Systematic dose-response of environmental epidemiologic studies: Dose and response pre-analysis

被引:10
|
作者
Allen, Bruce
Shao, Kan [1 ]
Hobbie, Kevin [2 ]
Mendez, William, Jr. [2 ]
Lee, Janice S. [3 ]
Cote, Ila [3 ]
Druwe, Ingrid [3 ]
Gift, Jeff [3 ]
Davis, J. Allen [4 ]
机构
[1] Indiana Univ, Dept Environm Hlth, Bloomington, IN USA
[2] ICF, 9300 Lee Highway, Fairfax, VA 22031 USA
[3] US EPA, Ctr Publ Hlth & Environm Assessment, Res Triangle Pk, NC USA
[4] US EPA, Ctr Publ Hlth & Environm Assessment, Washington, DC 20460 USA
关键词
Dose conversion; Inter-individual variability; Uncertainty; Dose-response; Meta-analysis; DRINKING-WATER; RISK; CANCER; RESIDENTS; EXPOSURE; LEVEL;
D O I
10.1016/j.envint.2020.105810
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Meta-analysis approaches can be used to assess the human risks due to exposure to environmental chemicals when there are numerous high-quality epidemiologic studies of priority outcomes in a database. However, methodological issues related to how different studies report effect measures and incorporate exposure into their analyses arise that complicate the pooled analysis of multiple studies. As such, there are "pre-analysis" steps that are often necessary to prepare summary data reported in epidemiologic studies for dose-response analysis. This paper uses epidemiologic studies of arsenic-induced health effects as a case example and addresses the issues surrounding the estimation of mean doses from censored dose- or exposure-intervals reported in the literature (e.g., estimation of mean doses from high exposures that are only reported as an open-ended interval), calculation of a common dose metric for use in a dose-response meta-analysis (one that takes into consideration inter-individual variability), and calculation of response "effective counts" that inherently account for confounders. The methods herein may be generalizable to 1) the analysis of other environmental contaminants with a suitable database of epidemiologic studies, and 2) any meta-analytic approach used to pool information across studies. A second companion paper detailing the use of "pre-analyzed" data in a hierarchical Bayesian dose-response model and techniques for extrapolating risks to target populations follows.
引用
收藏
页数:11
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