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Dispelling urban myths about default uncertainty factors in chemical risk assessment – sufficient protection against mixture effects?

机译:消除关于化学品风险评估中默认不确定性因素的城市神话–足够的保护以防混合物影响?

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摘要

Assessing the detrimental health effects of chemicals requires the extrapolation of experimental data in animals to human populations. This is achieved by applying a default uncertainty factor of 100 to doses not found to be associated with observable effects in laboratory animals. It is commonly assumed that the toxicokinetic and toxicodynamic sub-components of this default uncertainty factor represent worst-case scenarios and that the multiplication of those components yields conservative estimates of safe levels for humans. It is sometimes claimed that this conservatism also offers adequate protection from mixture effects. By analysing the evolution of uncertainty factors from a historical perspective, we expose that the default factor and its sub-components are intended to represent adequate rather than worst-case scenarios. The intention of using assessment factors for mixture effects was abandoned thirty years ago. It is also often ignored that the conservatism (or otherwise) of uncertainty factors can only be considered in relation to a defined level of protection. A protection equivalent to an effect magnitude of 0.001-0.0001% over background incidence is generally considered acceptable. However, it is impossible to say whether this level of protection is in fact realised with the tolerable doses that are derived by employing uncertainty factors. Accordingly, it is difficult to assess whether uncertainty factors overestimate or underestimate the sensitivity differences in human populations. It is also often not appreciated that the outcome of probabilistic approaches to the multiplication of sub-factors is dependent on the choice of probability distributions. Therefore, the idea that default uncertainty factors are overly conservative worst-case scenarios which can account both for the lack of statistical power in animal experiments and protect against potential mixture effects is ill-founded. We contend that precautionary regulation should provide an incentive to generate better data and recommend adopting a pragmatic, but scientifically better founded approach to mixture risk assessment.
机译:评估化学品的有害健康影响需要将动物实验数据推算给人类。这是通过将默认不确定性因子100应用于未发现与实验动物中可观察到的效应相关的剂量来实现的。通常假定此默认不确定性因素的毒物动力学和毒物动力学子组件代表最坏的情况,并且将这些组件相乘得出对人类安全水平的保守估计。有时有人声称这种保守性还提供了充分的保护,以防止混合效应。通过从历史的角度分析不确定性因素的演变,我们发现默认因素及其子组件旨在代表适当的情况,而不是最坏的情况。 30年前就放弃了使用评估因子来实现混合效果的意图。人们通常也忽略了不确定因素的保守性(或其他方式)只能与已定义的保护级别有关。通常认为与背景发生率等效的影响幅度为0.001-0.0001%的保护是可以接受的。但是,无法说出这种保护水平是否实际上是通过采用不确定因素得出的可耐受剂量实现的。因此,难以评估不确定性因素是高估还是低估了人口中的敏感性差异。人们通常也不认识到,采用概率方法处理子因子的结果取决于概率分布的选择。因此,默认不确定性因素是过于保守的最坏情况,这种想法既可以解释动物实验中缺乏统计能力,又可以防止潜在的混合效应,这一观点是没有根据的。我们认为,预防性法规应激励人们产生更好的数据,并建议采用务实但科学上更完善的方法进行混合风险评估。

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