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Correcting for Measurement Error in Time-Varying Covariates in Marginal Structural Models

机译:边际结构模型中时变协变量的测量误差校正

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摘要

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.
机译:从边际结构模型(MSM)对因果参数进行无偏估计需要一个基本假设,即没有不可测量的混淆。不幸的是,用于获得逆概率权重的时变协变量通常容易出错。尽管已知重要混杂因素中的大量测量误差会破坏常规未加权回归模型中混杂因素的控制,但是在MSM文献中,此问题受到的关注相对有限。在这里,我们提出了一种模拟外推(SIMEX)过程的新颖应用,以解决时变协变量中的测量误差,并比较了两种方法。基于SIMEX的校正的直接方法以结果模型参数为目标,而间接方法则校正使用暴露模型估算的权重。我们在不同的临床合理假设下评估拟议方法在模拟中的性能。仿真表明,随时间变化的协变量中的测量误差可能会在MSM估计器中引起时变暴露的因果效应,从而产生实质性偏差,并且两种建议的SIMEX方法在具有低度至中度误差的情况下,都能产生几乎无偏差的估计。我们使用加拿大共感染队列研究收集的数据,通过对丙型肝炎病毒感染者之间持续的病毒学应答和肝纤维化进程之间的关系进行简单分析,说明了该方法,同时考虑了γ-谷氨酰转移酶的测量误差。 2003年至2014年。

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