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

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dc.contributor Háskóli Íslands
dc.contributor University of Iceland
dc.contributor.author Weng, Lu-Chen
dc.contributor.author Lunetta, Kathryn L.
dc.contributor.author Müller-Nurasyid, Martina
dc.contributor.author Smith, Albert Vernon
dc.contributor.author Thériault, Sébastien
dc.contributor.author Weeke, Peter E.
dc.contributor.author Barnard, John
dc.contributor.author Bis, Joshua C.
dc.contributor.author Lyytikäinen, Leo-Pekka
dc.contributor.author Kleber, Marcus E.
dc.contributor.author Martinsson, Andreas
dc.contributor.author Lin, Henry J.
dc.contributor.author Rienstra, Michiel
dc.contributor.author Trompet, Stella
dc.contributor.author Krijthe, Bouwe P.
dc.contributor.author Dörr, Marcus
dc.contributor.author Klarin, Derek
dc.contributor.author Chasman, Daniel I.
dc.contributor.author Sinner, Moritz F.
dc.contributor.author Waldenberger, Melanie
dc.contributor.author Launer, Lenore J.
dc.contributor.author Harris, Tamara B.
dc.contributor.author Soliman, Elsayed Z.
dc.contributor.author Alonso, Alvaro
dc.contributor.author Paré, Guillaume
dc.contributor.author Teixeira, Pedro L.
dc.contributor.author Denny, Joshua C.
dc.contributor.author Shoemaker, M. Benjamin
dc.contributor.author Van Wagoner, David R.
dc.contributor.author Smith, Jonathan D.
dc.contributor.author Psaty, Bruce M.
dc.contributor.author Sotoodehnia, Nona
dc.contributor.author Taylor, Kent D.
dc.contributor.author Kähönen, Mika
dc.contributor.author Nikus, Kjell
dc.contributor.author Delgado, Graciela E.
dc.contributor.author Melander, Olle
dc.contributor.author Engström, Gunnar
dc.contributor.author Yao, Jie
dc.contributor.author Guo, Xiuqing
dc.contributor.author Christophersen, Ingrid E.
dc.contributor.author Ellinor, Patrick T.
dc.contributor.author Geelhoed, Bastiaan
dc.contributor.author Verweij, Niek
dc.contributor.author Macfarlane, Peter
dc.contributor.author Ford, Ian
dc.contributor.author Heeringa, Jan
dc.contributor.author Franco, Oscar H.
dc.contributor.author Uitterlinden, André G.
dc.contributor.author Völker, Uwe
dc.contributor.author Teumer, Alexander
dc.contributor.author Rose, Lynda M.
dc.contributor.author Kääb, Stefan
dc.contributor.author Gudnason, Vilmundur
dc.contributor.author Arking, Dan E.
dc.contributor.author Conen, David
dc.contributor.author Roden, Dan M.
dc.contributor.author Chung, Mina K.
dc.contributor.author Heckbert, Susan R.
dc.contributor.author Benjamin, Emelia J.
dc.contributor.author Lehtimäki, Terho
dc.contributor.author März, Winfried
dc.contributor.author Smith, J. Gustav
dc.contributor.author Rotter, Jerome I.
dc.contributor.author van der Harst, Pim
dc.contributor.author Jukema, J. Wouter
dc.contributor.author Stricker, Bruno H.
dc.contributor.author Felix, Stephan B.
dc.contributor.author Albert, Christine M.
dc.contributor.author Lubitz, Steven A.
dc.date.accessioned 2017-11-01T13:58:45Z
dc.date.available 2017-11-01T13:58:45Z
dc.date.issued 2017-09-12
dc.identifier.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
dc.identifier.issn 2045-2322
dc.identifier.uri https://hdl.handle.net/20.500.11815/443
dc.description.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.
