Loomis D P, Savitz D A
Department of Epidemiology, School of Public Health, University of North Carolina, Chapel Hill 27599-7400.
Scand J Work Environ Health. 1994 Jun;20(3):200-5. doi: 10.5271/sjweh.1408.
When potentially hazardous agents have multiple environmental sources, failure to include all exposure sources can constitute a type of measurement error. In addition, the effects of exposure from one source can also be confounded by exposure to other sources of the same agent. In this study clarification of these concepts is sought, and the direction and magnitude of the resulting bias in epidemiologic measures of association are examined.
The bias in dose-response functions when the exposure data omit some sources of the agent was estimated with linear and log-linear models to compute risk differences and risk ratios under different assumptions about the magnitude and correlation of exposures from measured and unmeasured sources.
With unmeasured exposure of constant magnitude, there is no bias when a measure of association of the appropriate form (difference measures for additive dose-response processes, ratios for multiplicative ones) is selected. When the magnitude of unmeasured exposure varies, the results is nondifferential measurement error that can bias observed dose-response relations upward or downward, depending on the pattern of measurement error and the measure of association.
Failure to measure all sources of exposure to an agent and account for them in the analysis can bias the results of epidemiologic studies. When it is not feasible to measure all exposure sources, the magnitude of bias can be predicted by estimating the distribution of omitted exposures from external data or substudies. Sensitivity analyses are particularly useful for estimating the direction and magnitude of potential bias from incomplete exposure assessment.
当潜在危险因子存在多种环境来源时,未能纳入所有暴露源可构成一种测量误差。此外,来自一个来源的暴露效应也可能被同一因子的其他来源暴露所混淆。本研究旨在澄清这些概念,并检验流行病学关联测量中由此产生的偏差的方向和大小。
当暴露数据遗漏了因子的某些来源时,使用线性和对数线性模型估计剂量反应函数中的偏差,以计算在关于测量和未测量来源暴露的大小和相关性的不同假设下的风险差异和风险比。
对于恒定大小的未测量暴露,当选择适当形式的关联测量(相加剂量反应过程的差异测量,相乘过程的比值测量)时,不存在偏差。当未测量暴露的大小变化时,结果是无差异测量误差,其可使观察到的剂量反应关系向上或向下偏倚,这取决于测量误差模式和关联测量。
未能测量因子的所有暴露源并在分析中加以考虑,可能会使流行病学研究结果产生偏倚。当测量所有暴露源不可行时,可通过从外部数据或子研究估计遗漏暴露的分布来预测偏倚大小。敏感性分析对于估计不完全暴露评估导致的潜在偏倚的方向和大小特别有用。