🤖 AI Summary
This study addresses key challenges in synthesizing causal evidence from heterogeneous sources—namely, individual-level and aggregate-level data—including poor integrability of treatment effects across target populations, limited transportability, and insufficient personalization. To this end, we propose a target-population-characteristic-aware weighted evidence synthesis framework. Our method innovatively introduces a sample-bounded weighting scheme to enable customized meta-analysis; develops a principled approach to identify studies whose populations deviate from the target, thereby enhancing robustness and interpretability; and integrates causal inference with meta-analytic principles, ensuring asymptotic normality of the estimator under multiple consistency conditions. Simulation studies and real-data analyses demonstrate that the proposed weighted estimation method significantly improves both accuracy and personalization of treatment effect estimation, outperforming conventional regression-based meta-analytic approaches.
📝 Abstract
Over the past few decades, statistical methods for causal inference have made impressive strides, enabling progress across a range of scientific fields. However, these methodological advances have often been confined to individual studies, limiting their ability to draw more generalizable conclusions. Achieving a thorough understanding of cause and effect typically relies on the integration, reconciliation, and synthesis from diverse study designs and multiple data sources. Furthermore, it is crucial to direct this synthesis effort toward understanding the effect of treatments for specific patient populations. To address these challenges, we present a weighting framework for evidence synthesis that handles both individual- and aggregate-level data, encompassing and extending conventional regression-based meta-analysis methods. We use this approach to tailor meta-analyses, targeting the covariate profiles of patients in a target population in a sample-bounded manner, thereby enhancing their personalization and robustness. We propose a technique to detect studies that meaningfully deviate from the target population, suggesting when it might be prudent to exclude them from the analysis. We establish multiple consistency conditions and demonstrate asymptotic normality for the proposed estimator. We illustrate this approach using simulated and real data.