Lack of significant risk from everyday dietary nickel: Rethinking the application of oral toxicity reference values

IF 4.3 4区 医学 Q1 MEDICINE, LEGAL
Regulatory Toxicology and Pharmacology Pub Date : 2026-05-01 Epub Date: 2026-02-09 DOI:10.1016/j.yrtph.2026.106055
Michael D. Dutton , Chris Bacigalupo
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引用次数: 0

Abstract

Toxicity reference value (TRV) is a general term for an exposure limit below which health impairment is not expected. TRVs are used to develop environmental quality standards and for other risk-based activities. Nickel (Ni) TRVs developed by several influential regulatory agencies have used toxicity data from rats orally exposed to nickel sulfate hexahydrate (NSHH). These TRVs converted doses from an NSHH-basis to an ‘as-nickel’ basis, under the belief that controls received no Ni, which is not the case. The extrapolation from a point-of-departure to a human-relevant limit has resulted in TRVs that are, in some instances, less than the estimated normal daily dietary nickel intake observed in certain human life stages. As a result, Ni that is present naturally in food has been incorrectly believed to be contributing to human health risk. The now common risk assessment practice of applying these Ni TRVs on an ‘inclusive of baseline diet’ basis, contrasts with the Institute of Medicine (IOM) perspective that there is no evidence of adverse effects associated with a normal diet: rather, human health risk is associated with excess nickel intake as soluble nickel salts. TRVs based on soluble Ni salts are to be distinguished from the normal Ni-containing diet.
每日膳食镍缺乏显著风险:重新思考口服毒性参考值的应用。
毒性参考值(TRV)是暴露限值的总称,低于该限值预计不会对健康造成损害。trv用于制定环境质量标准和其他基于风险的活动。由几个有影响力的监管机构开发的镍(Ni) TRVs使用了大鼠口服暴露于六水合硫酸镍(NSHH)的毒性数据。这些trv将剂量从以nsh为基础转换为以“镍”为基础,认为对照者没有接受镍,但事实并非如此。从起点到与人类有关的限度的外推导致在某些情况下,trv低于在某些人类生命阶段观察到的正常每日饮食镍摄入量的估计。因此,人们错误地认为食物中天然存在的镍会对人类健康造成威胁。目前普遍的风险评估做法是在“包括基线饮食”的基础上应用这些镍trv,这与医学研究所(IOM)的观点形成对比,即没有证据表明与正常饮食相关的不利影响:相反,人类健康风险与作为可溶性镍盐摄入过量的镍有关。以可溶性镍盐为基础的trv应与普通含镍日粮区别开来。
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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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