Spînu Nicoleta, Cronin Mark T D, Lao Junpeng, Bal-Price Anna, Campia Ivana, Enoch Steven J, Madden Judith C, Mora Lagares Liadys, Novič Marjana, Pamies David, Scholz Stefan, Villeneuve Daniel L, Worth Andrew P
School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Byrom Street, Liverpool L3 3AF, UK.
Department of Psychology, University of Fribourg, Fribourg CH-1700, Switzerland.
Comput Toxicol. 2022 Feb;21:100206. doi: 10.1016/j.comtox.2021.100206.
In a century where toxicology and chemical risk assessment are embracing alternative methods to animal testing, there is an opportunity to understand the causal factors of neurodevelopmental disorders such as learning and memory disabilities in children, as a foundation to predict adverse effects. New testing paradigms, along with the advances in probabilistic modelling, can help with the formulation of mechanistically-driven hypotheses on how exposure to environmental chemicals could potentially lead to developmental neurotoxicity (DNT). This investigation aimed to develop a Bayesian hierarchical model of a simplified AOP network for DNT. The model predicted the probability that a compound induces each of three selected common key events (CKEs) of the simplified AOP network and the adverse outcome (AO) of DNT, taking into account correlations and causal relations informed by the key event relationships (KERs). A dataset of 88 compounds representing pharmaceuticals, industrial chemicals and pesticides was compiled including physicochemical properties as well as and information. The Bayesian model was able to predict DNT potential with an accuracy of 76%, classifying the compounds into low, medium or high probability classes. The modelling workflow achieved three further goals: it dealt with missing values; accommodated unbalanced and correlated data; and followed the structure of a directed acyclic graph (DAG) to simulate the simplified AOP network. Overall, the model demonstrated the utility of Bayesian hierarchical modelling for the development of quantitative AOP (qAOP) models and for informing the use of new approach methodologies (NAMs) in chemical risk assessment.
在一个毒理学和化学风险评估正在采用替代动物试验方法的世纪里,有机会了解儿童神经发育障碍(如学习和记忆障碍)的因果因素,作为预测不良反应的基础。新的测试范式,以及概率建模的进展,有助于形成关于接触环境化学物质如何可能导致发育性神经毒性(DNT)的机制驱动假说。本研究旨在开发一个用于DNT的简化不良结局途径(AOP)网络的贝叶斯层次模型。该模型预测了一种化合物诱导简化AOP网络的三个选定常见关键事件(CKEs)以及DNT不良结局(AO)的概率,同时考虑了关键事件关系(KERs)所提供的相关性和因果关系。编制了一个包含88种化合物的数据集,这些化合物代表药品、工业化学品和农药,包括物理化学性质以及相关信息。贝叶斯模型能够以76%的准确率预测DNT潜力,将化合物分为低、中或高概率类别。建模工作流程还实现了另外三个目标:处理缺失值;处理不平衡和相关数据;并遵循有向无环图(DAG)的结构来模拟简化的AOP网络。总体而言,该模型证明了贝叶斯层次建模在开发定量AOP(qAOP)模型以及为化学风险评估中使用新方法学(NAMs)提供信息方面的实用性。