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Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.

Authors :
Guillaume Lettre
Cameron D Palmer
Taylor Young
Kenechi G Ejebe
Hooman Allayee
Emelia J Benjamin
Franklyn Bennett
Donald W Bowden
Aravinda Chakravarti
Al Dreisbach
Deborah N Farlow
Aaron R Folsom
Myriam Fornage
Terrence Forrester
Ervin Fox
Christopher A Haiman
Jaana Hartiala
Tamara B Harris
Stanley L Hazen
Susan R Heckbert
Brian E Henderson
Joel N Hirschhorn
Brendan J Keating
Stephen B Kritchevsky
Emma Larkin
Mingyao Li
Megan E Rudock
Colin A McKenzie
James B Meigs
Yang A Meng
Tom H Mosley
Anne B Newman
Christopher H Newton-Cheh
Dina N Paltoo
George J Papanicolaou
Nick Patterson
Wendy S Post
Bruce M Psaty
Atif N Qasim
Liming Qu
Daniel J Rader
Susan Redline
Muredach P Reilly
Alexander P Reiner
Stephen S Rich
Jerome I Rotter
Yongmei Liu
Peter Shrader
David S Siscovick
W H Wilson Tang
Herman A Taylor
Russell P Tracy
Ramachandran S Vasan
Kevin M Waters
Rainford Wilks
James G Wilson
Richard R Fabsitz
Stacey B Gabriel
Sekar Kathiresan
Eric Boerwinkle
Source :
PLoS Genetics, Vol 7, Iss 2, p e1001300 (2011)
Publication Year :
2011
Publisher :
Public Library of Science (PLoS), 2011.

Abstract

Coronary heart disease (CHD) is the leading cause of mortality in African Americans. To identify common genetic polymorphisms associated with CHD and its risk factors (LDL- and HDL-cholesterol (LDL-C and HDL-C), hypertension, smoking, and type-2 diabetes) in individuals of African ancestry, we performed a genome-wide association study (GWAS) in 8,090 African Americans from five population-based cohorts. We replicated 17 loci previously associated with CHD or its risk factors in Caucasians. For five of these regions (CHD: CDKN2A/CDKN2B; HDL-C: FADS1-3, PLTP, LPL, and ABCA1), we could leverage the distinct linkage disequilibrium (LD) patterns in African Americans to identify DNA polymorphisms more strongly associated with the phenotypes than the previously reported index SNPs found in Caucasian populations. We also developed a new approach for association testing in admixed populations that uses allelic and local ancestry variation. Using this method, we discovered several loci that would have been missed using the basic allelic and global ancestry information only. Our conclusions suggest that no major loci uniquely explain the high prevalence of CHD in African Americans. Our project has developed resources and methods that address both admixture- and SNP-association to maximize power for genetic discovery in even larger African-American consortia.

Subjects

Subjects :
Genetics
QH426-470

Details

Language :
English
ISSN :
15537390 and 15537404
Volume :
7
Issue :
2
Database :
Directory of Open Access Journals
Journal :
PLoS Genetics
Publication Type :
Academic Journal
Accession number :
edsdoj.9f44e2061144ffba888d0850b646b15
Document Type :
article
Full Text :
https://doi.org/10.1371/journal.pgen.1001300