SearcharxivSearch

arXiv subjects

Jay Jojo Cheng

Publications and source records attributed to Jay Jojo Cheng.

2 recordsLinked to original sources

Causal Generalization of Continuous Treatment Effects under Covariate Shift

Average dose-response functions are widely used to summarize causal effects of continuous treatments, but most existing methods assume that the observed sample represents the target population. We study a covariate-shift setting in which covariates, treatment, and outcome are observed in a labelled source sample, while only covariates are observed in the target sample. We develop a two-sample local polynomial regression framework based on pseudo-outcomes that use source outcomes to address confounding and target covariates to define the population of interest. We further propose a source-to-target extension of distance covariance optimal weighting (DCOW), designed to remove treatment-covariate dependence in the source sample while aligning the weighted source covariate distribution with the target population. A central theoretical contribution is a weight-level analysis of this optimization-based procedure: we show that the population criterion identifies the oracle source-to-target weights and that approximate empirical minimizers, including exact minimizers as a special case, converge uniformly to these weights under regularity conditions. We also establish consistency and asymptotic normality of the resulting estimator. Simulations show that the proposed method improves target dose-response estimation relative to DCOW, generalized-propensity-score weighting, entropy balancing, and unweighted alternatives. We illustrate the method in a county-level analysis of PM2.5 exposure and subsequent heart-disease mortality using a source-target validation design.

stat.ME

Meta-analysis of individualized treatment rules via sign-coherency

Medical treatments tailored to a patient's baseline characteristics hold the potential of improving patient outcomes while reducing negative side effects. Learning individualized treatment rules (ITRs) often requires aggregation of multiple datasets(sites); however, current ITR methodology does not take between-site heterogeneity into account, which can hurt model generalizability when deploying back to each site. To address this problem, we develop a method for individual-level meta-analysis of ITRs, which jointly learns site-specific ITRs while borrowing information about feature sign-coherency via a scientifically-motivated directionality principle. We also develop an adaptive procedure for model tuning, using information criteria tailored to the ITR learning problem. We study the proposed methods through numerical experiments to understand their performance under different levels of between-site heterogeneity and apply the methodology to estimate ITRs in a large multi-center database of electronic health records. This work extends several popular methodologies for estimating ITRs (A-learning, weighted learning) to the multiple-sites setting.

stat.ML