Title | Genome-wide association analysis of incident coronary heart disease (CHD) in African Americans: a short report. |
Publication Type | Journal Article |
Year of Publication | 2011 |
Authors | Barbalic, M, Reiner, AP, Wu, C, Hixson, JE, Franceschini, N, Eaton, CB, Heiss, G, Couper, D, Mosley, T, Boerwinkle, E |
Journal | PLoS Genet |
Volume | 7 |
Issue | 8 |
Pagination | e1002199 |
Date Published | 2011 Aug |
ISSN | 1553-7404 |
Keywords | Aged, Black or African American, Coronary Disease, Female, Gene Expression Regulation, Genetic Loci, Genome-Wide Association Study, Humans, Male, Middle Aged, Polymorphism, Single Nucleotide, Risk Factors |
Abstract | African Americans have the highest rate of mortality due to coronary heart disease (CHD). Although multiple loci have been identified influencing CHD risk in European-Americans using a genome-wide association (GWAS) approach, no GWAS of incident CHD has been reported for African Americans. We performed a GWAS for incident CHD events collected during 19 years of follow-up in 2,905 African Americans from the Atherosclerosis Risk in Communities (ARIC) study. We identified a genome-wide significant SNP (rs1859023, MAF = 31%) located at 7q21 near the PFTK1 gene (HR = 0.57, 95% CI 0.46 to 0.69, p = 1.86×10(-08)), which replicated in an independent sample of over 8,000 African American women from the Women's Health Initiative (WHI) (HR = 0.81, 95% CI 0.70 to 0.93, p = 0.005). PFTK1 encodes a serine/threonine-protein kinase, PFTAIRE-1, that acts as a cyclin-dependent kinase regulating cell cycle progression and cell proliferation. This is the first finding of incident CHD locus identified by GWAS in African Americans. |
DOI | 10.1371/journal.pgen.1002199 |
Alternate Journal | PLoS Genet |
PubMed ID | 21829389 |
PubMed Central ID | PMC3150445 |
Grant List | R01 HL059367 / HL / NHLBI NIH HHS / United States HHSN268201100007C / HL / NHLBI NIH HHS / United States 32100-2 / / PHS HHS / United States R01HL087641 / HL / NHLBI NIH HHS / United States HHSN268201100005I / HL / NHLBI NIH HHS / United States 32118-32119 / / PHS HHS / United States 32108-9 / / PHS HHS / United States HHSN268201100007I / HL / NHLBI NIH HHS / United States 32122 / / PHS HHS / United States R01 HL087641 / HL / NHLBI NIH HHS / United States 44221 / / PHS HHS / United States 32111-13 / / PHS HHS / United States N01WH22110 / WH / WHI NIH HHS / United States R01HL086694 / HL / NHLBI NIH HHS / United States HHSN268201100012C / HL / NHLBI NIH HHS / United States UL1RR025005 / RR / NCRR NIH HHS / United States HHSN268201100009I / HL / NHLBI NIH HHS / United States 32105-6 / / PHS HHS / United States R01HL59367 / HL / NHLBI NIH HHS / United States HHSN268201100010C / HL / NHLBI NIH HHS / United States UL1 RR025005 / RR / NCRR NIH HHS / United States HHSN268201100008C / HL / NHLBI NIH HHS / United States HHSN268201100005G / HL / NHLBI NIH HHS / United States HHSN268201100008I / HL / NHLBI NIH HHS / United States 42107-26 / / PHS HHS / United States 32115 / / PHS HHS / United States HHSN268201100011I / HL / NHLBI NIH HHS / United States HHSN268201100011C / HL / NHLBI NIH HHS / United States R01 HL086694 / HL / NHLBI NIH HHS / United States HHSN268200625226C / / PHS HHS / United States U01 HG004402 / HG / NHGRI NIH HHS / United States 24152 / / PHS HHS / United States U01HG004402 / HG / NHGRI NIH HHS / United States HHSN268201100006C / HL / NHLBI NIH HHS / United States 42129-32 / / PHS HHS / United States HHSN268201100009C / HL / NHLBI NIH HHS / United States HHSN268201100005C / HL / NHLBI NIH HHS / United States |
Genome-wide association analysis of incident coronary heart disease (CHD) in African Americans: a short report.
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