Evidence map›Paper›PMID 35658839›Full record

ArticleBMC medical research methodology2022

Bayesian mendelian randomization with study heterogeneity and data partitioning for large studies.

Linyi Zou, Hui Guo, Carlo Berzuini

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Article in BMC medical research methodology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

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9citing papers in PubMed
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1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Linyi ZouCentre for Biostatistics, School of Health Sciences, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
Hui GuoCentre for Biostatistics, School of Health Sciences, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK. hui.guo@manchester.ac.uk.
Carlo BerzuiniCentre for Biostatistics, School of Health Sciences, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMendelian randomization (MR) is a useful approach to causal inference from observational studies when randomised controlled trials are not feasible. However, study heterogeneity of two association studies required in MR is often overlooked. When dealing with large studies, recently developed Bayesian MR can be computationally challenging, and sometimes even prohibitive.

methodsWe addressed study heterogeneity by proposing a random effect Bayesian MR model with multiple exposures and outcomes. For large studies, we adopted a subset posterior aggregation method to overcome the problem of computational expensiveness of Markov chain Monte Carlo. In particular, we divided data into subsets and combined estimated causal effects obtained from the subsets. The performance of our method was evaluated by a number of simulations, in which exposure data was partly missing.

resultsRandom effect Bayesian MR outperformed conventional inverse-variance weighted estimation, whether the true causal effects were zero or non-zero. Data partitioning of large studies had little impact on variations of the estimated causal effects, whereas it notably affected unbiasedness of the estimates with weak instruments and high missing rate of data. For the cases being simulated in our study, the results have indicated that the "divide (data) and combine (estimated subset causal effects)" can help improve computational efficiency, for an acceptable cost in terms of bias in the causal effect estimates, as long as the size of the subsets is reasonably large.

conclusionsWe further elaborated our Bayesian MR method to explicitly account for study heterogeneity. We also adopted a subset posterior aggregation method to ease computational burden, which is important especially when dealing with large studies. Despite the simplicity of the model we have used in the simulations, we hope the present work would effectively point to MR studies that allow modelling flexibility, especially in relation to the integration of heterogeneous studies and computational practicality.

Indexed as

Genome-Wide Association StudyMendelian Randomization AnalysisBayes TheoremBiasCausalityHumansMonte Carlo MethodBayesian inferenceData partitioningMendelian randomizationStudy heterogeneity

Identifiers

PMID35658839
PMCPMC9164425

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.