JOM KITA KE POLITEKNIK

Statistical methods for cis‐Mendelian randomization with two‐sample summary‐level data (Record no. 946)

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Personal name Gkatzionis, Apostolos
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9 (RLIN) 2686
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Title Statistical methods for cis‐Mendelian randomization with two‐sample summary‐level data
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Name of publisher, distributor, etc. John Wiley and Sons Inc.,
Date of publication, distribution, etc. 2022-10-23.
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General note /pmc/articles/PMC7614127/
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General note /pubmed/36273411
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Summary, etc. Mendelian randomization (MR) is the use of genetic variants to assess the existence of a causal relationship between a risk factor and an outcome of interest. Here, we focus on two‐sample summary‐data MR analyses with many correlated variants from a single gene region, particularly on cis‐MR studies which use protein expression as a risk factor. Such studies must rely on a small, curated set of variants from the studied region; using all variants in the region requires inverting an ill‐conditioned genetic correlation matrix and results in numerically unstable causal effect estimates. We review methods for variable selection and estimation in cis‐MR with summary‐level data, ranging from stepwise pruning and conditional analysis to principal components analysis, factor analysis, and Bayesian variable selection. In a simulation study, we show that the various methods have comparable performance in analyses with large sample sizes and strong genetic instruments. However, when weak instrument bias is suspected, factor analysis and Bayesian variable selection produce more reliable inferences than simple pruning approaches, which are often used in practice. We conclude by examining two case studies, assessing the effects of low‐density lipoprotein‐cholesterol and serum testosterone on coronary heart disease risk using variants in the HMGCR and SHBG gene regions, respectively.
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Terms governing use and reproduction © 2022 The Authors. Genetic Epidemiology published by Wiley Periodicals LLC.
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Terms governing use and reproduction https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
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Language note en
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Topical term or geographic name as entry element Research Articles
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Genre/form data or focus term Text
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Personal name Burgess, Stephen
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Personal name Newcombe, Paul J.
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9 (RLIN) 2687
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Note Genet Epidemiol
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Uniform Resource Identifier <a href="http://dx.doi.org/10.1002/gepi.22506">http://dx.doi.org/10.1002/gepi.22506</a>
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