Toward Making Epidemiologic Data More Useful for Quantitative Risk Assessment

K. Crump, B. Allen
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引用次数: 5

Abstract

This paper discusses issues faced in using epidemiologic data to develop quantitative estimates of risk from specified patterns of exposure to a toxicant. We focus on use of data from cohort studies with binary endpoints (occurrence or non-occurrence of disease). Relative advantages of Cox regression and Poisson regression are presented. A general form of exposure metric is presented, and criteria for selecting an appropriate metric are discussed. Advantages and disadvantages of various dose-response models are discussed. It is argued that, unless low-dose linearity of the dose response can be ruled out on non-statistical grounds, then bounds for low-dose risk should incorporate low-dose linearity; a sequential procedure for computing such bounds is illustrated. Limitations in exposure data and their impact on risk assessments are discussed. Issues arising when using meta-analytic techniques to combine data from multiple epidemiologic studies are discussed. Limitations in risk assessments resulting from reliance upon published results alone are described. Methods for converting from measures of risk used in epidemiologic studies (e.g., relative risk) to measures appropriate for a risk assessment (e.g., additional lifetime probability of disease occurrence resulting from a specific exposure pattern) are described in detail. Several examples from the asbestos epidemiologic literature are presented to illustrate these issues.
使流行病学数据对定量风险评估更有用
本文讨论了在使用流行病学数据对暴露于某种毒物的特定模式的风险进行定量估计时所面临的问题。我们着重于使用具有双终点(发生或不发生疾病)的队列研究的数据。介绍了Cox回归和泊松回归的相对优势。提出了暴露度量的一般形式,并讨论了选择适当度量的标准。讨论了各种剂量反应模型的优缺点。有人认为,除非剂量反应的低剂量线性可以根据非统计理由排除,否则低剂量风险界限应包括低剂量线性;文中举例说明了计算这种边界的顺序过程。讨论了暴露数据的局限性及其对风险评估的影响。讨论了当使用元分析技术结合多个流行病学研究的数据时出现的问题。描述了仅依赖已发表的结果而造成的风险评估的局限性。详细描述了从流行病学研究中使用的风险度量(例如,相对风险)转换为适合于风险评估的度量(例如,由特定暴露模式导致的疾病发生的额外终生概率)的方法。本文从石棉流行病学文献中举出几个例子来说明这些问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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