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时变暴露对有毒物质反应的影响。

Effects of time-variant exposure on toxic substance response.

作者信息

Morrison P F

机构信息

Biomedical Engineering and Instrumentation Branch, National Institutes of Health, Bethesda, MD 20892.

出版信息

Environ Health Perspect. 1987 Dec;76:133-9. doi: 10.1289/ehp.8776133.

Abstract

Sources of time-variant exposure to toxic substances are identified and examined for their effects on the estimation of response. It is shown that only time-averaged target tissue concentrations are required to obtain rigorous risk estimates from the one-hit and multihit models. In contrast, detailed concentration histories need to be retained throughout analyses involving two-event models with intermediate-stage clonal growth advantage (clonal two-stage) and multistage models. Cumulative incidence ratios, based on the exact to time-averaged treatment of concentration time dependencies, are evaluated for substances whose toxic responses exhibit moderate (arsenic) and strong (ethylene dibromide) dependence on time of actual exposure. These ratios reveal that time-averaged dose approximations may lead to several orders of magnitude error in both the multistage and clonal two-stage models if exposure periods are short, and that 3.4-fold (arsenic) and 8-fold (ethylene dibromide) errors still exist even when an actual two-thirds lifetime exposure is averaged over a full lifetime. Finally, the effects of time-variant exposure on risk estimation due to migration and birth-death in an epidemiological setting are examined. A residence time distribution calculation shows that, if these effects are ignored for a population orally exposed to arsenic and characterized by an out-migration rate in excess of 5%/yr, response errors will exceed an order of magnitude.

摘要

识别并研究了随时间变化的有毒物质暴露源及其对反应估计的影响。结果表明,从单击中模型和多击中模型获得严格的风险估计仅需要时间平均的靶组织浓度。相比之下,在涉及具有中间阶段克隆生长优势的两事件模型(克隆两阶段)和多阶段模型的整个分析过程中,需要保留详细的浓度历史。对于其毒性反应对实际暴露时间呈现中度(砷)和强烈(二溴乙烷)依赖性的物质,基于对浓度时间依赖性的精确到时间平均处理来评估累积发病率比。这些比率表明,如果暴露期较短,在多阶段模型和克隆两阶段模型中,时间平均剂量近似可能导致几个数量级的误差,并且即使将实际三分之二寿命暴露在整个寿命期间进行平均,仍然存在3.4倍(砷)和8倍(二溴乙烷)的误差。最后,研究了在流行病学环境中由于迁移和出生 - 死亡导致的随时间变化的暴露对风险估计的影响。停留时间分布计算表明,如果对于口服暴露于砷且以每年超过5%的迁出率为特征的人群忽略这些影响,反应误差将超过一个数量级。

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本文引用的文献

1
Multiple-mutation theory of carcinogenesis.癌症发生的多突变理论。
Nature. 1958 Mar 1;181(4609):651-2. doi: 10.1038/181651b0.

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