Yang Shu, Lok Judith J
Department of Statistics, North Carolina State University, Raleigh, NC 27695, USA.
Department of Biostatistics, Harvard University, Massachusetts, MA 02115, USA.
Stat Sin. 2018 Oct;28(4):1703-1723. doi: 10.5705/ss.202016.0133.
Coarse Structural Nested Mean Models (SNMMs, Robins (2000)) and G-estimation can be used to estimate the causal effect of a time-varying treatment from longitudinal observational studies. However, they rely on an untestable assumption of no unmeasured confounding. In the presence of unmeasured confounders, the unobserved potential outcomes are not missing at random, and standard G-estimation leads to biased effect estimates. To remedy this, we investigate the sensitivity of G-estimators of coarse SNMMs to unmeasured confounding, assuming a nonidentifiable bias function which quantifies the impact of unmeasured confounding on the average potential outcome. We present adjusted G-estimators of coarse SNMM parameters and prove their consistency, under the bias modeling for unmeasured confounding. We apply this to a sensitivity analysis for the effect of the ART initiation time on the mean CD4 count at year 2 after infection in HIV-positive patients, based on the prospective Acute and Early Disease Research Program.
粗结构嵌套均值模型(SNMMs,罗宾斯(2000年))和G估计可用于从纵向观察性研究中估计时变治疗的因果效应。然而,它们依赖于不可检验的无未测量混杂因素的假设。在存在未测量混杂因素的情况下,未观察到的潜在结果并非随机缺失,标准的G估计会导致有偏差的效应估计。为了纠正这一点,我们研究了粗SNMMs的G估计量对未测量混杂因素的敏感性,假设一个不可识别的偏差函数,该函数量化了未测量混杂因素对平均潜在结果的影响。我们提出了粗SNMM参数的调整后G估计量,并在未测量混杂因素的偏差建模下证明了它们的一致性。我们将此应用于一项敏感性分析,该分析基于前瞻性急性和早期疾病研究项目,研究抗逆转录病毒治疗(ART)开始时间对HIV阳性患者感染后第2年平均CD4细胞计数的影响。