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Extending the case–control design to longitudinal data: stratified sampling based on repeated binary outcomes

机译:将病例控制设计扩展到纵向数据:基于重复二元结果的分层抽样

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摘要

We detail study design options that generalize case–control sampling when longitudinal outcome data are already collected as part of a primary cohort study, but new exposure data must be retrospectively processed for a secondary analysis. Furthermore, we assume that cost will limit the size of the subsample that can be evaluated. We describe a novel class of stratified outcome–dependent sampling designs for longitudinal binary response data where distinct strata are created for subjects who never, sometimes, and always experienced the event of interest during longitudinal follow-up. Individual designs within this class are differentiated by the stratum-specific sampling probabilities. We show for parameters associated with time-varying exposures, subjects who experience the event/outcome at some but not at all of the follow-up times (i.e., those who exhibit response variation) are highly informative. If the time-varying exposure varies exclusively within individuals (i.e., intraclass correlation coefficient is 0), then sampling all subjects with response variability can yield highly precise parameter estimates even when compared to an analysis of the original cohort. The flexibility of the designs and analysis procedures also permits estimation of parameters that correspond to time-fixed covariates, and we show that with an imputation–based estimation procedure, baseline covariate associations can be estimated with very high precision irrespective of the design. We demonstrate features of the designs and analysis procedures via a plasmode simulation using data from the Lung Health Study.
机译:我们详细介绍了研究设计方案,这些研究方案可以在主要队列研究已经收集了纵向结果数据时对病例对照抽样进行一般化,但是必须追溯处理新的暴露数据以进行次要分析。此外,我们假设成本将限制可以评估的子样本的大小。我们描述了针对纵向二进制响应数据的一类新颖的,基于分层结果的抽样设计,其中为在纵向随访期间从未,有时且始终经历感兴趣事件的受试者创建了不同的层次。此类中的各个设计通过特定于层的采样概率来区分。对于与时变暴露量相关的参数,我们显示了在某些但并非所有随访时间都经历事件/结果的受试者(即那些表现出反应差异的受试者)具有丰富的信息。如果随时间变化的暴露仅在个体内变化(即类内相关系数为0),则即使与原始队列的分析相比,对具有响应变异性的所有对象进行采样也可以得出高度精确的参数估计值。设计和分析程序的灵活性还允许估计与固定时间的协变量相对应的参数,并且我们表明,使用基于归因的估计程序,无论设计如何,都可以非常高精度地估计基线协变量关联。我们通过使用来自肺部健康研究的数据的等离子体模拟展示了设计和分析程序的功能。

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