Cargando…

Human Leukocyte Antigen Fine-Mapping and Correlation Analysis of Han and Minority Leprosy Patients in Southern China

Backround: Leprosy is very prevalent in many populations around the world, which is well known that both alleles for human leukocyte antigen (HLA) as well as single nucleotide polymorphisms (SNPs) in the HLA region are common in leprosy patients. Previous studies have identified leprosy-associated s...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Zhuo, Wang, Yirui, Fan, Wencheng, Zhang, Chang, Liu, Hao, Zhang, Ruixue, Cao, Lu, Zhen, Qi, Chen, Weiwei, Yu, Yafen, Li, Bao, Mao, Yiwen, Bai, Yuanming, Wang, Daiyue, Luo, Sihan, Li, Yuanyuan, Qin, Qin, Ge, Huiyao, Yong, Liang, Hu, Xia, Yu, Yanxia, Sun, Liangdan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234480/
https://www.ncbi.nlm.nih.gov/pubmed/35769990
http://dx.doi.org/10.3389/fgene.2022.888361
_version_ 1784736085993062400
author Li, Zhuo
Wang, Yirui
Fan, Wencheng
Zhang, Chang
Liu, Hao
Zhang, Ruixue
Cao, Lu
Zhen, Qi
Chen, Weiwei
Yu, Yafen
Li, Bao
Mao, Yiwen
Bai, Yuanming
Wang, Daiyue
Luo, Sihan
Li, Yuanyuan
Qin, Qin
Ge, Huiyao
Yong, Liang
Hu, Xia
Yu, Yanxia
Sun, Liangdan
author_facet Li, Zhuo
Wang, Yirui
Fan, Wencheng
Zhang, Chang
Liu, Hao
Zhang, Ruixue
Cao, Lu
Zhen, Qi
Chen, Weiwei
Yu, Yafen
Li, Bao
Mao, Yiwen
Bai, Yuanming
Wang, Daiyue
Luo, Sihan
Li, Yuanyuan
Qin, Qin
Ge, Huiyao
Yong, Liang
Hu, Xia
Yu, Yanxia
Sun, Liangdan
author_sort Li, Zhuo
collection PubMed
description Backround: Leprosy is very prevalent in many populations around the world, which is well known that both alleles for human leukocyte antigen (HLA) as well as single nucleotide polymorphisms (SNPs) in the HLA region are common in leprosy patients. Previous studies have identified leprosy-associated susceptibility genes that explain only part of disease risk and heritability. In view of the complicated characteristics of the major histocompatibility complex (MHC) region, this study aimed to explore the development and variation of HLA in leprosy and its possible mechanism. Methods: Previous genome-wide association data were extracted from Han and minority populations in southern China for HLA fine-mapping studies. Insertion and deletion (INDEL), SNP, and copy number variation (CNV) imputation were determined by using the Thousand People Database (1KGP Phase 3 Dataset) as a reference panel. The HAN-MHC database was used to input the HLA classical alleles and amino acids in the MHC region, and further step-regression analysis was performed to analyze independent variation signals associated with leprosy. Results: The most significant locus rs75324027 (the same locus as rs602875 in the HLA-DR region) [p = 7.49E-09, OR= 0.62, 95%,CI: 0.52–0.73] in the intergene region between HLA-DQA1 and HLA-DRB1 was related with leprosy in M-S(Han leprosy patients in south China)disease. In M-SM (Leprosy patients of ethnic minorities in south China)disease, one of the most significant loci of the HLA-DQB1 gene was 6-32626438-A-T (p = 4.49E-08, OR = 0.36, 95%,CI: 0.25–0.52). Therefore, rs75324027 is a locus in M-S disease, and 6-32626438-a-T may be a new locus in M-SM disease. The interaction between 6 and 32626438-A-T and RS75324027 was analyzed, and A significant interaction relationship was found. In the optimal model, the accuracy of prediction was 0.5974, cross-validation Consistency:10, p = 0.0107. Conclusion: In conclusion, this study is the first to assess the association between HLA and leprosy susceptibility in Han and other minority populations in southern China using the Thousand Population database and the Han MHC database. In addition, our analysis validated the previously reported locus rs602875 in the HLA-DR region and for the first time identified an unreported independent locus in leprosy among ethnic minorities in southern China.
