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R. Colin Carter

Publications and source records attributed to R. Colin Carter.

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Prenatal alcohol exposure and child cognition: semi-continuous exposures, causal inference and evidence synthesis

We address the challenge of causal inference status and the dose-response effects with a semi-continuous exposure. A two-stage approach is proposed using estimating equation for multiple outcomes with large sample properties derived for the resulting estimators. Homogeneity tests are developed to assess whether causal effects of exposure status and the dose-response effects are the same across multiple outcomes. A global homogeneity test is also developed to assess whether the effect of exposure status (exposed/not exposed) and the dose-response effect of the continuous exposure level are each equal across all outcomes. The methods of estimation and testing are rigorously evaluated in simulation studies and applied to a motivating study on the effects of prenatal alcohol exposure on childhood cognition defined by executive function (EF), academic achievement in math, and learning and memory (LM).

stat.ME

Two-stage Estimation for Causal Inference Involving a Semi-continuous Exposure

Methods for causal inference are well developed for binary and continuous exposures, but in many settings, the exposure has a substantial mass at zero-such exposures are called semi-continuous. We propose a general causal framework for such semi-continuous exposures, together with a novel two-stage estimation strategy. A two-part propensity structure is introduced for the semi-continuous exposure, with one component for exposure status (exposed vs unexposed) and another for the exposure level among those exposed, and incorporates both into a marginal structural model that disentangles the effects of exposure status and dose. The two-stage procedure sequentially targets the causal dose-response among exposed individuals and the causal effect of exposure status at a reference dose, allowing flexibility in the choice of propensity score methods in the second stage. We establish consistency and asymptotic normality for the resulting estimators, and characterise their limiting values under misspecification of the propensity score models. Simulation studies evaluate finite sample performance and robustness, and an application to a study of prenatal alcohol exposure and child cognition demonstrates how the proposed methods can be used to address a range of scientific questions about both exposure status and exposure intensity.

stat.ME