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Incorporating Regulatory Guideline Values in Analysis of Epidemiology Data

机译:在分析流行病学数据分析中纳入监管指南值

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Fundamental to regulatory guidelines is to identify chemicals that are implicated with adverse human health effects and inform public health risk assessors about "acceptable ranges" of such environmental exposures (e.g., from consumer products and pesticides). The process is made more difficult when accounting for complex human exposures to multiple environmental chemicals. Herein we propose a new class of nonlinear statistical models for human data that incorporate and evaluate regulatory guideline values into analyses of health effects of exposure to chemical mixtures using so-called 'desirability functions' (DFs). The DFs are incorporated into nonlinear regression models to allow for the simultaneous estimation of points of departure for risk assessment of combinations of individual substances that are parts of chemical mixtures detected in humans. These are, in contrast to published so-called biomonitoring equivalent (BE) values and human biomonitoring (HBM) values that link regulatory guideline values from in vivo studies of single chemicals to internal concentrations monitored in humans. We illustrate the strategy through the analysis of prenatal concentrations of mixtures of 11 chemicals and two health effects: birth weight and language delay at 2.5 years. The strategy allows for the creation of a Mixture DF, which is a uni-dimensional construct of single chemical DFs, which focuses the resulting inference to a single dimension for a more powerful one degree-of-freedom test of significance. Based on the application of this new method we conclude that the guideline values need to be lower than those for single chemicals when observed in combination to achieve a similar level of protection as was aimed for the individual chemicals. The proposed modeling may thus suggest data-driven uncertainty factors for single chemical risk assessment that takes environmental mixtures into account. (Support: NIH #R01ES028811 and EU Horizon 2020 #634880)
机译:监管指南的基础是鉴定与不良人体健康影响有关的化学品,并通知公共卫生风险评估员关于这种环境暴露的“可接受范围”(例如,来自消费产品和杀虫剂)。当核算复杂的人体暴露于多种环境化学品时,该过程变得更加困难。在此,我们向人类数据提出了一种新的非线性统计模型,该数据纳入并评估了使用所谓的“可归函数”(DFS)暴露于化学混合物的健康效果的分析。 DF被纳入非线性回归模型,以允许同时估计风险评估的风险评估,这是人类中检测到的化学混合物的一部分。相反,与公开的所谓的生物监测等效物(BE)值和人生物监测值(HBM)值与单一化学物质的体内研究链接到人类中监测的内部浓度。我们通过分析11种化学物质和两种健康影响的产前浓度的产前浓度:25岁时出生体重和语言延迟来说明该策略。该策略允许创建混合DF,其是单维化学DFS的一维构建,其将所得引起的引人注于单个维度,以获得更强大的一种自由度的重要性测试。基于这种新方法的应用,我们得出结论,准则值需要低于单一化学品的指南,以便组合观察到实现类似的保护水平,因为旨在为单独的化学物质而言。因此,所提出的建模可以提出数据驱动的不确定性因素,以考虑到环境混合物的单一化学风险评估。 (支持:nih#r01es028811和欧盟地平线2020#634880)

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