Kyle Ryan P, Moodie Erica E M, Klein Marina B, Abrahamowicz Michał
Am J Epidemiol. 2016 Aug 1;184(3):249-58. doi: 10.1093/aje/kww068. Epub 2016 Jul 13.
Unbiased estimation of causal parameters from marginal structural models (MSMs) requires a fundamental assumption of no unmeasured confounding. Unfortunately, the time-varying covariates used to obtain inverse probability weights are often error-prone. Although substantial measurement error in important confounders is known to undermine control of confounders in conventional unweighted regression models, this issue has received comparatively limited attention in the MSM literature. Here we propose a novel application of the simulation-extrapolation (SIMEX) procedure to address measurement error in time-varying covariates, and we compare 2 approaches. The direct approach to SIMEX-based correction targets outcome model parameters, while the indirect approach corrects the weights estimated using the exposure model. We assess the performance of the proposed methods in simulations under different clinically plausible assumptions. The simulations demonstrate that measurement errors in time-dependent covariates may induce substantial bias in MSM estimators of causal effects of time-varying exposures, and that both proposed SIMEX approaches yield practically unbiased estimates in scenarios featuring low-to-moderate degrees of error. We illustrate the proposed approach in a simple analysis of the relationship between sustained virological response and liver fibrosis progression among persons infected with hepatitis C virus, while accounting for measurement error in γ-glutamyltransferase, using data collected in the Canadian Co-infection Cohort Study from 2003 to 2014.
从边际结构模型(MSM)中无偏估计因果参数需要一个无未测量混杂因素的基本假设。不幸的是,用于获得逆概率权重的时变协变量往往容易出错。虽然已知重要混杂因素中的大量测量误差会破坏传统未加权回归模型中混杂因素的控制,但这个问题在MSM文献中受到的关注相对有限。在这里,我们提出了模拟外推法(SIMEX)的一种新应用,以解决时变协变量中的测量误差问题,并且我们比较了两种方法。基于SIMEX的直接校正方法针对结局模型参数,而间接方法校正使用暴露模型估计的权重。我们在不同临床合理假设下的模拟中评估所提出方法的性能。模拟表明,时依协变量中的测量误差可能会在MSM估计时变暴露的因果效应中引起实质性偏差,并且在低至中等误差程度的情况下,两种提出的SIMEX方法都能产生实际无偏的估计。我们使用2003年至2014年加拿大合并感染队列研究中收集的数据,在对丙型肝炎病毒感染者的持续病毒学应答与肝纤维化进展之间的关系进行简单分析时,说明了所提出的方法,同时考虑了γ-谷氨酰转移酶中的测量误差。