Identification and estimation of causal effects with outcomes truncated by death
死亡截断结局下因果效应的识别与估计AI 解读 ↓
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死亡截断结局下因果效应的识别与估计AI 解读 ↓
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It is common in medical studies that the outcome of interest is truncated by death, meaning that a subject has died before the outcome could be measured. In this case, restricted analysis among survivors may be subject to selection bias. Hence, it is of interest to estimate the survivor average causal effect, defined as the average causal effect among the subgroup consisting of subjects who would survive under either exposure. In this paper, we consider the identification and estimation problems of the survivor average causal effect. We propose to use a substitution variable in place of the latent membership in the always-survivor group. The identification conditions required for a substitution variable are conceptually similar to conditions for a conditional instrumental variable, and may apply to both randomized and observational studies. We show that the survivor average causal effect is identifiable with use of such a substitution variable, and propose novel model parameterizations for estimation of the survivor average causal effect under our identification assumptions. Our approaches are illustrated via simulation studies and a data analysis.
Two frequent approaches for identifying structural VARs are external instruments, which carry economic content but are often weak, and non-Gaussianity of the shocks, which provides statistical identification but carries no economic meaning. We combine the two strategies in a single generalized method of moments framework. This hybrid approach point-identifies the target shocks while also identifying the non-target shocks up to sign and ordering. Under suitable rank…
IV-LASSO 的工具变量字典与惩罚选择
Estimating the first stage of an instrumental variables (IV) model with the least absolute shrinkage and selection operator (LASSO) requires choosing a dictionary of technical instruments and a penalty level. First-order asymptotic theory offers no guidance on these choices, as any consistent implementation yields a structural parameter estimator with the same limiting distribution. In finite samples, however, these choices can have a substantial impact on the resulting…
嵌套工具变量分析:转换者平均处理效应及可推广性
Instrumental variables (IVs) are widely used to estimate causal effects from non-randomized data. A canonical example is a randomized trial with noncompliance, in which the randomized treatment assignment serves as an IV for the non-ignorable treatment received. Under a monotonicity assumption, a valid IV nonparametrically identifies the average treatment effect among a latent complier subgroup, whose generalizability is often under debate. In many studies, there exist…
借助知识迁移增强代表性不足子群体的工具变量分析
Instrumental variable (IV) analysis in underrepresented target populations suffers from low statistical efficiency and weak IV bias due to limited sample size. Leveraging external knowledge from a source population with larger samples offers an appealing solution to this problem. We propose in this paper the KNowledge-powered IV Estimator for underrepresented Subpopulations (KNIVES), a framework that enhances the IV analysis for underrepresented subpopulations by…
Instrumental variable (IV) methods mitigate bias from unobserved confounding in observational causal inference but rely on the availability of a valid instrument, which can often be difficult or infeasible to identify in practice. In this paper, we propose a representation learning approach that constructs instrumental representations from observed covariates, which could enable IV-based estimation even in the absence of an explicit instrument. Our model (ZNet) achieves this…
全正编码下的 INSIDE 假设:解释与部分经验评估
Mendelian randomisation (MR) implemented through instrumental variable (IV) analysis is a popular strategy for strengthening causal inference in observational studies. A key assumption for several MR estimators, including MR-Egger regression, is the INstrument Strength Independent of Direct Effect (INSIDE) assumption. However, there is no established empirical test for assessing the plausibility of this assumption. Moreover, INSIDE depends on how genetic variants are coded…