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Article: Mendelian randomization: causal inference leveraging genetic data

TitleMendelian randomization: causal inference leveraging genetic data
Authors
KeywordsCausal inference
genetic data
instrumental variables
mendelian randomization
pleiotropy
Issue Date1-Jun-2024
PublisherCambridge University Press
Citation
Psychological Medicine, 2024, v. 54, n. 8, p. 1461-1474 How to Cite?
Abstract

Mendelian randomization (MR) leverages genetic information to examine the causal relationship between phenotypes allowing for the presence of unmeasured confounders. MR has been widely applied to unresolved questions in epidemiology, making use of summary statistics from genome-wide association studies on an increasing number of human traits. However, an understanding of essential concepts is necessary for the appropriate application and interpretation of MR. This review aims to provide a non-technical overview of MR and demonstrate its relevance to psychiatric research. We begin with the origins of MR and the reasons for its recent expansion, followed by an overview of its statistical methodology. We then describe the limitations of MR, and how these are being addressed by recent methodological advances. We showcase the practical use of MR in psychiatry through three illustrative examples - the connection between cannabis use and psychosis, the link between intelligence and schizophrenia, and the search for modifiable risk factors for depression. The review concludes with a discussion of the prospects of MR, focusing on the integration of multi-omics data and its extension to delineating complex causal networks.


Persistent Identifierhttp://hdl.handle.net/10722/345649
ISSN
2023 Impact Factor: 5.9
2023 SCImago Journal Rankings: 2.768

 

DC FieldValueLanguage
dc.contributor.authorChen, Lane G-
dc.contributor.authorTubbs, Justin D-
dc.contributor.authorLiu, Zipeng-
dc.contributor.authorThach, Thuan Quoc-
dc.contributor.authorSham, Pak C-
dc.date.accessioned2024-08-27T09:10:14Z-
dc.date.available2024-08-27T09:10:14Z-
dc.date.issued2024-06-01-
dc.identifier.citationPsychological Medicine, 2024, v. 54, n. 8, p. 1461-1474-
dc.identifier.issn0033-2917-
dc.identifier.urihttp://hdl.handle.net/10722/345649-
dc.description.abstract<p>Mendelian randomization (MR) leverages genetic information to examine the causal relationship between phenotypes allowing for the presence of unmeasured confounders. MR has been widely applied to unresolved questions in epidemiology, making use of summary statistics from genome-wide association studies on an increasing number of human traits. However, an understanding of essential concepts is necessary for the appropriate application and interpretation of MR. This review aims to provide a non-technical overview of MR and demonstrate its relevance to psychiatric research. We begin with the origins of MR and the reasons for its recent expansion, followed by an overview of its statistical methodology. We then describe the limitations of MR, and how these are being addressed by recent methodological advances. We showcase the practical use of MR in psychiatry through three illustrative examples - the connection between cannabis use and psychosis, the link between intelligence and schizophrenia, and the search for modifiable risk factors for depression. The review concludes with a discussion of the prospects of MR, focusing on the integration of multi-omics data and its extension to delineating complex causal networks.</p>-
dc.languageeng-
dc.publisherCambridge University Press-
dc.relation.ispartofPsychological Medicine-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectCausal inference-
dc.subjectgenetic data-
dc.subjectinstrumental variables-
dc.subjectmendelian randomization-
dc.subjectpleiotropy-
dc.titleMendelian randomization: causal inference leveraging genetic data-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1017/S0033291724000321-
dc.identifier.pmid38639006-
dc.identifier.scopuseid_2-s2.0-85191038265-
dc.identifier.volume54-
dc.identifier.issue8-
dc.identifier.spage1461-
dc.identifier.epage1474-
dc.identifier.eissn1469-8978-
dc.identifier.issnl0033-2917-

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