National Center for Environmental Assessment, US Environmental Protection Agency, 26 West Martin Luther King Drive, Cincinnati, OH 45268, USA.
Regul Toxicol Pharmacol. 2012 Jun;63(1):10-9. doi: 10.1016/j.yrtph.2012.02.006. Epub 2012 Feb 17.
Hazard identification and dose-response assessment for chemicals of concern found in various environmental media are typically based on epidemiological and/or animal toxicity data. However, human health risk assessments are often requested for many compounds found at contaminated sites throughout the US that have limited or no available toxicity information from either humans or animals. To address this issue, recent efforts have focused on expanding the use of structure-activity relationships (SAR) approaches to identify appropriate surrogates and/or predict toxicological phenotype(s) and associated adverse effect levels. A tiered surrogate approach (i.e., decision tree) based on three main types of surrogates (structural, metabolic, and toxicity-like) has been developed. To select the final surrogate chemical and its surrogate toxicity value(s), a weight-of-evidence approach based on the proposed decision tree is applied. In addition, a case study with actual toxicity data serves as the evaluation to support our tiered surrogate approach. Future work will include case studies demonstrating the utility of the surrogate approach under different scenarios for data-poor chemicals. In conclusion, our surrogate approach provides a reasonable starting point for identifying potential toxic effects, target organs, and/or modes-of-action, and for selecting surrogate chemicals from which to derive either reference or risk values.
危害识别和剂量-反应评估通常基于流行病学和/或动物毒性数据,用于各种环境介质中发现的关注化学物质。然而,对于美国各地污染场所中发现的许多化合物,由于人类或动物的毒性信息有限或不存在,通常需要进行人类健康风险评估。为了解决这个问题,最近的工作重点是扩大使用结构-活性关系(SAR)方法来识别合适的替代物和/或预测毒理学表型和相关的不良效应水平。已经开发了一种基于三种主要类型替代物(结构、代谢和毒性样)的分层替代物方法(即决策树)。为了选择最终的替代化学品及其替代毒性值,将应用基于拟议决策树的证据权重方法。此外,使用实际毒性数据的案例研究作为支持我们分层替代方法的评估。未来的工作将包括展示在不同数据匮乏化学品情况下替代方法的实用性的案例研究。总之,我们的替代方法为识别潜在的毒性效应、靶器官和/或作用模式以及从替代化学品中选择推导参考或风险值提供了合理的起点。