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Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium

Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium


Title: Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium
Author: Weng, Lu-Chen
Lunetta, Kathryn L.
Müller-Nurasyid, Martina
Smith, Albert Vernon   orcid.org/0000-0003-1942-5845
Thériault, Sébastien
Weeke, Peter E.
Barnard, John
Bis, Joshua C.
Lyytikäinen, Leo-Pekka
Kleber, Marcus E.
... 60 more authors Show all authors
Date: 2017-09-12
Language: English
Scope: 11303
University/Institute: Háskóli Íslands
University of Iceland
School: Heilbrigðisvísindasvið (HÍ)
School of Health Sciences (UI)
Department: Læknadeild (HÍ)
Faculty of Medicine (UI)
Series: Scientific Reports;7(1)
ISSN: 2045-2322
DOI: 10.1038/s41598-017-09396-7
Subject: Cardiology; Genome-wide association studies; Hjartasjúkdómar; Háþrýstingur; Aldurshópar; Líkamsþyngd; Erfðafræði; Rannsóknir
URI: https://hdl.handle.net/20.500.11815/443

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Citation:

Weng, L.-C., Lunetta, K. L., Müller-Nurasyid, M., Smith, A. V., Thériault, S., Weeke, P. E., . . . Lubitz, S. A. (2017). Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium. Scientific Reports, 7(1), 11303. doi:10.1038/s41598-017-09396-7

Abstract:

It is unclear whether genetic markers interact with risk factors to influence atrial fibrillation (AF) risk. We performed genome-wide interaction analyses between genetic variants and age, sex, hypertension, and body mass index in the AFGen Consortium. Study-specific results were combined using meta-analysis (88,383 individuals of European descent, including 7,292 with AF). Variants with nominal interaction associations in the discovery analysis were tested for association in four independent studies (131,441 individuals, including 5,722 with AF). In the discovery analysis, the AF risk associated with the minor rs6817105 allele (at the PITX2 locus) was greater among subjects ≤ 65 years of age than among those > 65 years (interaction p-value = 4.0 × 10−5). The interaction p-value exceeded genome-wide significance in combined discovery and replication analyses (interaction p-value = 1.7 × 10−8). We observed one genome-wide significant interaction with body mass index and several suggestive interactions with age, sex, and body mass index in the discovery analysis. However, none was replicated in the independent sample. Our findings suggest that the pathogenesis of AF may differ according to age in individuals of European descent, but we did not observe evidence of statistically significant genetic interactions with sex, body mass index, or hypertension on AF risk.

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