A probabilistic framework for non-cancer risk assessment

被引:10
|
作者
Chen, James J. [1 ]
Moon, Hojin [1 ]
Kodell, Ralph L. [1 ]
机构
[1] US FDA, Natl Ctr Toxicol Res, Div Biometry & Risk Assessment, Jefferson, AR 72079 USA
关键词
benchmark dose; distribution of exposure; hierarchical model; interspecies and intraspecies uncertainties; point of departure;
D O I
10.1016/j.yrtph.2006.10.008
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
Risk assessment involves an analysis of the relationship between exposure and health related outcomes to derive an allowable exposure level or to estimate a low-dose risk. Acceptable levels of human exposure for non-cancer effects generally are derived by dividing an experimental no-observed-adverse-effect-level or a lower confidence limit benchmark dose by a product of several uncertainty factors. This paper presents a hierarchical modeling framework for a probabilistic approach to non-cancer risk assessment. The hierarchical model integrates the distributions of uncertainty factors and the distribution of the actual exposure level to construct the dose-response model for the proportion of population at risk and the dose-response model for the expected proportion of population at risk for a given exposure distribution. The proposed approach is based on the use of the BMDL (lower confidence limit on the benchmark dose) as a POD (point of departure) for risk assessment of non-cancer effects. Published by Elsevier Inc.
引用
收藏
页码:45 / 50
页数:6
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