Tang Li, Lyles Robert H, Ye Ye, Lo Yungtai, King Caroline C
Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Department of Biostatistics and Bioinformatics, Rollins School of Public Health of Emory University, Atlanta, GA 30322, USA.
Epidemiol Methods. 2013 Sep 1;2(1):49-66. doi: 10.1515/em-2013-0008.
The problem of misclassification is common in epidemiological and clinical research. In some cases, misclassification may be incurred when measuring both exposure and outcome variables. It is well known that validity of analytic results (e.g. point and confidence interval estimates for odds ratios of interest) can be forfeited when no correction effort is made. Therefore, valid and accessible methods with which to deal with these issues remain in high demand. Here, we elucidate extensions of well-studied methods in order to facilitate misclassification adjustment when a binary outcome and binary exposure variable are both subject to misclassification. By formulating generalizations of assumptions underlying well-studied "matrix" and "inverse matrix" methods into the framework of maximum likelihood, our approach allows the flexible modeling of a richer set of misclassification mechanisms when adequate internal validation data are available. The value of our extensions and a strong case for the internal validation design are demonstrated by means of simulations and analysis of bacterial vaginosis and trichomoniasis data from the HIV Epidemiology Research Study.
错误分类问题在流行病学和临床研究中很常见。在某些情况下,测量暴露变量和结局变量时都可能出现错误分类。众所周知,如果不进行校正,分析结果的有效性(例如,感兴趣的比值比的点估计和置信区间估计)可能会丧失。因此,仍然迫切需要有效且易于使用的方法来处理这些问题。在此,我们阐明了经过充分研究的方法的扩展,以便在二元结局和二元暴露变量都存在错误分类时便于进行错误分类调整。通过将经过充分研究的“矩阵”和“逆矩阵”方法所依据的假设推广到最大似然框架中,当有足够的内部验证数据时,我们的方法允许对更丰富的错误分类机制进行灵活建模。通过对来自HIV流行病学研究的细菌性阴道病和滴虫病数据进行模拟和分析,证明了我们扩展方法的价值以及内部验证设计的有力理由。