估算值。结果:暴露数据集表明,目前年轻人中的血脂浓度比1970年代低约6至7倍。根据当前血清脂质浓度,每个终点的估计MOE从新生儿甲状腺激素浓度的<10到牙齿异常的> 100,比1970年代的水平高出约6倍。结论:人体对二恶英暴露和结果的研究可用于BMD框架中,用于MOE的定量评估。不完全的暴露特征可能会使这种研究在BMD框架中的使用复杂化。

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