dc.description.sponsorship This work is funded by the European Commision’s Horizon 2020 research and innovation programme (grant number 633196: CATCH ME to Dr. Sinner). AGES: The Age, Gene/Environment Susceptibility Reykjavik Study is funded by NIH contract N01-AG-12100. ARIC: The Atherosclerosis Risk in Communities Study is carried out as a collaborative study supported by National Heart, Lung, and Blood Institute contracts (HHSN268201100005C, HHSN268201100006C, HHSN268201100007C, HHSN268201100008C, HHSN268201100009C, HHSN268201100010C, HHSN268201100011C, and HHSN268201100012C), R01HL087641, R01HL59367 and R01HL086694; National Human Genome Research Institute contract U01HG004402; and National Institutes of Health contract HHSN268200625226C. The authors thank the staff and participants of the ARIC study for their important contributions. Infrastructure was partly supported by Grant Number UL1RR025005, a component of the National Institutes of Health and NIH Roadmap for Medical Research. This work was additionally supported by American Heart Association grant 16EIA26410001 (Alonso). BioVU: The dataset used in the analyses described were obtained from Vanderbilt University Medical Centers BioVU which is supported by institutional funding and by the Vanderbilt CTSA grant UL1 TR000445 from NCATS/NIH. Genome-wide genotyping was funded by NIH grants RC2GM092618 from NIGMS/OD and U01HG004603 from NHGRI/NIGMS. CCAF: R01 HL090620 and R01 HL111314 from the National Heart, Lung, and Blood Institute (Chung, Barnard, J. Smith, Van Wagoner); NIH/NCRR, CTSA 1UL-RR024989 (Chung, Van Wagoner); Heart and Vascular Institute, Department of Cardiovascular Medicine, Cleveland Clinic (Chung); Tomsich Atrial Fibrillation Research Fund (Chung); Leducq Foundation 07-CVD 03 (Van Wagoner, Chung); Atrial Fibrillation Innovation Center, State of Ohio (Van Wagoner, Chung). CHS: This Cardiovascular Health Study research was supported by NHLBI contracts HHSN268201200036C, HHSN268200800007C, N01HC55222, N01HC85079, N01HC85080, N01HC85081, N01HC85082, N01HC85083, N01HC85086; and NHLBI grants U01HL080295, R01HL087652, R01HL105756, R01HL103612, R01HL120393, and R01HL130114 with additional contribution from the National Institute of Neurological Disorders and Stroke (NINDS). Additional support was provided through R01AG023629 from the National Institute on Aging (NIA). A full list of principal CHS investigators and institutions can be found at CHS-NHLBI.org. The provision of genotyping data was supported in part by the National Center for Advancing Translational Sciences, CTSI grant UL1TR000124, and the National Institute of Diabetes and Digestive and Kidney Disease Diabetes Research Center (DRC) grant DK063491 to the Southern California Diabetes Endocrinology Research Center. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. Dr. Psaty serves on the DSMB of a clinical trial funded by Zoll LifeCor and on the Steering Committee of the Yale Open Data Access Project funded by Johnson & Johnson. FINCAVAS: The Finnish Cardiovascular Study (FINCAVAS) has been financially supported by the Competitive Research Funding of the Tampere University Hospital (Grant 9M048 and 9N035), the Finnish Cultural Foundation, the Finnish Foundation for Cardiovascular Research, the Emil Aaltonen Foundation, Finland, and the Tampere Tuberculosis Foundation. FHS: Funding for SHARe Affymetrix genotyping was provided by NHLBI Contract N02-HL-64278. SHARe Illumina genotyping was provided under an agreement between Illumina and Boston University. Funding support for the FHS through 1R01HL128914; 2R01 HL092577; HHSN268201500001I; N01-HC 25195; and Framingham Atrial Fibrillation/Flutter reviewed through 2012 dataset was provided by NHLBI grants 1R01HL092577, 1R01HL102214, 1RC1HL101056 and NINDS grant 6R01-NS-17950. LURIC: The Ludwigshafen Risk and Cardiovascular Health study was supported by the seventh framework program of the European commission (RiskyCAD, grant agreement number 305739). Support for genotyping was provided by the seventh framework program of the European commission (AtheroRemo, grant agreement number 201668). MESA: The Multi-Ethnic Study of Atherosclerosis study was supported by NIH contracts