基于目标最大似然的因果推理:第一部分

IF 1.2 4区 数学
M. J. van der Laan
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引用次数: 93

摘要

给定因果图假设,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的可能性进行这些干预而获得的。获得的g计算公式表示,如果对生成数据的系统强制执行这种干预,数据将具有的反事实分布。兴趣的因果效应现在可以定义为这些由不同干预措施索引的反事实分布之间的一些差异。例如,干预措施可以代表静态治疗方案或个性化治疗规则,根据时间相关协变量分配治疗,因果效应可以根据治疗方案特定反事实结果的平均值作为相应治疗方案的函数的特征来定义。这些特征可以根据所谓的静态或个性化治疗规则的(非参数)边际结构模型来非参数地定义,其参数可以被认为是治疗方案特定反事实分布之间差异的(平滑)总结度量。在本文中,我们开发了一个特定的目标最大似然估计多时间点干预的因果效应。这涉及到使用基于损失的超级学习来获得g计算公式中未知因素的初始估计,随后,对每个估计的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),用最大似然估计估计波动参数,并迭代初始因素的更新步骤直到收敛。这种迭代的目标最大似然更新步骤使得因果效应的结果估计量具有双重鲁棒性,即如果初始估计量一致,或者最优波动函数的估计量一致,则结果估计量是一致的。如果正确指定了因果图中节点的条件分布,则正确指定了最优波动函数。后一种条件分布通常包括所谓的处理和审查机制。在不同的目标最大似然估计器(例如,由不同的初始估计器索引)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。文中提到了一些具体的损失函数。随后,对这种有针对性的最大似然估计过程进行了各种有趣的观察。本文为后续的第二部分文章提供了基础,其中提供了在复杂因果效应估计问题中实现目标MLE的具体演示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeted Maximum Likelihood Based Causal Inference: Part I
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.
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来源期刊
International Journal of Biostatistics
International Journal of Biostatistics Mathematics-Statistics and Probability
CiteScore
2.30
自引率
8.30%
发文量
28
期刊介绍: The International Journal of Biostatistics (IJB) seeks to publish new biostatistical models and methods, new statistical theory, as well as original applications of statistical methods, for important practical problems arising from the biological, medical, public health, and agricultural sciences with an emphasis on semiparametric methods. Given many alternatives to publish exist within biostatistics, IJB offers a place to publish for research in biostatistics focusing on modern methods, often based on machine-learning and other data-adaptive methodologies, as well as providing a unique reading experience that compels the author to be explicit about the statistical inference problem addressed by the paper. IJB is intended that the journal cover the entire range of biostatistics, from theoretical advances to relevant and sensible translations of a practical problem into a statistical framework. Electronic publication also allows for data and software code to be appended, and opens the door for reproducible research allowing readers to easily replicate analyses described in a paper. Both original research and review articles will be warmly received, as will articles applying sound statistical methods to practical problems.
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