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Genome-Wide Association Study of Coronary Artery Disease

Coronary artery disease (CAD) is a multifactorial disease with environmental and genetic determinants. The genetic determinants of CAD have previously been explored by the candidate gene approach. Recently, the data from the International HapMap Project and the development of dense genotyping chips...

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Detalles Bibliográficos
Autores principales: Ogawa, Naomi, Imai, Yasushi, Morita, Hiroyuki, Nagai, Ryozo
Formato: Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2958466/
https://www.ncbi.nlm.nih.gov/pubmed/20981302
http://dx.doi.org/10.4061/2010/790539
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author Ogawa, Naomi
Imai, Yasushi
Morita, Hiroyuki
Nagai, Ryozo
author_facet Ogawa, Naomi
Imai, Yasushi
Morita, Hiroyuki
Nagai, Ryozo
author_sort Ogawa, Naomi
collection PubMed
description Coronary artery disease (CAD) is a multifactorial disease with environmental and genetic determinants. The genetic determinants of CAD have previously been explored by the candidate gene approach. Recently, the data from the International HapMap Project and the development of dense genotyping chips have enabled us to perform genome-wide association studies (GWAS) on a large number of subjects without bias towards any particular candidate genes. In 2007, three chip-based GWAS simultaneously revealed the significant association between common variants on chromosome 9p21 and CAD. This association was replicated among other ethnic groups and also in a meta-analysis. Further investigations have detected several other candidate loci associated with CAD. The chip-based GWAS approach has identified novel and unbiased genetic determinants of CAD and these insights provide the important direction to better understand the pathogenesis of CAD and to develop new and improved preventive measures and treatments for CAD.
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spelling pubmed-29584662010-10-27 Genome-Wide Association Study of Coronary Artery Disease Ogawa, Naomi Imai, Yasushi Morita, Hiroyuki Nagai, Ryozo Int J Hypertens Review Article Coronary artery disease (CAD) is a multifactorial disease with environmental and genetic determinants. The genetic determinants of CAD have previously been explored by the candidate gene approach. Recently, the data from the International HapMap Project and the development of dense genotyping chips have enabled us to perform genome-wide association studies (GWAS) on a large number of subjects without bias towards any particular candidate genes. In 2007, three chip-based GWAS simultaneously revealed the significant association between common variants on chromosome 9p21 and CAD. This association was replicated among other ethnic groups and also in a meta-analysis. Further investigations have detected several other candidate loci associated with CAD. The chip-based GWAS approach has identified novel and unbiased genetic determinants of CAD and these insights provide the important direction to better understand the pathogenesis of CAD and to develop new and improved preventive measures and treatments for CAD. SAGE-Hindawi Access to Research 2010-09-21 /pmc/articles/PMC2958466/ /pubmed/20981302 http://dx.doi.org/10.4061/2010/790539 Text en Copyright © 2010 Naomi Ogawa et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Ogawa, Naomi
Imai, Yasushi
Morita, Hiroyuki
Nagai, Ryozo
Genome-Wide Association Study of Coronary Artery Disease
title Genome-Wide Association Study of Coronary Artery Disease
title_full Genome-Wide Association Study of Coronary Artery Disease
title_fullStr Genome-Wide Association Study of Coronary Artery Disease
title_full_unstemmed Genome-Wide Association Study of Coronary Artery Disease
title_short Genome-Wide Association Study of Coronary Artery Disease
title_sort genome-wide association study of coronary artery disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2958466/
https://www.ncbi.nlm.nih.gov/pubmed/20981302
http://dx.doi.org/10.4061/2010/790539
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