HHSN2682015000031, N01-HC-95159, N01-HC-95160, N01-HC-95161, N01-HC-95162, N01-HC-95163, N01-HC-95164, N01-HC-95165, N01-HC-95166, N01-HC-95167, N01-HC-95168, N01-HC-95169 and by grants UL1-TR-000040, UL1-TR-001079, and UL1-RR-025005 from NCRR. Funding for MESA SHARe genotyping was provided by NHLBI Contract N02-HL-6-4278. The provision of genotyping data was supported in part by the National Center for Advancing Translational Sciences, CTSI grant UL1TR000124, and the National Institute of Diabetes and Digestive and Kidney Disease Diabetes Research Center (DRC) grant DK063491 to the Southern California Diabetes Endocrinology Research Center. PREVEND: The PREVEND study is supported by the Dutch Kidney Foundation (grant E0.13) and the Netherlands Heart Foundation (grant NHS2010B280). Dr. M. Rienstra is supported by grants from the Netherlands Organization for Scientific Research (Veni grant 016.136.055). PROSPER: The PROSPER study was supported by an investigator initiated grant obtained from Bristol-Myers Squibb. Prof. Dr. J. W. Jukema is an Established Clinical Investigator of the Netherlands Heart Foundation (grant 2001 D 032). Support for genotyping was provided by the seventh framework program of the European commission (grant 223004) and by the Netherlands Genomics Initiative (Netherlands Consortium for Healthy Aging grant 050-060-810). RS: The Rotterdam Study is supported by the Erasmus Medical Center and Erasmus University Rotterdam; the Netherlands Organization for Scientific Research; the Netherlands Organization for Health Research and Development (ZonMw); the Research Institute for Diseases in the Elderly; The Netherlands Heart Foundation; the Ministry of Education, Culture and Science; the Ministry of Health Welfare and Sports; the European Commission; and the Municipality of Rotterdam. Support for genotyping was provided by the Netherlands Organization for Scientific Research (NWO) (175.010.2005.011, 911.03.012) and Research Institute for Diseases in the Elderly (RIDE). Oscar H. Franco works in ErasmusAGE, a center for aging research across the life course funded by Nestlé Nutrition (Nestec Ltd.), Metagenics, Inc., and AXA. Nestlé Nutrition (Nestec Ltd.), Metagenics, Inc., and AXA had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; and preparation, review, or approval of the manuscript. SHIP: SHIP is part of the Community Medicine Research net of the University of Greifswald, Germany, which is funded by the Federal Ministry of Education and Research (grants no. 01ZZ9603, 01ZZ0103, and 01ZZ0403), the Ministry of Cultural Affairs as well as the Social Ministry of the Federal State of Mecklenburg-West Pomerania, and the network ‘Greifswald Approach to Individualized Medicine (GANI_MED)’ funded by the Federal Ministry of Education and Research (grant 03IS2061A). Genome-wide data have been supported by the Federal Ministry of Education and Research (grant no. 03ZIK012) and a joint grant from Siemens Healthcare, Erlangen, Germany and the Federal State of Mecklenburg- West Pomerania. The University of Greifswald is a member of the Caché Campus program of the InterSystems GmbH.
dc.format.extent 11303
dc.language.iso en
dc.publisher Springer Nature
dc.relation info:eu-repo/grantAgreement/EC/H2020/633196
dc.relation info:eu-repo/grantAgreement/EC/FP7/305739
dc.relation info:eu-repo/grantAgreement/EC/FP7/201668
dc.relation info:eu-repo/grantAgreement/EC/FP7/223004
dc.relation.ispartofseries Scientific Reports;7(1)
dc.rights info:eu-repo/semantics/openAccess
dc.subject Cardiology
dc.subject Genome-wide association studies
dc.subject Hjartasjúkdómar
dc.subject Háþrýstingur
dc.subject Aldurshópar
dc.subject Líkamsþyngd
dc.subject Erfðafræði
dc.subject Rannsóknir
dc.title Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium
dc.type info:eu-repo/semantics/article
dcterms.license This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
dc.description.version Peer Reviewed
dc.identifier.journal Scientific Reports
dc.identifier.doi 10.1038/s41598-017-09396-7
dc.contributor.department Læknadeild (HÍ)
dc.contributor.department Faculty of Medicine (UI)
dc.contributor.school Heilbrigðisvísindasvið (HÍ)
dc.contributor.school School of Health Sciences (UI)


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