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Shaojie Wei

Publications and source records attributed to Shaojie Wei.

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Assessing Interactive Causes of an Occurred Outcome Due to Two Binary Exposures

In contrast to evaluating treatment effects, causal attribution analysis focuses on identifying the key factors responsible for an observed outcome. For two binary exposure variables and a binary outcome variable, researchers need to assess not only the likelihood that an observed outcome was caused by a particular exposure, but also the likelihood that it resulted from the interaction between the two exposures. For example, in the case of a male worker who smoked, was exposed to asbestos, and developed lung cancer, researchers aim to explore whether the cancer resulted from smoking, asbestos exposure, or their interaction. Even in randomized controlled trials, widely regarded as the gold standard for causal inference, identifying and evaluating retrospective causal interactions between two exposures remains challenging. In this paper, we define posterior probabilities to characterize the interactive causes of an observed outcome. We establish the identifiability of posterior probabilities by using a secondary outcome variable that may appear after the primary outcome. We apply the proposed method to the classic case of smoking and asbestos exposure. Our results indicate that for lung cancer patients who smoked and were exposed to asbestos, the disease is primarily attributable to the synergistic effect between smoking and asbestos exposure.

stat.AP

Matching-Based Nonparametric Estimation of Group Average Treatment Effects

Heterogeneous treatment effects, which vary according to individual covariates, are crucial in fields such as personalized medicine and tailored treatment strategies. In many applications, rather than considering the heterogeneity induced by all covariates, practitioners focus on a few key covariates to develop tailored treatment decisions. Based on this, we aim to estimate the group average treatment effects (GATEs), which represent heterogeneous treatment effects across subpopulations defined by certain key covariates. Previous strategies for estimating GATEs, such as weighting-based and regression-based methods, suffer from instability or extrapolation bias, especially when several propensity scores are close to zero or one. To address these limitations, we propose two novel nonparametric estimation methods: a matching-based method and a bias-corrected matching method for estimating GATEs. The matching-based method imputes potential outcomes using a matching technique, followed by a nonparametric regression. This method avoids the instability caused by extreme propensity scores but may introduce non-negligible bias when the dimension of full covariates is high. To mitigate this, the bias-corrected matching estimator incorporates additional outcome regression models, enhancing robustness and reducing bias. We show the consistency, double robustness, and asymptotic normality of the bias-corrected matching estimator. We empirically demonstrate the advantages of the proposed methods with extensive simulation studies and a real-world application. An open-source R package, MatchGATE, is available to implement the proposed methods.

stat.ME