Common Genetic Variants Associated with Sudden Cardiac Death : The FinSCDgen Study

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dc.contributor.author Lahtinen, Annukka
dc.contributor.author Noseworthy, Peter A
dc.contributor.author Havulinna, Aki S
dc.contributor.author Jula, Antti
dc.contributor.author Karhunen, Pekka J
dc.contributor.author Kettunen, Johannes
dc.contributor.author Perola, Markus
dc.contributor.author Kontula, Kimmo
dc.contributor.author Newton-Cheh, Christopher
dc.contributor.author Salomaa, Veikko
dc.date.accessioned 2012-10-03T08:21:42Z
dc.date.available 2012-10-03T08:21:42Z
dc.date.issued 2012
dc.identifier.issn 1932-6203 -
dc.identifier.uri http://tampub.uta.fi/handle/10024/66337
dc.description Public Library of Science open access -
dc.description.abstract Background Sudden cardiac death (SCD) accounts for up to half of cardiac mortality. The risk of SCD is heritable but the underlying genetic variants are largely unknown. We investigated whether common genetic variants predisposing to arrhythmia or related electrocardiographic phenotypes, including QT-interval prolongation, are associated with increased risk of SCD. Methodology/Principal Findings We studied the association between 28 candidate SNPs and SCD in a meta-analysis of four population cohorts (FINRISK 1992, 1997, 2002 and Health 2000, n = 27,629) and two forensic autopsy series (The Helsinki Sudden Death Study and The Tampere Autopsy Study, n = 694). We also studied the association between established cardiovascular risk factors and SCD. Causes of death were reviewed using registry-based health and autopsy data. Cox regression and logistic regression models were adjusted for age, sex, and geographic region. The total number of SCDs was 716. Two novel SNPs were associated with SCD: SCN5A rs41312391 (relative risk [RR] 1.27 per minor T allele, 95% CI 1.11–1.45, P = 3.4×10−4) and rs2200733 in 4q25 (RR 1.28 per minor T allele, 95% CI 1.11–1.48, P = 7.9×10−4). We also replicated the associations for 9p21 (rs2383207, RR 1.13 per G allele, 95% CI 1.01–1.26, P = 0.036), as well as for male sex, systolic blood pressure, diabetes, cigarette smoking, low physical activity, coronary heart disease, and digoxin use (P<0.05). Conclusions/Significance Two novel genetic variants, one in the cardiac sodium channel gene SCN5A and another at 4q25 previously associated with atrial fibrillation, are associated with SCD. -
dc.language.iso en -
dc.title Common Genetic Variants Associated with Sudden Cardiac Death : The FinSCDgen Study -
dc.type fi=Artikkeli aikakauslehdessä | en=Journal Article| -
dc.identifier.urn URN:NBN:fi:uta-201210031035 -
dc.identifier.doi 10.1371/journal.pone.0041675 -
dc.type.version fi=Kustantajan versio | en=Publisher's version| -
dc.subject.okm fi=Oikeuslääketiede ja muut lääketieteet | en=Forensic science and other medical sciences| -
dc.administrativeunit fi=Lääketieteen yksikkö | en=School of Medicine| -
dc.journal.title Plos ONE -
dc.journal.volume 7 -
dc.journal.number 7 -
dc.journal.volumepagerange 1-7 -
dc.journal.url http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0041675 -

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