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A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans

African Americans are disproportionately affected by type 2 diabetes (T2DM) yet few studies have examined T2DM using genome-wide association approaches in this ethnicity. The aim of this study was to identify genes associated with T2DM in the African American population. We performed a Genome Wide A...

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Autores principales: Palmer, Nicholette D., McDonough, Caitrin W., Hicks, Pamela J., Roh, Bong H., Wing, Maria R., An, S. Sandy, Hester, Jessica M., Cooke, Jessica N., Bostrom, Meredith A., Rudock, Megan E., Talbert, Matthew E., Lewis, Joshua P., Ferrara, Assiamira, Lu, Lingyi, Ziegler, Julie T., Sale, Michele M., Divers, Jasmin, Shriner, Daniel, Adeyemo, Adebowale, Rotimi, Charles N., Ng, Maggie C. Y., Langefeld, Carl D., Freedman, Barry I., Bowden, Donald W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3251563/
https://www.ncbi.nlm.nih.gov/pubmed/22238593
http://dx.doi.org/10.1371/journal.pone.0029202
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author Palmer, Nicholette D.
McDonough, Caitrin W.
Hicks, Pamela J.
Roh, Bong H.
Wing, Maria R.
An, S. Sandy
Hester, Jessica M.
Cooke, Jessica N.
Bostrom, Meredith A.
Rudock, Megan E.
Talbert, Matthew E.
Lewis, Joshua P.
Ferrara, Assiamira
Lu, Lingyi
Ziegler, Julie T.
Sale, Michele M.
Divers, Jasmin
Shriner, Daniel
Adeyemo, Adebowale
Rotimi, Charles N.
Ng, Maggie C. Y.
Langefeld, Carl D.
Freedman, Barry I.
Bowden, Donald W.
author_facet Palmer, Nicholette D.
McDonough, Caitrin W.
Hicks, Pamela J.
Roh, Bong H.
Wing, Maria R.
An, S. Sandy
Hester, Jessica M.
Cooke, Jessica N.
Bostrom, Meredith A.
Rudock, Megan E.
Talbert, Matthew E.
Lewis, Joshua P.
Ferrara, Assiamira
Lu, Lingyi
Ziegler, Julie T.
Sale, Michele M.
Divers, Jasmin
Shriner, Daniel
Adeyemo, Adebowale
Rotimi, Charles N.
Ng, Maggie C. Y.
Langefeld, Carl D.
Freedman, Barry I.
Bowden, Donald W.
author_sort Palmer, Nicholette D.
collection PubMed
description African Americans are disproportionately affected by type 2 diabetes (T2DM) yet few studies have examined T2DM using genome-wide association approaches in this ethnicity. The aim of this study was to identify genes associated with T2DM in the African American population. We performed a Genome Wide Association Study (GWAS) using the Affymetrix 6.0 array in 965 African-American cases with T2DM and end-stage renal disease (T2DM-ESRD) and 1029 population-based controls. The most significant SNPs (n = 550 independent loci) were genotyped in a replication cohort and 122 SNPs (n = 98 independent loci) were further tested through genotyping three additional validation cohorts followed by meta-analysis in all five cohorts totaling 3,132 cases and 3,317 controls. Twelve SNPs had evidence of association in the GWAS (P<0.0071), were directionally consistent in the Replication cohort and were associated with T2DM in subjects without nephropathy (P<0.05). Meta-analysis in all cases and controls revealed a single SNP reaching genome-wide significance (P<2.5×10(−8)). SNP rs7560163 (P = 7.0×10(−9), OR (95% CI) = 0.75 (0.67–0.84)) is located intergenically between RND3 and RBM43. Four additional loci (rs7542900, rs4659485, rs2722769 and rs7107217) were associated with T2DM (P<0.05) and reached more nominal levels of significance (P<2.5×10(−5)) in the overall analysis and may represent novel loci that contribute to T2DM. We have identified novel T2DM-susceptibility variants in the African-American population. Notably, T2DM risk was associated with the major allele and implies an interesting genetic architecture in this population. These results suggest that multiple loci underlie T2DM susceptibility in the African-American population and that these loci are distinct from those identified in other ethnic populations.
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spelling pubmed-32515632012-01-11 A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans Palmer, Nicholette D. McDonough, Caitrin W. Hicks, Pamela J. Roh, Bong H. Wing, Maria R. An, S. Sandy Hester, Jessica M. Cooke, Jessica N. Bostrom, Meredith A. Rudock, Megan E. Talbert, Matthew E. Lewis, Joshua P. Ferrara, Assiamira Lu, Lingyi Ziegler, Julie T. Sale, Michele M. Divers, Jasmin Shriner, Daniel Adeyemo, Adebowale Rotimi, Charles N. Ng, Maggie C. Y. Langefeld, Carl D. Freedman, Barry I. Bowden, Donald W. PLoS One Research Article African Americans are disproportionately affected by type 2 diabetes (T2DM) yet few studies have examined T2DM using genome-wide association approaches in this ethnicity. The aim of this study was to identify genes associated with T2DM in the African American population. We performed a Genome Wide Association Study (GWAS) using the Affymetrix 6.0 array in 965 African-American cases with T2DM and end-stage renal disease (T2DM-ESRD) and 1029 population-based controls. The most significant SNPs (n = 550 independent loci) were genotyped in a replication cohort and 122 SNPs (n = 98 independent loci) were further tested through genotyping three additional validation cohorts followed by meta-analysis in all five cohorts totaling 3,132 cases and 3,317 controls. Twelve SNPs had evidence of association in the GWAS (P<0.0071), were directionally consistent in the Replication cohort and were associated with T2DM in subjects without nephropathy (P<0.05). Meta-analysis in all cases and controls revealed a single SNP reaching genome-wide significance (P<2.5×10(−8)). SNP rs7560163 (P = 7.0×10(−9), OR (95% CI) = 0.75 (0.67–0.84)) is located intergenically between RND3 and RBM43. Four additional loci (rs7542900, rs4659485, rs2722769 and rs7107217) were associated with T2DM (P<0.05) and reached more nominal levels of significance (P<2.5×10(−5)) in the overall analysis and may represent novel loci that contribute to T2DM. We have identified novel T2DM-susceptibility variants in the African-American population. Notably, T2DM risk was associated with the major allele and implies an interesting genetic architecture in this population. These results suggest that multiple loci underlie T2DM susceptibility in the African-American population and that these loci are distinct from those identified in other ethnic populations. Public Library of Science 2012-01-04 /pmc/articles/PMC3251563/ /pubmed/22238593 http://dx.doi.org/10.1371/journal.pone.0029202 Text en This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Palmer, Nicholette D.
McDonough, Caitrin W.
Hicks, Pamela J.
Roh, Bong H.
Wing, Maria R.
An, S. Sandy
Hester, Jessica M.
Cooke, Jessica N.
Bostrom, Meredith A.
Rudock, Megan E.
Talbert, Matthew E.
Lewis, Joshua P.
Ferrara, Assiamira
Lu, Lingyi
Ziegler, Julie T.
Sale, Michele M.
Divers, Jasmin
Shriner, Daniel
Adeyemo, Adebowale
Rotimi, Charles N.
Ng, Maggie C. Y.
Langefeld, Carl D.
Freedman, Barry I.
Bowden, Donald W.
A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans
title A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans
title_full A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans
title_fullStr A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans
title_full_unstemmed A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans
title_short A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans
title_sort genome-wide association search for type 2 diabetes genes in african americans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3251563/
https://www.ncbi.nlm.nih.gov/pubmed/22238593
http://dx.doi.org/10.1371/journal.pone.0029202
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