Toxicity reference values (TRVs) for force health protection: Gap identification and TRV prediction

IF 3 4区 医学 Q1 MEDICINE, LEGAL
Lisa M. Sweeney , Teresa R. Sterner
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Abstract

The mission of the Force Health Protection (FHP) program of the U.S. Air Force (USAF), sustaining the readiness of warfighters, relies on determinations of acceptable levels of exposure to a wide array of substances that USAF personnel may encounter. In many cases, exposure details are limited or authoritative toxicity reference values (TRVs) are unavailable. To address some of the TRV gaps, we are integrating several approaches to generate health protective exposure guidelines. Descriptions are provided for identification of chemicals of interest for USAF FHP (467 to date), synthesis of multiple TRVs to derive Operational Exposure Limits (OpELs), and strategies for identifying and developing candidate values for provisional OpELs when authoritative TRVs are lacking. Rodent bioassay-derived long-term Derived No Effect Levels (DNELs) for workers were available only for a minority of the substances with occupational TRV gaps (19 of 84). Additional occupational TRV estimation approaches were found to be straightforward to implement: Tier 1 Occupational Exposure Bands, cheminformatics approaches (multiple linear regression and novel nearest-neighbor approaches), and empirical adjustment of short term TRVs. Risk assessors working in similar contexts may benefit from application of the resources referenced and developed in this work.

Abstract Image

保护部队健康的毒性参考值 (TRV):差距识别和 TRV 预测。
美国空军(USAF)部队健康保护(FHP)计划的任务是维持作战人员的战备状态,这依赖于对美国空军人员可能接触到的各种物质的可接受接触水平的确定。在许多情况下,暴露详情有限,或者没有权威的毒性参考值 (TRV)。为了填补 TRV 方面的一些空白,我们正在整合多种方法,以生成保护健康的暴露指南。本文介绍了如何确定美国空军 FHP 所关注的化学物质(迄今已有 467 种)、如何综合多个 TRV 值以得出操作接触限值 (OpEL),以及如何在缺乏权威 TRV 值的情况下确定和开发临时 OpEL 的候选值。只有少数存在职业 TRV 缺口的物质(84 种物质中的 19 种)可以通过啮齿动物生物测定得出工人的长期衍生无效应水平 (DNEL)。其他职业 TRV 估算方法被认为可以直接实施:第 1 级职业接触带、化学信息学方法(多元线性回归和新型近邻方法)以及短期 TRV 的经验调整。在类似情况下工作的风险评估人员可能会从应用这项工作中参考和开发的资源中受益。
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来源期刊
CiteScore
6.70
自引率
8.80%
发文量
147
审稿时长
58 days
期刊介绍: Regulatory Toxicology and Pharmacology publishes peer reviewed articles that involve the generation, evaluation, and interpretation of experimental animal and human data that are of direct importance and relevance for regulatory authorities with respect to toxicological and pharmacological regulations in society. All peer-reviewed articles that are published should be devoted to improve the protection of human health and environment. Reviews and discussions are welcomed that address legal and/or regulatory decisions with respect to risk assessment and management of toxicological and pharmacological compounds on a scientific basis. It addresses an international readership of scientists, risk assessors and managers, and other professionals active in the field of human and environmental health. Types of peer-reviewed articles published: -Original research articles of relevance for regulatory aspects covering aspects including, but not limited to: 1.Factors influencing human sensitivity 2.Exposure science related to risk assessment 3.Alternative toxicological test methods 4.Frameworks for evaluation and integration of data in regulatory evaluations 5.Harmonization across regulatory agencies 6.Read-across methods and evaluations -Contemporary Reviews on policy related Research issues -Letters to the Editor -Guest Editorials (by Invitation)
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