Causally interpretable meta-analysis combining aggregate and individual participant data

Recent work in causally-interpretable meta-analysis (CIMA) has bridged the gap between traditional meta-analysis and causal inference. While traditional meta-analysis results generally do not apply to any well-defined population, CIMA approaches specify a target population to which meta-analytic treatment effect estimates are transported. While theoretically attractive, these approaches currently have some practical limitations. Most assume that all studies in the meta-analysis have individual participant data (IPD), which is rare in practice because most trials share only aggregate data. We propose a method to perform CIMA using a combination of aggregate data and IPD. This method borrows information from studies with IPD to augment the aggregate data and create aggregate-matched synthetic IPD (AMSIPD), which can be used readily in the existing CIMA framework. By allowing use of both aggregate data and IPD, the method opens CIMA to more applications and can avoid biases arising from using only studies with IPD. We present a case study and simulations showing the AMSIPD approach is promising and merits further investigation as an advancement of CIMA.

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Publication Details

Journal
American Journal of Epidemiology
Published
2024-09-20
DOI
https://doi.org/10.1093/aje/kwae371
Citations
1
Primary Topic
Meta-analysis and systematic reviews
Type
article
Field-Weighted Citation Impact
0.46

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article

Causally interpretable meta-analysis combining aggregate and individual participant data

James S. Hodges, Justin Clark, Mohammad Hassan Murad, Jared D. Huling et al.
1 citations
American Journal of Epidemiology
Meta-analysis and systematic reviews
0.46
article

Causally interpretable meta-analysis combining aggregate and individual participant data

James S. Hodges, Justin Clark, Mohammad Hassan Murad, Jared D. Huling, Kollin W. Rott
article en
1 citations

Abstract

Recent work in causally-interpretable meta-analysis (CIMA) has bridged the gap between traditional meta-analysis and causal inference. While traditional meta-analysis results generally do not apply to any well-defined population, CIMA approaches specify a target population to which meta-analytic treatment effect estimates are transported. While theoretically attractive, these approaches currently have some practical limitations. Most assume that all studies in the meta-analysis have individual participant data (IPD), which is rare in practice because most trials share only aggregate data. We propose a method to perform CIMA using a combination of aggregate data and IPD. This method borrows information from studies with IPD to augment the aggregate data and create aggregate-matched synthetic IPD (AMSIPD), which can be used readily in the existing CIMA framework. By allowing use of both aggregate data and IPD, the method opens CIMA to more applications and can avoid biases arising from using only studies with IPD. We present a case study and simulations showing the AMSIPD approach is promising and merits further investigation as an advancement of CIMA.

American Journal of EpidemiologyVol. 194(7)
University of Minnesota (US), Mayo Clinic (US), Mayo Clinic in Arizona (US), Mayo Clinic in Florida (US)
University of Minnesota
Openalex Percentile: Top 28%
Meta-analysis and systematic reviews
0.46
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