Center for Public Health and Environmental Assessment (CPHEA), Mail code 8623R, USA; United States (US) Environmental Protection Agency, Washington, DC 20460, USA.
Office of Children's Health Protection (OCHP), Mail code 1107T, USA; United States (US) Environmental Protection Agency, Washington, DC 20460, USA.
Environ Int. 2020 Jan;134:105287. doi: 10.1016/j.envint.2019.105287. Epub 2019 Nov 26.
The phthalate syndrome (PS) is a collection of related male reproductive developmental effects, ranging in severity, that have been observed in rats after gestational exposure to developmentally-toxic phthalates. For statistical purposes, the PS is defined as a single endpoint and one dose-response analysis is conducted, rather than conducting multiple analyses on each individual endpoint.
To improve dose-response modeling approaches for the PS and other syndromes of effects by accounting for differing severity levels among the endpoints.
Ordinal dose-response modeling was performed on PS data from a published study of diisobutyl phthalate (DIBP) gestational exposure to male Sprague-Dawley rats. To incorporate PS endpoint severity, the endpoints were categorized into ordinal levels based on the expected impact of male developmental endpoint's on fertility. Then, a benchmark dose was estimated for each ordinal level. A bootstrap procedure was used to account for the nested nature of the data, and a sensitivity analysis was performed to assess the bootstrap results. A comparison of the estimates between the ordinal and the dichotomous model was performed.
The ordinal version of the log-logistic model applied to the data categorized by PS endpoint severity level provided benchmark dose estimates that were closer to each other in value and had lower variability than the traditional dichotomous application. The sensitivity analysis confirmed the validity of the bootstrap results.
The ordinal dose-response modeling method accounts for severity differences among dichotomous PS endpoints, can be expanded in the future to include more severity levels, and can be used in both single and cumulative phthalate risk assessments.
邻苯二甲酸酯综合征(PS)是一系列相关的雄性生殖发育效应的集合,在妊娠接触发育毒性邻苯二甲酸酯的大鼠中观察到严重程度不同的效应。出于统计目的,PS 被定义为单一终点,进行单一剂量反应分析,而不是对每个单独的终点进行多次分析。
通过考虑终点之间的严重程度差异,改进 PS 和其他效应综合征的剂量反应建模方法。
对已发表的邻苯二甲酸二异丁酯(DIBP)妊娠暴露雄性 Sprague-Dawley 大鼠 PS 数据进行有序剂量反应建模。为了纳入 PS 终点严重程度,根据雄性发育终点对生育能力的预期影响,将终点分为有序水平。然后,为每个有序水平估计基准剂量。使用自举程序来解释数据的嵌套性质,并进行敏感性分析以评估自举结果。比较有序和二项式模型之间的估计值。
应用于按 PS 终点严重程度分类的数据的有序对数逻辑模型提供了基准剂量估计值,它们在数值上彼此更接近,并且比传统的二项式应用具有更低的变异性。敏感性分析证实了自举结果的有效性。
有序剂量反应建模方法考虑了二项式 PS 终点之间的严重程度差异,可以在未来扩展到包括更多的严重程度水平,并可用于单一和累积邻苯二甲酸酯风险评估。