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Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.

TitleAssociation of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
Publication TypeJournal Article
Year of Publication2010
AuthorsSmith, NL, Felix, JF, Morrison, AC, Demissie, S, Glazer, NL, Loehr, LR, Cupples, AL, Dehghan, A, Lumley, T, Rosamond, WD, Lieb, W, Rivadeneira, F, Bis, JC, Folsom, AR, Benjamin, E, Aulchenko, YS, Haritunians, T, Couper, D, Murabito, J, Wang, YA, Stricker, BH, Gottdiener, JS, Chang, PP, Wang, TJ, Rice, KM, Hofman, A, Heckbert, SR, Fox, ER, O'Donnell, CJ, Uitterlinden, AG, Rotter, JI, Willerson, JT, Levy, D, van Duijn, CM, Psaty, BM, Witteman, JCM, Boerwinkle, E, Vasan, RS
JournalCirc Cardiovasc Genet
Volume3
Issue3
Pagination256-66
Date Published2010 Jun
ISSN1942-3268
KeywordsAfrican Americans, Aged, Aged, 80 and over, Cohort Studies, Endopeptidases, European Continental Ancestry Group, Female, Genome-Wide Association Study, Heart Failure, Humans, Incidence, Male, Middle Aged, Polymorphism, Single Nucleotide, Risk, Ubiquitin-Specific Proteases
Abstract<p><b>BACKGROUND: </b>Although genetic factors contribute to the onset of heart failure (HF), no large-scale genome-wide investigation of HF risk has been published to date. We have investigated the association of 2,478,304 single-nucleotide polymorphisms with incident HF by meta-analyzing data from 4 community-based prospective cohorts: the Atherosclerosis Risk in Communities Study, the Cardiovascular Health Study, the Framingham Heart Study, and the Rotterdam Study.</p><p><b>METHODS AND RESULTS: </b>Eligible participants for these analyses were of European or African ancestry and free of clinical HF at baseline. Each study independently conducted genome-wide scans and imputed data to the approximately 2.5 million single-nucleotide polymorphisms in HapMap. Within each study, Cox proportional hazards regression models provided age- and sex-adjusted estimates of the association between each variant and time to incident HF. Fixed-effect meta-analyses combined results for each single-nucleotide polymorphism from the 4 cohorts to produce an overall association estimate and P value. A genome-wide significance P value threshold was set a priori at 5.0x10(-7). During a mean follow-up of 11.5 years, 2526 incident HF events (12%) occurred in 20 926 European-ancestry participants. The meta-analysis identified a genome-wide significant locus at chromosomal position 15q22 (1.4x10(-8)), which was 58.8 kb from USP3. Among 2895 African-ancestry participants, 466 incident HF events (16%) occurred during a mean follow-up of 13.7 years. One genome-wide significant locus was identified at 12q14 (6.7x10(-8)), which was 6.3 kb from LRIG3.</p><p><b>CONCLUSIONS: </b>We identified 2 loci that were associated with incident HF and exceeded genome-wide significance. The findings merit replication in other community-based settings of incident HF.</p>
DOI10.1161/CIRCGENETICS.109.895763
Alternate JournalCirc Cardiovasc Genet
PubMed ID20445134
PubMed Central IDPMC3025695
Grant ListN01HC55020 / HL / NHLBI NIH HHS / United States
UL1RR025005 / RR / NCRR NIH HHS / United States
N02-HL-6-4278 / HL / NHLBI NIH HHS / United States
N01-HC-25195 / HC / NHLBI NIH HHS / United States
N01 HC055022 / HC / NHLBI NIH HHS / United States
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R01 HL087652-03 / HL / NHLBI NIH HHS / United States
UL1 RR025005 / RR / NCRR NIH HHS / United States
R01 HL093328-01 / HL / NHLBI NIH HHS / United States
U01 HL080295 / HL / NHLBI NIH HHS / United States
N01 HC075150 / HC / NHLBI NIH HHS / United States
N01-HC-55022 / HC / NHLBI NIH HHS / United States
R01 HL059367 / HL / NHLBI NIH HHS / United States
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N01-HC-55016 / HC / NHLBI NIH HHS / United States
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HHSN268200625226C / / PHS HHS / United States
U01 HG004402 / HG / NHGRI NIH HHS / United States
N01HC55022 / HL / NHLBI NIH HHS / United States
N01HC55222 / HL / NHLBI NIH HHS / United States
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2K24HL04334 / HL / NHLBI NIH HHS / United States
N01-HC-85086 / HC / NHLBI NIH HHS / United States
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U01HG004402 / HG / NHGRI NIH HHS / United States
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N01 HC-55222 / HC / NHLBI NIH HHS / United States
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M01RR00425 / RR / NCRR NIH HHS / United States
R01HL087641 / HL / NHLBI NIH HHS / United States
N01-HC-55015 / HC / NHLBI NIH HHS / United States
N01 HC055222 / HC / NHLBI NIH HHS / United States
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N01HC55019 / HL / NHLBI NIH HHS / United States
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R01 HL093328 / HL / NHLBI NIH HHS / United States
P30 DK063491-04 / DK / NIDDK NIH HHS / United States
N01HC25195 / HL / NHLBI NIH HHS / United States
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DK063491 / DK / NIDDK NIH HHS / United States
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N01-HC-55018 / HC / NHLBI NIH HHS / United States
N01HC55021 / HL / NHLBI NIH HHS / United States
R01 HL087641 / HL / NHLBI NIH HHS / United States
N01 HC045133 / HC / NHLBI NIH HHS / United States
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M01 RR000425-30S1 / RR / NCRR NIH HHS / United States
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U01 HG004402-02 / HG / NHGRI NIH HHS / United States