Department of Biostatistics, School of Public Health, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan.
Division of Medical Statistics, Department of Social Medicine, Faculty of Medicine, Toho University, Ota-ku, Tokyo 143-8540, Japan.
Biometrics. 2024 Jan 29;80(1). doi: 10.1093/biomtc/ujae005.
When estimating the causal effects of time-varying treatments on survival in nested case-control (NCC) studies, marginal structural Cox models (Cox-MSMs) with inverse probability weights (IPWs) are a natural approach. However, calculating IPWs from the cases and controls is difficult because they are not random samples from the full cohort, and the number of subjects may be insufficient for calculation. To overcome these difficulties, we propose a method for calculating IPWs to fit Cox-MSMs to NCC sampling data. We estimate the IPWs using a pseudo-likelihood estimation method with an inverse probability of sampling weight using NCC samples, and additional samples of subjects who experience treatment changes and subjects whose follow-up is censored are required to calculate the weights. Our method only requires covariate histories for the samples. The confidence intervals are calculated from the robust variance estimator for the NCC sampling data. We also derive the asymptotic properties of the estimator of Cox-MSM under NCC sampling. The proposed methods will allow researchers to apply several case-control matching methods to improve statistical efficiency. A simulation study was conducted to evaluate the finite sample performance of the proposed method. We also applied our method to a motivating pharmacoepidemiological study examining the effect of statins on the incidence of coronary heart disease. The proposed method may be useful for estimating the causal effects of time-varying treatments in NCC studies.
在嵌套病例对照(NCC)研究中估计时变治疗对生存的因果效应时,逆概率加权(IPW)的边际结构 Cox 模型(Cox-MSM)是一种自然的方法。然而,从病例和对照中计算 IPW 是困难的,因为它们不是来自整个队列的随机样本,并且可能没有足够的受试者数量进行计算。为了克服这些困难,我们提出了一种计算 IPW 的方法,以适应 Cox-MSM 到 NCC 抽样数据。我们使用逆概率抽样权重的拟似然估计方法估计 IPW,并使用 NCC 样本和经历治疗变化的受试者和随访被删失的受试者的额外样本来计算权重。我们的方法仅需要样本的协变量历史记录。置信区间是从 NCC 抽样数据的稳健方差估计量计算得出的。我们还推导出了在 NCC 抽样下 Cox-MSM 估计量的渐近性质。所提出的方法将允许研究人员应用几种病例对照匹配方法来提高统计效率。进行了一项模拟研究,以评估所提出方法的有限样本性能。我们还将我们的方法应用于一项动机性药物流行病学研究,以检验他汀类药物对冠心病发病率的影响。该方法可能有助于在 NCC 研究中估计时变治疗的因果效应。