Measurement error in biomarkers: sources, assessment, and impact on studies.

IARC scientific publications Pub Date : 2011-01-01
Emily White
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Abstract

Measurement error in a biomarker refers to the error of a biomarker measure applied in a specific way to a specific population, versus the true (etiologic) exposure. In epidemiologic studies, this error includes not only laboratory error, but also errors (variations) introduced during specimen collection and storage, and due to day-to-day, month-to-month, and year-to-year within-subject variability of the biomarker. Validity and reliability studies that aim to assess the degree of biomarker error for use of a specific biomarker in epidemiologic studies must be properly designed to measure all of these sources of error. Validity studies compare the biomarker to be used in an epidemiologic study to a perfect measure in a group of subjects. The parameters used to quantify the error in a binary marker are sensitivity and specificity. For continuous biomarkers, the parameters used are bias (the mean difference between the biomarker and the true exposure) and the validity coefficient (correlation of the biomarker with the true exposure). Often a perfect measure of the exposure is not available, so reliability (repeatability) studies are conducted. These are analysed using kappa for binary biomarkers and the intraclass correlation coefficient for continuous biomarkers. Equations are given which use these parameters from validity or reliability studies to estimate the impact of nondifferential biomarker measurement error on the risk ratio in an epidemiologic study that will use the biomarker. Under nondifferential error, the attenuation of the risk ratio is towards the null and is often quite substantial, even for reasonably accurate biomarker measures. Differential biomarker error between cases and controls can bias the risk ratio in any direction and completely invalidate an epidemiologic study.

生物标记物的测量误差:来源、评估和对研究的影响。
生物标志物的测量误差是指以特定方式应用于特定人群的生物标志物测量与真实(病因学)暴露的误差。在流行病学研究中,这种误差不仅包括实验室误差,还包括在标本采集和储存过程中引入的误差(变异),以及由于生物标志物的日常、逐月和逐年的受试者变异性而引起的误差(变异)。效度和信度研究旨在评估在流行病学研究中使用特定生物标志物的生物标志物误差程度,必须适当设计以测量所有这些误差来源。效度研究将流行病学研究中使用的生物标志物与一组受试者的完美测量进行比较。用于量化二元标记误差的参数是灵敏度和特异性。对于连续生物标记物,使用的参数是偏差(生物标记物与真实暴露之间的平均差值)和效度系数(生物标记物与真实暴露的相关性)。通常没有完美的暴露测量方法,因此需要进行可靠性(可重复性)研究。用kappa分析二元生物标记物,用类内相关系数分析连续生物标记物。给出了使用这些效度或信度研究参数的方程,以估计将使用生物标志物的流行病学研究中非差异生物标志物测量误差对风险比的影响。在非微分误差下,即使对于相当准确的生物标志物测量,风险比的衰减也趋于零,并且通常相当可观。病例和对照组之间的差异生物标志物误差可以使风险比向任何方向偏倚,并使流行病学研究完全无效。
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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