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Admixture mapping of coronary artery calcification in African Americans from the NHLBI family heart study

BACKGROUND: Coronary artery calcification (CAC) is an imaging biomarker of coronary atherosclerosis. In European Americans, genome-wide association studies (GWAS) have identified several regions associated with coronary artery disease. However, few large studies have been conducted in African Americ...

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Autores principales: Gomez, Felicia, Wang, Lihua, Abel, Haley, Zhang, Qunyuan, Province, Michael A, Borecki, Ingrid B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4417236/
https://www.ncbi.nlm.nih.gov/pubmed/25902833
http://dx.doi.org/10.1186/s12863-015-0196-x
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author Gomez, Felicia
Wang, Lihua
Abel, Haley
Zhang, Qunyuan
Province, Michael A
Borecki, Ingrid B
author_facet Gomez, Felicia
Wang, Lihua
Abel, Haley
Zhang, Qunyuan
Province, Michael A
Borecki, Ingrid B
author_sort Gomez, Felicia
collection PubMed
description BACKGROUND: Coronary artery calcification (CAC) is an imaging biomarker of coronary atherosclerosis. In European Americans, genome-wide association studies (GWAS) have identified several regions associated with coronary artery disease. However, few large studies have been conducted in African Americans. The largest meta-analysis of CAC in African Americans failed to identify genome-wide significant variants despite being powered to detect effects comparable to effects identified in European Americans. Because CAC is different in prevalence and severity in African Americans and European Americans, admixture mapping is a useful approach to identify loci missed by GWAS. RESULTS: We applied admixture mapping to the African American cohort of the Family Heart Study and identified one genome-wide significant region on chromosome 12 and three potential regions on chromosomes 6, 15, and 19 that are associated with CAC. Follow-up studies using previously reported GWAS meta-analysis data suggest that the regions identified on chromosome 6 and 15 contain variants that are possibly associated with CAC. The associated region on chromosome 6 contains the gene for BMP-6, which is expressed in vascular calcific lesions. CONCLUSIONS: Our results suggest that admixture mapping can be a useful hypothesis-generating tool to identify genomic regions that contribute to complex diseases in genetically admixed populations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12863-015-0196-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-44172362015-05-03 Admixture mapping of coronary artery calcification in African Americans from the NHLBI family heart study Gomez, Felicia Wang, Lihua Abel, Haley Zhang, Qunyuan Province, Michael A Borecki, Ingrid B BMC Genet Research Article BACKGROUND: Coronary artery calcification (CAC) is an imaging biomarker of coronary atherosclerosis. In European Americans, genome-wide association studies (GWAS) have identified several regions associated with coronary artery disease. However, few large studies have been conducted in African Americans. The largest meta-analysis of CAC in African Americans failed to identify genome-wide significant variants despite being powered to detect effects comparable to effects identified in European Americans. Because CAC is different in prevalence and severity in African Americans and European Americans, admixture mapping is a useful approach to identify loci missed by GWAS. RESULTS: We applied admixture mapping to the African American cohort of the Family Heart Study and identified one genome-wide significant region on chromosome 12 and three potential regions on chromosomes 6, 15, and 19 that are associated with CAC. Follow-up studies using previously reported GWAS meta-analysis data suggest that the regions identified on chromosome 6 and 15 contain variants that are possibly associated with CAC. The associated region on chromosome 6 contains the gene for BMP-6, which is expressed in vascular calcific lesions. CONCLUSIONS: Our results suggest that admixture mapping can be a useful hypothesis-generating tool to identify genomic regions that contribute to complex diseases in genetically admixed populations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12863-015-0196-x) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-23 /pmc/articles/PMC4417236/ /pubmed/25902833 http://dx.doi.org/10.1186/s12863-015-0196-x Text en © Gomez 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
Gomez, Felicia
Wang, Lihua
Abel, Haley
Zhang, Qunyuan
Province, Michael A
Borecki, Ingrid B
Admixture mapping of coronary artery calcification in African Americans from the NHLBI family heart study
title Admixture mapping of coronary artery calcification in African Americans from the NHLBI family heart study
title_full Admixture mapping of coronary artery calcification in African Americans from the NHLBI family heart study
title_fullStr Admixture mapping of coronary artery calcification in African Americans from the NHLBI family heart study
title_full_unstemmed Admixture mapping of coronary artery calcification in African Americans from the NHLBI family heart study
title_short Admixture mapping of coronary artery calcification in African Americans from the NHLBI family heart study
title_sort admixture mapping of coronary artery calcification in african americans from the nhlbi family heart study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4417236/
https://www.ncbi.nlm.nih.gov/pubmed/25902833
http://dx.doi.org/10.1186/s12863-015-0196-x
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