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Comprehensive Genotyping in Two Homogeneous Graves' Disease Samples Reveals Major and Novel HLA Association Alleles
BACKGROUND: Graves' disease (GD) is the leading cause of hyperthyroidism and thyroid eye disease inherited as a complex trait. Although geoepidemiology studies showed relatively higher prevalence of GD in Asians than in Caucasians, previous genetic studies were contradictory concerning whether...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3030609/ https://www.ncbi.nlm.nih.gov/pubmed/21307958 http://dx.doi.org/10.1371/journal.pone.0016635 |
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author | Chen, Pei-Lung Fann, Cathy Shen-Jang Chu, Chen-Chung Chang, Chien-Ching Chang, Su-Wei Hsieh, Hsin-Yi Lin, Marie Yang, Wei-Shiung Chang, Tien-Chun |
author_facet | Chen, Pei-Lung Fann, Cathy Shen-Jang Chu, Chen-Chung Chang, Chien-Ching Chang, Su-Wei Hsieh, Hsin-Yi Lin, Marie Yang, Wei-Shiung Chang, Tien-Chun |
author_sort | Chen, Pei-Lung |
collection | PubMed |
description | BACKGROUND: Graves' disease (GD) is the leading cause of hyperthyroidism and thyroid eye disease inherited as a complex trait. Although geoepidemiology studies showed relatively higher prevalence of GD in Asians than in Caucasians, previous genetic studies were contradictory concerning whether and/or which human leukocyte antigen (HLA) alleles are associated with GD in Asians. METHODOLOGY/PRINCIPAL FINDINGS: We conducted a case-control association study (499 unrelated GD cases and 504 controls) and a replication in an independent family sample (419 GD individuals and their 282 relatives in 165 families). To minimize genetic and phenotypic heterogeneity, we included only ethnic Chinese Han population in Taiwan and excluded subjects with hypothyroidism. We performed direct and comprehensive genotyping of six classical HLA loci (HLA-A, -B, -C, -DPB1, -DQB1 and -DRB1) to 4-digit resolution. Combining the data of two sample populations, we found that B*46:01 (odds ratio under dominant model [OR] = 1.33, Bonferroni corrected combined P [P(Bc)] = 1.17×10(−2)), DPB1*05:01 (OR = 2.34, P(Bc) = 2.58×10(−10)), DQB1*03:02 (OR = 0.62, P(Bc) = 1.97×10(−2)), DRB1*15:01 (OR = 1.68, P(Bc) = 1.22×10(−2)) and DRB1*16:02 (OR = 2.63, P(Bc) = 1.46×10(−5)) were associated with GD. HLA-DPB1*05:01 is the major gene of GD in our population and singly accounts for 48.4% of population-attributable risk. CONCLUSIONS/SIGNIFICANCE: These GD-associated alleles we identified in ethnic Chinese Hans, and those identified in other Asian studies, are totally distinct from the known associated alleles in Caucasians. Identification of population-specific association alleles is the critical first step for individualized medicine. Furthermore, comparison between different susceptibility/protective alleles across populations could facilitate generation of novel hypothesis about GD pathophysiology and indicate a new direction for future investigation. |
format | Text |
id | pubmed-3030609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30306092011-02-09 Comprehensive Genotyping in Two Homogeneous Graves' Disease Samples Reveals Major and Novel HLA Association Alleles Chen, Pei-Lung Fann, Cathy Shen-Jang Chu, Chen-Chung Chang, Chien-Ching Chang, Su-Wei Hsieh, Hsin-Yi Lin, Marie Yang, Wei-Shiung Chang, Tien-Chun PLoS One Research Article BACKGROUND: Graves' disease (GD) is the leading cause of hyperthyroidism and thyroid eye disease inherited as a complex trait. Although geoepidemiology studies showed relatively higher prevalence of GD in Asians than in Caucasians, previous genetic studies were contradictory concerning whether and/or which human leukocyte antigen (HLA) alleles are associated with GD in Asians. METHODOLOGY/PRINCIPAL FINDINGS: We conducted a case-control association study (499 unrelated GD cases and 504 controls) and a replication in an independent family sample (419 GD individuals and their 282 relatives in 165 families). To minimize genetic and phenotypic heterogeneity, we included only ethnic Chinese Han population in Taiwan and excluded subjects with hypothyroidism. We performed direct and comprehensive genotyping of six classical HLA loci (HLA-A, -B, -C, -DPB1, -DQB1 and -DRB1) to 4-digit resolution. Combining the data of two sample populations, we found that B*46:01 (odds ratio under dominant model [OR] = 1.33, Bonferroni corrected combined P [P(Bc)] = 1.17×10(−2)), DPB1*05:01 (OR = 2.34, P(Bc) = 2.58×10(−10)), DQB1*03:02 (OR = 0.62, P(Bc) = 1.97×10(−2)), DRB1*15:01 (OR = 1.68, P(Bc) = 1.22×10(−2)) and DRB1*16:02 (OR = 2.63, P(Bc) = 1.46×10(−5)) were associated with GD. HLA-DPB1*05:01 is the major gene of GD in our population and singly accounts for 48.4% of population-attributable risk. CONCLUSIONS/SIGNIFICANCE: These GD-associated alleles we identified in ethnic Chinese Hans, and those identified in other Asian studies, are totally distinct from the known associated alleles in Caucasians. Identification of population-specific association alleles is the critical first step for individualized medicine. Furthermore, comparison between different susceptibility/protective alleles across populations could facilitate generation of novel hypothesis about GD pathophysiology and indicate a new direction for future investigation. Public Library of Science 2011-01-28 /pmc/articles/PMC3030609/ /pubmed/21307958 http://dx.doi.org/10.1371/journal.pone.0016635 Text en Chen et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Chen, Pei-Lung Fann, Cathy Shen-Jang Chu, Chen-Chung Chang, Chien-Ching Chang, Su-Wei Hsieh, Hsin-Yi Lin, Marie Yang, Wei-Shiung Chang, Tien-Chun Comprehensive Genotyping in Two Homogeneous Graves' Disease Samples Reveals Major and Novel HLA Association Alleles |
title | Comprehensive Genotyping in Two Homogeneous Graves' Disease Samples Reveals Major and Novel HLA Association Alleles |
title_full | Comprehensive Genotyping in Two Homogeneous Graves' Disease Samples Reveals Major and Novel HLA Association Alleles |
title_fullStr | Comprehensive Genotyping in Two Homogeneous Graves' Disease Samples Reveals Major and Novel HLA Association Alleles |
title_full_unstemmed | Comprehensive Genotyping in Two Homogeneous Graves' Disease Samples Reveals Major and Novel HLA Association Alleles |
title_short | Comprehensive Genotyping in Two Homogeneous Graves' Disease Samples Reveals Major and Novel HLA Association Alleles |
title_sort | comprehensive genotyping in two homogeneous graves' disease samples reveals major and novel hla association alleles |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3030609/ https://www.ncbi.nlm.nih.gov/pubmed/21307958 http://dx.doi.org/10.1371/journal.pone.0016635 |
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