Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/88970
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dc.contributorDepartment of Health Technology and Informaticsen_US
dc.creatorLi, GHYen_US
dc.creatorCheung, CLen_US
dc.creatorChung, AKKen_US
dc.creatorCheung, BMYen_US
dc.creatorWong, ICKen_US
dc.creatorFok, MLYen_US
dc.creatorAu, PCMen_US
dc.creatorSham, PCen_US
dc.date.accessioned2021-01-15T07:14:28Z-
dc.date.available2021-01-15T07:14:28Z-
dc.identifier.issn0033-2917en_US
dc.identifier.urihttp://hdl.handle.net/10397/88970-
dc.language.isoenen_US
dc.publisherCambridge University Pressen_US
dc.rightsThis article has been published in a revised form in Psychological Medicine http://doi.org/10.1017/S0033291720003566. This version is free to view and download for private research and study only. Not for re-distribution or re-use. Copyright © The Author(s) 2020. Published by Cambridge University Press.en_US
dc.rightsWhen citing an Accepted Manuscript or an earlier version of an article, the Cambridge University Press requests that readers also cite the Version of Record with a DOI link. The article is subsequently published in revised form in Psychological Medicine https://dx.doi.org/10.1017/S0033291720003566.en_US
dc.subjectCardiovascular diseaseen_US
dc.subjectDepressionen_US
dc.subjectGeneticsen_US
dc.subjectMendelian randomizationen_US
dc.titleEvaluation of bi-directional causal association between depression and cardiovascular diseases: a Mendelian randomization studyen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1765en_US
dc.identifier.epage1776en_US
dc.identifier.volume52en_US
dc.identifier.issue9en_US
dc.identifier.doi10.1017/S0033291720003566en_US
dcterms.abstractBackground. Depression and cardiovascular disease (CVD) are associated with each other but their relationship remains unclear. We aim to determine whether genetic predisposition to depression are causally linked to CVD [including coronary artery disease (CAD), myocardial infarction (MI), stroke and atrial fibrillation (AF)].en_US
dcterms.abstractMethods. Using summary statistics from the largest genome-wide association studies (GWAS) or GWAS meta-analysis of depression (primary analysis: n = 500 199), broad depression (help-seeking behavior for problems with nerves, anxiety, tension or depression; secondary analysis: n = 322 580), CAD (n = 184 305), MI (n = 171 875), stroke (n = 446 696) and AF (n = 1 030 836), genetic correlation was tested between two depression phenotypes and CVD [MI, stroke and AF (not CAD as its correlation was previously confirmed)]. Causality was inferred between correlated traits by Mendelian Randomization analyses.en_US
dcterms.abstractResults. Both depression phenotypes were genetically correlated with MI (depression: rG = 0.169; p = 9.03 × 10-9; broad depression: rG = 0.123; p = 1 × 10-4) and AF (depression: rG = 0.112; p = 7.80 × 10-6; broad depression: rG = 0.126; p = 3.62 × 10-6). Genetically doubling the odds of depression was causally associated with increased risk of CAD (OR = 1.099; 95% CI 1.031-1.170; p = 0.004) and MI (OR = 1.146; 95% CI 1.070-1.228; p = 1.05 × 10-4). Adjustment for blood lipid levels/smoking status attenuated the causality between depression and CAD/MI. Null causal association was observed for CVD on depression. A similar pattern of results was observed in the secondary analysis for broad depression.en_US
dcterms.abstractConclusions. Genetic predisposition to depression may have positive causal roles on CAD/MI. Genetic susceptibility to self-awareness of mood problems may be a strong causal risk factor of CAD/MI. Blood lipid levels and smoking may potentially mediate the causal pathway. Prevention and early diagnosis of depression are important in the management of CAD/MI.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationPsychological medicine, July 2022, v. 52, no. 9, p.en_US
dcterms.isPartOfPsychological medicineen_US
dcterms.issued2022-07-
dc.identifier.scopus2-s2.0-85093535747-
dc.identifier.eissn1469-8978en_US
dc.description.validate202101 bcrcen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumbera0535-n01-
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryGreen (AAM)en_US
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