Literature DB >> 28070985

Boosting the precision of mediation analyses of randomised experiments through covariate adjustment.

S Vandenberghe1, S Vansteelandt1, T Loeys2.   

Abstract

Analyses of randomised experiments frequently include attempts to decompose the intention-to-treat effect into a direct and indirect effect, mediated by given intermediaries, with the aim to shed light onto the treatment mechanism. Methods from causal mediation analysis have facilitated this by allowing for arbitrary models for the outcome and the mediator. They thereby generalise the traditional approach to direct and indirect effects, which is essentially limited to linear models. The default maximum likelihood methods make use of a model for the conditional distribution of the mediator, given treatment and baseline covariates, but are prone to bias when that model is misspecified. In randomised experiments, specification of such model can be easily avoided, but at the expense of a sometimes major efficiency loss when those baseline covariates are predictive of the mediator. In this article, we develop a compromise approach: it makes use of a model for the mediator to optimally extract information from the baseline covariate data but is insulated from the impact of misspecification of that model; it achieves this by exploiting the known randomisation probabilities. Simulation studies and the analysis of a randomised study show major efficiency gains and confirm our theoretical findings that the default methods from causal mediation analysis are sometimes, although not always, reasonably robust to model misspecification.
Copyright © 2017 John Wiley & Sons, Ltd. Copyright © 2017 John Wiley & Sons, Ltd.

Entities:  

Keywords:  causal inference; direct effect; indirect effect; mechanism; mediated effect

Mesh:

Year:  2017        PMID: 28070985     DOI: 10.1002/sim.7219

Source DB:  PubMed          Journal:  Stat Med        ISSN: 0277-6715            Impact factor:   2.373


  3 in total

1.  Counterfactual mediation analysis in the multistate model framework for surrogate and clinical time-to-event outcomes in randomized controlled trials.

Authors:  Isabelle R Weir; Jennifer R Rider; Ludovic Trinquart
Journal:  Pharm Stat       Date:  2021-08-04       Impact factor: 1.894

2.  Mediation analysis of time-to-event endpoints accounting for repeatedly measured mediators subject to time-varying confounding.

Authors:  Stijn Vansteelandt; Martin Linder; Sjouke Vandenberghe; Johan Steen; Jesper Madsen
Journal:  Stat Med       Date:  2019-08-14       Impact factor: 2.373

3.  Beyond total treatment effects in randomised controlled trials: Baseline measurement of intermediate outcomes needed to reduce confounding in mediation investigations.

Authors:  Sabine Landau; Richard Emsley; Graham Dunn
Journal:  Clin Trials       Date:  2018-03-18       Impact factor: 2.486

  3 in total

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