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MICA*049, not MICA*009, is associated with Behçet’s disease in a Chinese population
Behçet’s disease (BD) is a multi-systemic inflammatory disease. Previous reports indicated that MICA*009 confers susceptibility to BD. MICA*049 differs from MICA*009:01, a major MICA*009 subtype, only at codon 335 in exon 6. However, the potential association of MICA*049 with BD has not been addres...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659628/ https://www.ncbi.nlm.nih.gov/pubmed/31350414 http://dx.doi.org/10.1038/s41598-019-47289-z |
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author | Zhu, Weifeng Deng, Yan Wang, Jiucun Guo, Xinjian Ding, Weifeng Chao, Jiashuo Lin, Dan Wang, Yuqin Zhou, Xiaodong |
author_facet | Zhu, Weifeng Deng, Yan Wang, Jiucun Guo, Xinjian Ding, Weifeng Chao, Jiashuo Lin, Dan Wang, Yuqin Zhou, Xiaodong |
author_sort | Zhu, Weifeng |
collection | PubMed |
description | Behçet’s disease (BD) is a multi-systemic inflammatory disease. Previous reports indicated that MICA*009 confers susceptibility to BD. MICA*049 differs from MICA*009:01, a major MICA*009 subtype, only at codon 335 in exon 6. However, the potential association of MICA*049 with BD has not been addressed. In this study, we differentiated association among MICA*049, MICA*009 and HLA-B*51 with BD. A Han Chinese cohort consisting of 41 BD patients and 197 ethnically matched controls were examined with sequencing and T-ARMS-PCR for genotyping of MICA, and ARMS-PCR for HLA-B*51. The phenotype frequency of MICA*049 (41.5% versus 8.1%, OR = 8.01, P = 1.91 × 10(−8)) and HLA-B*51 (46.3% versus 15.7%, OR = 4.62, P = 1.21 × 10(−5)) were significantly higher in BD patients than those in controls, whereas MICA*009 showed no significant difference between the two groups (17.1% versus 13.2%, OR = 1.35, P = 0.51). After stratification for the effect of HLA-B*51, MICA*049 was still associated with BD in HLA-B*51 negative patients (OR = 40.61, P = 0.02). Our results indicate that MICA*049, not MICA*009, is a risk factor to BD, and that is independent from HLA-B*51 in the Han Chinese cohort. |
format | Online Article Text |
id | pubmed-6659628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66596282019-08-01 MICA*049, not MICA*009, is associated with Behçet’s disease in a Chinese population Zhu, Weifeng Deng, Yan Wang, Jiucun Guo, Xinjian Ding, Weifeng Chao, Jiashuo Lin, Dan Wang, Yuqin Zhou, Xiaodong Sci Rep Article Behçet’s disease (BD) is a multi-systemic inflammatory disease. Previous reports indicated that MICA*009 confers susceptibility to BD. MICA*049 differs from MICA*009:01, a major MICA*009 subtype, only at codon 335 in exon 6. However, the potential association of MICA*049 with BD has not been addressed. In this study, we differentiated association among MICA*049, MICA*009 and HLA-B*51 with BD. A Han Chinese cohort consisting of 41 BD patients and 197 ethnically matched controls were examined with sequencing and T-ARMS-PCR for genotyping of MICA, and ARMS-PCR for HLA-B*51. The phenotype frequency of MICA*049 (41.5% versus 8.1%, OR = 8.01, P = 1.91 × 10(−8)) and HLA-B*51 (46.3% versus 15.7%, OR = 4.62, P = 1.21 × 10(−5)) were significantly higher in BD patients than those in controls, whereas MICA*009 showed no significant difference between the two groups (17.1% versus 13.2%, OR = 1.35, P = 0.51). After stratification for the effect of HLA-B*51, MICA*049 was still associated with BD in HLA-B*51 negative patients (OR = 40.61, P = 0.02). Our results indicate that MICA*049, not MICA*009, is a risk factor to BD, and that is independent from HLA-B*51 in the Han Chinese cohort. Nature Publishing Group UK 2019-07-26 /pmc/articles/PMC6659628/ /pubmed/31350414 http://dx.doi.org/10.1038/s41598-019-47289-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhu, Weifeng Deng, Yan Wang, Jiucun Guo, Xinjian Ding, Weifeng Chao, Jiashuo Lin, Dan Wang, Yuqin Zhou, Xiaodong MICA*049, not MICA*009, is associated with Behçet’s disease in a Chinese population |
title | MICA*049, not MICA*009, is associated with Behçet’s disease in a Chinese population |
title_full | MICA*049, not MICA*009, is associated with Behçet’s disease in a Chinese population |
title_fullStr | MICA*049, not MICA*009, is associated with Behçet’s disease in a Chinese population |
title_full_unstemmed | MICA*049, not MICA*009, is associated with Behçet’s disease in a Chinese population |
title_short | MICA*049, not MICA*009, is associated with Behçet’s disease in a Chinese population |
title_sort | mica*049, not mica*009, is associated with behçet’s disease in a chinese population |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659628/ https://www.ncbi.nlm.nih.gov/pubmed/31350414 http://dx.doi.org/10.1038/s41598-019-47289-z |
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