van der Laan Mark J
University of California - Berkeley, CA, USA.
Int J Biostat. 2010;6(2):Article 2. doi: 10.2202/1557-4679.1211.
Given causal graph assumptions, intervention-specific counterfactual distributions of the data can be defined by the so called G-computation formula, which is obtained by carrying out these interventions on the likelihood of the data factorized according to the causal graph. The obtained G-computation formula represents the counterfactual distribution the data would have had if this intervention would have been enforced on the system generating the data. A causal effect of interest can now be defined as some difference between these counterfactual distributions indexed by different interventions. For example, the interventions can represent static treatment regimens or individualized treatment rules that assign treatment in response to time-dependent covariates, and the causal effects could be defined in terms of features of the mean of the treatment-regimen specific counterfactual outcome of interest as a function of the corresponding treatment regimens. Such features could be defined nonparametrically in terms of so called (nonparametric) marginal structural models for static or individualized treatment rules, whose parameters can be thought of as (smooth) summary measures of differences between the treatment regimen specific counterfactual distributions. In this article, we develop a particular targeted maximum likelihood estimator of causal effects of multiple time point interventions. This involves the use of loss-based super-learning to obtain an initial estimate of the unknown factors of the G-computation formula, and subsequently, applying a target-parameter specific optimal fluctuation function (least favorable parametric submodel) to each estimated factor, estimating the fluctuation parameter(s) with maximum likelihood estimation, and iterating this updating step of the initial factor till convergence. This iterative targeted maximum likelihood updating step makes the resulting estimator of the causal effect double robust in the sense that it is consistent if either the initial estimator is consistent, or the estimator of the optimal fluctuation function is consistent. The optimal fluctuation function is correctly specified if the conditional distributions of the nodes in the causal graph one intervenes upon are correctly specified. The latter conditional distributions often comprise the so called treatment and censoring mechanism. Selection among different targeted maximum likelihood estimators (e.g., indexed by different initial estimators) can be based on loss-based cross-validation such as likelihood based cross-validation or cross-validation based on another appropriate loss function for the distribution of the data. Some specific loss functions are mentioned in this article. Subsequently, a variety of interesting observations about this targeted maximum likelihood estimation procedure are made. This article provides the basis for the subsequent companion Part II-article in which concrete demonstrations for the implementation of the targeted MLE in complex causal effect estimation problems are provided.
在给定因果图假设的情况下,数据的特定干预反事实分布可以通过所谓的G计算公式来定义,该公式是通过对根据因果图分解的数据似然性进行这些干预而获得的。所得到的G计算公式表示如果对生成数据的系统实施此干预,数据本应具有的反事实分布。现在,可以将感兴趣的因果效应定义为这些由不同干预索引的反事实分布之间的某种差异。例如,干预可以表示静态治疗方案或根据随时间变化的协变量分配治疗的个体化治疗规则,并且因果效应可以根据感兴趣的治疗方案特定反事实结果的均值特征作为相应治疗方案的函数来定义。此类特征可以根据用于静态或个体化治疗规则的所谓(非参数)边际结构模型进行非参数定义,其参数可以被视为治疗方案特定反事实分布之间差异的(平滑)汇总度量。在本文中,我们开发了一种针对多个时间点干预因果效应的特定靶向最大似然估计器。这涉及使用基于损失的超学习来获得G计算公式未知因素的初始估计,随后,对每个估计因素应用目标参数特定的最优波动函数(最不利参数子模型),使用最大似然估计来估计波动参数,并迭代此初始因素的更新步骤直至收敛。这种迭代的靶向最大似然更新步骤使得所得的因果效应估计器具有双重稳健性,即如果初始估计器是一致的,或者最优波动函数的估计器是一致的,那么它就是一致的。如果对其进行干预的因果图中节点的条件分布被正确指定,则最优波动函数被正确指定。后者的条件分布通常包括所谓的治疗和删失机制。不同靶向最大似然估计器(例如,由不同初始估计器索引)之间的选择可以基于基于损失的交叉验证,例如基于似然的交叉验证或基于数据分布的另一个适当损失函数的交叉验证。本文提到了一些特定的损失函数。随后,对这种靶向最大似然估计程序进行了各种有趣的观察。本文为后续的配套第二部分文章提供了基础,在该文章中提供了在复杂因果效应估计问题中实施靶向最大似然估计的具体示例。