US Army Engineer Research and Development Center, Vicksburg, MS, USA.
Department of Chemical Engineering, National Institute of Technology Agartala, Barjala, Jirania, West Tripura, Tripura, India.
ALTEX. 2019;36(1):91-102. doi: 10.14573/altex.1808241. Epub 2018 Oct 16.
Current efforts in chemical safety are focused on utilizing human in vitro or alternative animal data in biological pathway context. However, it remains unclear how biological pathways, and toxicology data developed in that context, can be used to quantitatively facilitate decision-making. The objective of this work is to determine if hypothesis testing using Adverse Outcome Pathways (AOPs) can provide quantitative chemical hazard predictions. Current methods for predicting hazards of chemicals in a biological pathway context were extensively reviewed, specific case studies examined and computational modeling used to demonstrate quantitative hazard prediction based on an AOP. Since AOPs are chemically agnostic, we propose that AOPs function as hypotheses for how specific chemicals may cause adverse effects via specific pathways. Three broad approaches were identified for testing the hypothesis with AOPs, semi-quantitative weight of evidence, probabilistic, and mechanistic modeling. We then demonstrate how these approaches could be used to test hypotheses using high throughput in vitro data and alternative animal data. Finally, we discuss standards in development and documentation that would facilitate use in a regulatory context. We conclude that quantitative AOPs provide a flexible hypothesis framework for predicting chemical hazards. It accommodates a wide range of approaches that are useful at many stages and build upon one another to become increasingly quantitative.
目前,化学安全方面的工作重点是利用人类体外或替代动物数据来构建生物学途径。然而,目前尚不清楚如何利用生物学途径以及在该背景下开发的毒理学数据来进行定量决策。本研究旨在确定是否可以使用不良结局途径(AOP)进行假设检验,以提供定量的化学危害预测。本研究广泛回顾了目前用于预测生物途径中化学物质危害的方法,研究了具体案例,并使用计算模型来证明基于 AOP 的定量危害预测。由于 AOP 与化学物质无关,我们提出 AOP 可作为特定化学物质通过特定途径引起不良反应的假设。确定了三种广泛的方法来通过 AOP 检验假设,即半定量证据权重、概率和机制建模。然后,我们展示了如何使用高通量体外数据和替代动物数据来测试这些假设。最后,我们讨论了正在制定的标准和文件,这将有助于在监管环境中使用。我们得出结论,定量 AOP 为预测化学危害提供了一个灵活的假设框架。它可以容纳各种在许多阶段都很有用的方法,并相互构建,变得越来越定量。