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Genome-wide association study of platelet aggregation in African Americans

BACKGROUND: We have previously shown that platelet aggregation has higher heritability in African Americans than European Americans. However, a genome-wide association study (GWAS) of platelet aggregation in African Americans has not been reported. We measured platelet aggregation in response to ara...

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Autores principales: Qayyum, Rehan, Becker, Lewis C., Becker, Diane M., Faraday, Nauder, Yanek, Lisa R., Leal, Suzanne M., Shaw, Chad, Mathias, Rasika, Suktitipat, Bhoom, Bray, Paul F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4448541/
https://www.ncbi.nlm.nih.gov/pubmed/26024889
http://dx.doi.org/10.1186/s12863-015-0217-9
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author Qayyum, Rehan
Becker, Lewis C.
Becker, Diane M.
Faraday, Nauder
Yanek, Lisa R.
Leal, Suzanne M.
Shaw, Chad
Mathias, Rasika
Suktitipat, Bhoom
Bray, Paul F.
author_facet Qayyum, Rehan
Becker, Lewis C.
Becker, Diane M.
Faraday, Nauder
Yanek, Lisa R.
Leal, Suzanne M.
Shaw, Chad
Mathias, Rasika
Suktitipat, Bhoom
Bray, Paul F.
author_sort Qayyum, Rehan
collection PubMed
description BACKGROUND: We have previously shown that platelet aggregation has higher heritability in African Americans than European Americans. However, a genome-wide association study (GWAS) of platelet aggregation in African Americans has not been reported. We measured platelet aggregation in response to arachidonic acid, ADP, collagen, or epinephrine by optical aggregometry. The discovery cohort was 825 African Americans from the GeneSTAR study. Two replication cohorts were used: 119 African Americans from the Platelet Genes and Physiology Study and 1221 European Americans from GeneSTAR. Genotyping was conducted with Illumina 1 M arrays. For each cohort, age- and sex-adjusted linear mixed models were used to test for association between each SNP and each phenotype under an additive model. RESULTS: Six SNPs were significantly associated with platelet aggregation (P < 5×10(−8)) in the discovery sample. Of these, three SNPs in three different loci were confirmed: 1) rs12041331, in PEAR1 (platelet endothelial aggregation receptor 1), replicated in both African and European Americans for collagen- and epinephrine-induced aggregation, and in European Americans for ADP-induced aggregation; 2) rs11202221, in BMPR1A (bone morphogenetic protein receptor type1A), replicated in African Americans for ADP-induced aggregation; and 3) rs6566765 replicated in European Americans for ADP-induced aggregation. The rs11202221 and rs6566765 associations with agonist-induced platelet aggregation are novel. CONCLUSIONS: In this first GWAS of agonist-induced platelet aggregation in African Americans, we discovered and replicated, novel associations of two variants with ADP-induced aggregation, and confirmed the association of a PEAR1 variant with multi-agonist-induced aggregation. Further study of these genes may provide novel insights into platelet biology. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12863-015-0217-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-44485412015-05-30 Genome-wide association study of platelet aggregation in African Americans Qayyum, Rehan Becker, Lewis C. Becker, Diane M. Faraday, Nauder Yanek, Lisa R. Leal, Suzanne M. Shaw, Chad Mathias, Rasika Suktitipat, Bhoom Bray, Paul F. BMC Genet Research Article BACKGROUND: We have previously shown that platelet aggregation has higher heritability in African Americans than European Americans. However, a genome-wide association study (GWAS) of platelet aggregation in African Americans has not been reported. We measured platelet aggregation in response to arachidonic acid, ADP, collagen, or epinephrine by optical aggregometry. The discovery cohort was 825 African Americans from the GeneSTAR study. Two replication cohorts were used: 119 African Americans from the Platelet Genes and Physiology Study and 1221 European Americans from GeneSTAR. Genotyping was conducted with Illumina 1 M arrays. For each cohort, age- and sex-adjusted linear mixed models were used to test for association between each SNP and each phenotype under an additive model. RESULTS: Six SNPs were significantly associated with platelet aggregation (P < 5×10(−8)) in the discovery sample. Of these, three SNPs in three different loci were confirmed: 1) rs12041331, in PEAR1 (platelet endothelial aggregation receptor 1), replicated in both African and European Americans for collagen- and epinephrine-induced aggregation, and in European Americans for ADP-induced aggregation; 2) rs11202221, in BMPR1A (bone morphogenetic protein receptor type1A), replicated in African Americans for ADP-induced aggregation; and 3) rs6566765 replicated in European Americans for ADP-induced aggregation. The rs11202221 and rs6566765 associations with agonist-induced platelet aggregation are novel. CONCLUSIONS: In this first GWAS of agonist-induced platelet aggregation in African Americans, we discovered and replicated, novel associations of two variants with ADP-induced aggregation, and confirmed the association of a PEAR1 variant with multi-agonist-induced aggregation. Further study of these genes may provide novel insights into platelet biology. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12863-015-0217-9) contains supplementary material, which is available to authorized users. BioMed Central 2015-05-30 /pmc/articles/PMC4448541/ /pubmed/26024889 http://dx.doi.org/10.1186/s12863-015-0217-9 Text en © Qayyum et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Qayyum, Rehan
Becker, Lewis C.
Becker, Diane M.
Faraday, Nauder
Yanek, Lisa R.
Leal, Suzanne M.
Shaw, Chad
Mathias, Rasika
Suktitipat, Bhoom
Bray, Paul F.
Genome-wide association study of platelet aggregation in African Americans
title Genome-wide association study of platelet aggregation in African Americans
title_full Genome-wide association study of platelet aggregation in African Americans
title_fullStr Genome-wide association study of platelet aggregation in African Americans
title_full_unstemmed Genome-wide association study of platelet aggregation in African Americans
title_short Genome-wide association study of platelet aggregation in African Americans
title_sort genome-wide association study of platelet aggregation in african americans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4448541/
https://www.ncbi.nlm.nih.gov/pubmed/26024889
http://dx.doi.org/10.1186/s12863-015-0217-9
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