U.S. Environmental Protection Agency, Office of Research and Development, National Health and Environmental Effects Research Laboratory , Research Triangle Park, North Carolina 27709, United States.
U.S. Environmental Protection Agency, Office of Research and Development, National Center for Environmental Assessment , Research Triangle Park, North Carolina 27709, United States.
Environ Sci Technol. 2018 Jan 16;52(2):839-849. doi: 10.1021/acs.est.7b04940. Epub 2017 Dec 29.
Cumulative risk assessment (CRA) methods promote the use of a conceptual site model (CSM) to apportion exposures and integrate risk from multiple stressors. While CSMs may encompass multiple species, evaluating end points across taxa can be challenging due to data availability and physiological differences among organisms. Adverse outcome pathways (AOPs) describe biological mechanisms leading to adverse outcomes (AOs) by assembling causal pathways with measurable intermediate steps termed key events (KEs), thereby providing a framework for integrating data across species. In this work, we used a case study focused on the perchlorate anion (ClO) to highlight the value of the AOP framework for cross-species data integration. Computational models and dose-response data were used to evaluate the effects of ClO in 12 species and revealed a dose-response concordance across KEs and taxa. The aggregate exposure pathway (AEP) tracks stressors from sources to the exposures and serves as a complement to the AOP. We discuss how the combined AEP-AOP construct helps to maximize the use of existing data and advances CRA by (1) organizing toxicity and exposure data, (2) providing a mechanistic framework of KEs for integrating data across human health and ecological end points, (3) facilitating cross-species dose-response evaluation, and (4) highlighting data gaps and technical limitations.
累积风险评估 (CRA) 方法促进了概念场地模型 (CSM) 的使用,以分配暴露量并整合来自多种胁迫因素的风险。虽然 CSM 可能包含多个物种,但由于数据可用性和生物体之间的生理差异,评估跨分类群的终点可能具有挑战性。 不良结局途径 (AOP) 通过将具有可测量中间步骤(称为关键事件 (KEs) 的因果途径组装在一起,描述导致不良结局 (AOs) 的生物学机制,从而为跨物种数据集成提供了框架。在这项工作中,我们使用了一个以高氯酸盐阴离子 (ClO) 为重点的案例研究,突出了 AOP 框架在跨物种数据集成中的价值。 计算模型和剂量-反应数据用于评估 12 个物种中 ClO 的影响,并揭示了 KEs 和分类群之间的剂量-反应一致性。 综合暴露途径 (AEP) 跟踪从源到暴露的胁迫因素,是 AOP 的补充。 我们讨论了如何通过以下方式来帮助最大程度地利用现有数据并推进 CRA:(1)组织毒性和暴露数据,(2)为整合人类健康和生态终点的 KEs 提供机制框架,(3)促进跨物种剂量-反应评估,以及(4)突出数据差距和技术限制。