format Online
Article
Text
id pubmed-9234480
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-92344802022-06-28 Human Leukocyte Antigen Fine-Mapping and Correlation Analysis of Han and Minority Leprosy Patients in Southern China Li, Zhuo Wang, Yirui Fan, Wencheng Zhang, Chang Liu, Hao Zhang, Ruixue Cao, Lu Zhen, Qi Chen, Weiwei Yu, Yafen Li, Bao Mao, Yiwen Bai, Yuanming Wang, Daiyue Luo, Sihan Li, Yuanyuan Qin, Qin Ge, Huiyao Yong, Liang Hu, Xia Yu, Yanxia Sun, Liangdan Front Genet Genetics Backround: Leprosy is very prevalent in many populations around the world, which is well known that both alleles for human leukocyte antigen (HLA) as well as single nucleotide polymorphisms (SNPs) in the HLA region are common in leprosy patients. Previous studies have identified leprosy-associated susceptibility genes that explain only part of disease risk and heritability. In view of the complicated characteristics of the major histocompatibility complex (MHC) region, this study aimed to explore the development and variation of HLA in leprosy and its possible mechanism. Methods: Previous genome-wide association data were extracted from Han and minority populations in southern China for HLA fine-mapping studies. Insertion and deletion (INDEL), SNP, and copy number variation (CNV) imputation were determined by using the Thousand People Database (1KGP Phase 3 Dataset) as a reference panel. The HAN-MHC database was used to input the HLA classical alleles and amino acids in the MHC region, and further step-regression analysis was performed to analyze independent variation signals associated with leprosy. Results: The most significant locus rs75324027 (the same locus as rs602875 in the HLA-DR region) [p = 7.49E-09, OR= 0.62, 95%,CI: 0.52–0.73] in the intergene region between HLA-DQA1 and HLA-DRB1 was related with leprosy in M-S(Han leprosy patients in south China)disease. In M-SM (Leprosy patients of ethnic minorities in south China)disease, one of the most significant loci of the HLA-DQB1 gene was 6-32626438-A-T (p = 4.49E-08, OR = 0.36, 95%,CI: 0.25–0.52). Therefore, rs75324027 is a locus in M-S disease, and 6-32626438-a-T may be a new locus in M-SM disease. The interaction between 6 and 32626438-A-T and RS75324027 was analyzed, and A significant interaction relationship was found. In the optimal model, the accuracy of prediction was 0.5974, cross-validation Consistency:10, p = 0.0107. Conclusion: In conclusion, this study is the first to assess the association between HLA and leprosy susceptibility in Han and other minority populations in southern China using the Thousand Population database and the Han MHC database. In addition, our analysis validated the previously reported locus rs602875 in the HLA-DR region and for the first time identified an unreported independent locus in leprosy among ethnic minorities in southern China. Frontiers Media S.A. 2022-06-13 /pmc/articles/PMC9234480/ /pubmed/35769990 http://dx.doi.org/10.3389/fgene.2022.888361 Text en Copyright © 2022 Li, Wang, Fan, Zhang, Liu, Zhang, Cao, Zhen, Chen, Yu, Li, Mao, Bai, Wang, Luo, Li, Qin, Ge, Yong, Hu, Yu and Sun. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Li, Zhuo
Wang, Yirui
Fan, Wencheng
Zhang, Chang
Liu, Hao
Zhang, Ruixue
Cao, Lu
Zhen, Qi
Chen, Weiwei
Yu, Yafen
Li, Bao
Mao, Yiwen
Bai, Yuanming
Wang, Daiyue
Luo, Sihan
Li, Yuanyuan
Qin, Qin
Ge, Huiyao
Yong, Liang
Hu, Xia
Yu, Yanxia
Sun, Liangdan
Human Leukocyte Antigen Fine-Mapping and Correlation Analysis of Han and Minority Leprosy Patients in Southern China
title Human Leukocyte Antigen Fine-Mapping and Correlation Analysis of Han and Minority Leprosy Patients in Southern China
title_full Human Leukocyte Antigen Fine-Mapping and Correlation Analysis of Han and Minority Leprosy Patients in Southern China
title_fullStr Human Leukocyte Antigen Fine-Mapping and Correlation Analysis of Han and Minority Leprosy Patients in Southern China
title_full_unstemmed Human Leukocyte Antigen Fine-Mapping and Correlation Analysis of Han and Minority Leprosy Patients in Southern China
title_short Human Leukocyte Antigen Fine-Mapping and Correlation Analysis of Han and Minority Leprosy Patients in Southern China
title_sort human leukocyte antigen fine-mapping and correlation analysis of han and minority leprosy patients in southern china
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234480/
https://www.ncbi.nlm.nih.gov/pubmed/35769990
http://dx.doi.org/10.3389/fgene.2022.888361
work_keys_str_mv AT lizhuo humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT wangyirui humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT fanwencheng humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT zhangchang humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT liuhao humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT zhangruixue humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT caolu humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT zhenqi humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT chenweiwei humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT yuyafen humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT libao humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT maoyiwen humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT baiyuanming humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT wangdaiyue humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT luosihan humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT liyuanyuan humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT qinqin humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT gehuiyao humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT yongliang humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT huxia humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT yuyanxia humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina
AT sunliangdan humanleukocyteantigenfinemappingandcorrelationanalysisofhanandminorityleprosypatientsinsouthernchina