Department of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, 1518 Clifton Rd., Atlanta, GA, USA.
Center for Financing, Access, and Cost Trends, Agency for Healthcare Research and Quality, 5600 Fishers Lane, Rockville, MD, USA.
Biostatistics. 2021 Apr 10;22(2):250-265. doi: 10.1093/biostatistics/kxz028.
Measuring a biomarker in pooled samples from multiple cases or controls can lead to cost-effective estimation of a covariate-adjusted odds ratio, particularly for expensive assays. But pooled measurements may be affected by assay-related measurement error (ME) and/or pooling-related processing error (PE), which can induce bias if ignored. Building on recently developed methods for a normal biomarker subject to additive errors, we present two related estimators for a right-skewed biomarker subject to multiplicative errors: one based on logistic regression and the other based on a Gamma discriminant function model. Applied to a reproductive health dataset with a right-skewed cytokine measured in pools of size 1 and 2, both methods suggest no association with spontaneous abortion. The fitted models indicate little ME but fairly severe PE, the latter of which is much too large to ignore. Simulations mimicking these data with a non-unity odds ratio confirm validity of the estimators and illustrate how PE can detract from pooling-related gains in statistical efficiency. These methods address a key issue associated with the homogeneous pools study design and should facilitate valid odds ratio estimation at a lower cost in a wide range of scenarios.
在多个病例或对照的混合样本中测量生物标志物可以有效地估计协变量调整后的优势比,特别是对于昂贵的检测方法。但是,混合测量可能会受到与检测相关的测量误差 (ME) 和/或与混合相关的处理误差 (PE) 的影响,如果忽略这些误差,可能会导致偏差。基于最近开发的针对加性误差的正常生物标志物的方法,我们为受乘性误差影响的右偏生物标志物提出了两种相关的估计器:一种基于逻辑回归,另一种基于伽玛判别函数模型。将这两种方法应用于一个具有右偏细胞因子的生殖健康数据集,该数据集的细胞因子在大小为 1 和 2 的混合体中进行测量,两种方法均表明与自然流产无关。拟合模型表明 ME 很小,但 PE 相当严重,后者大到不容忽视。模拟这些数据的非单位比值的模拟表明估计器是有效的,并说明了 PE 如何削弱与混合相关的统计效率的提高。这些方法解决了与同质池研究设计相关的一个关键问题,并且应该能够在广泛的情况下以更低的成本有效地估计优势比。