Evidence map›Paper›PMID 33287714›Full record

ArticleBMC medical research methodology2020

Overlapping-sample Mendelian randomisation with multiple exposures: a Bayesian approach.

Linyi Zou, Hui Guo, Carlo Berzuini

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Article in BMC medical research methodology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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7citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

7 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) has been widely applied to causal inference in medical research. It uses genetic variants as instrumental variables (IVs) to investigate putative causal relationship between an exposure and an outcome. Traditional MR methods have mainly focussed on a two-sample setting in which IV-exposure association study and IV-outcome association study are independent. However, it is not uncommon that participants from the two studies fully overlap (one-sample) or partly overlap (overlapping-sample).

methodsWe proposed a Bayesian method that is applicable to all the three sample settings. In essence, we converted a two- or overlapping- sample MR to a one-sample MR where data were partly unmeasured. Assume that all study individuals were drawn from the same population and unmeasured data were missing at random. Then the missing data were treated au pair with the model parameters as unknown quantities, and thus, were imputed iteratively conditioning on the observed data and estimated parameters using Markov chain Monte Carlo. We generalised our model to allow for pleiotropy and multiple exposures and assessed its performance by a number of simulations using four metrics: mean, standard deviation, coverage and power. We also compared our method with classic MR methods.

resultsIn our proposed method, higher sample overlapping rate and instrument strength led to more precise estimated causal effects with higher power. Pleiotropy had a notably negative impact on the estimates. Nevertheless, the coverages were high and our model performed well in all the sample settings overall. In comparison with classic MR, our method provided estimates with higher precision. When the true causal effects were non-zero, power of their estimates was consistently higher from our method. The performance of our method was similar to classic MR in terms of coverage.

conclusionsOur model offers the flexibility of being applicable to any of the sample settings. It is an important addition to the MR literature which has restricted to one- or two- sample scenarios. Given the nature of Bayesian inference, it can be easily extended to more complex MR analysis in medical research.

Indexed as

Mendelian Randomization AnalysisBayes TheoremCausalityHumansMonte Carlo MethodBayesian approachMendelian randomizationMissing dataMultiple exposuresOverlapping-sample

Identifiers

PMID33287714
PMCPMC7720408

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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.