Cargando…
HLA-DRB1 polymorphisms and alopecia areata disease risk: A systematic review and meta-analysis
BACKGROUND: Published studies have reported conflicting and heterogeneous results regarding the association between human leukocyte antigen (HLA)-DRB1 polymorphisms and alopecia areata (AA). This study aimed to review and quantitatively analyze the association between HLA-DRB1 polymorphisms and AA....
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133534/ https://www.ncbi.nlm.nih.gov/pubmed/30095639 http://dx.doi.org/10.1097/MD.0000000000011790 |
_version_ | 1783354534305726464 |
---|---|
author | Ji, Conghua Liu, Shan Zhu, Kan Luo, Hongbin Li, Qiushuang Zhang, Ying Huang, Sijia Chen, Qing Cao, Yi |
author_facet | Ji, Conghua Liu, Shan Zhu, Kan Luo, Hongbin Li, Qiushuang Zhang, Ying Huang, Sijia Chen, Qing Cao, Yi |
author_sort | Ji, Conghua |
collection | PubMed |
description | BACKGROUND: Published studies have reported conflicting and heterogeneous results regarding the association between human leukocyte antigen (HLA)-DRB1 polymorphisms and alopecia areata (AA). This study aimed to review and quantitatively analyze the association between HLA-DRB1 polymorphisms and AA. METHODS: In this study, all relevant publications were searched through December 2016. Odds ratios (ORs) and confidence intervals (CIs) for comparisons between case and control groups were calculated. Stata 14.0 software was used to perform statistical analysis. This research does not require formal ethical approval because the data used in this analysis do not involve personal information and thus do not affect privacy. RESULTS: Twelve articles were identified. For HLA-DRB1∗04 and HLA-DRB1∗16 polymorphisms, the OR (95% CIs) was 1.49 (1.24–1.78) and 1.61 (1.08–2.41), and P was <.01 and <.01, respectively. For HLA-DRB1∗0301, HLA-DRB1∗09, and HLA-DRB1∗13 polymorphisms, the OR (95% CIs) was 0.42 (0.28–0.63), 0.74 (0.55–0.99), and 0.62 (0.40–0.98), and P was <.01, <.01, and <.01, respectively. Statistical evidence revealed no publication bias (P > .05). CONCLUSION: The present meta-analysis suggested that HLA-DRB1∗04 and HLA-DRB1∗16 polymorphisms might be associated with increased AA risk, while HLA-DRB1∗0301, HLA-DRB1∗09, and HLA-DRB1∗13 polymorphisms might decrease the AA risk. Studies with adequate methodological quality on gene–gene and gene–environment interactions are needed to validate the results in the future. |
format | Online Article Text |
id | pubmed-6133534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-61335342018-09-19 HLA-DRB1 polymorphisms and alopecia areata disease risk: A systematic review and meta-analysis Ji, Conghua Liu, Shan Zhu, Kan Luo, Hongbin Li, Qiushuang Zhang, Ying Huang, Sijia Chen, Qing Cao, Yi Medicine (Baltimore) Research Article BACKGROUND: Published studies have reported conflicting and heterogeneous results regarding the association between human leukocyte antigen (HLA)-DRB1 polymorphisms and alopecia areata (AA). This study aimed to review and quantitatively analyze the association between HLA-DRB1 polymorphisms and AA. METHODS: In this study, all relevant publications were searched through December 2016. Odds ratios (ORs) and confidence intervals (CIs) for comparisons between case and control groups were calculated. Stata 14.0 software was used to perform statistical analysis. This research does not require formal ethical approval because the data used in this analysis do not involve personal information and thus do not affect privacy. RESULTS: Twelve articles were identified. For HLA-DRB1∗04 and HLA-DRB1∗16 polymorphisms, the OR (95% CIs) was 1.49 (1.24–1.78) and 1.61 (1.08–2.41), and P was <.01 and <.01, respectively. For HLA-DRB1∗0301, HLA-DRB1∗09, and HLA-DRB1∗13 polymorphisms, the OR (95% CIs) was 0.42 (0.28–0.63), 0.74 (0.55–0.99), and 0.62 (0.40–0.98), and P was <.01, <.01, and <.01, respectively. Statistical evidence revealed no publication bias (P > .05). CONCLUSION: The present meta-analysis suggested that HLA-DRB1∗04 and HLA-DRB1∗16 polymorphisms might be associated with increased AA risk, while HLA-DRB1∗0301, HLA-DRB1∗09, and HLA-DRB1∗13 polymorphisms might decrease the AA risk. Studies with adequate methodological quality on gene–gene and gene–environment interactions are needed to validate the results in the future. Wolters Kluwer Health 2018-08-10 /pmc/articles/PMC6133534/ /pubmed/30095639 http://dx.doi.org/10.1097/MD.0000000000011790 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-sa/4.0 This is an open access article distributed under the Creative Commons Attribution-ShareAlike License 4.0, which allows others to remix, tweak, and build upon the work, even for commercial purposes, as long as the author is credited and the new creations are licensed under the identical terms. http://creativecommons.org/licenses/by-sa/4.0 |
spellingShingle | Research Article Ji, Conghua Liu, Shan Zhu, Kan Luo, Hongbin Li, Qiushuang Zhang, Ying Huang, Sijia Chen, Qing Cao, Yi HLA-DRB1 polymorphisms and alopecia areata disease risk: A systematic review and meta-analysis |
title | HLA-DRB1 polymorphisms and alopecia areata disease risk: A systematic review and meta-analysis |
title_full | HLA-DRB1 polymorphisms and alopecia areata disease risk: A systematic review and meta-analysis |
title_fullStr | HLA-DRB1 polymorphisms and alopecia areata disease risk: A systematic review and meta-analysis |
title_full_unstemmed | HLA-DRB1 polymorphisms and alopecia areata disease risk: A systematic review and meta-analysis |
title_short | HLA-DRB1 polymorphisms and alopecia areata disease risk: A systematic review and meta-analysis |
title_sort | hla-drb1 polymorphisms and alopecia areata disease risk: a systematic review and meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133534/ https://www.ncbi.nlm.nih.gov/pubmed/30095639 http://dx.doi.org/10.1097/MD.0000000000011790 |
work_keys_str_mv | AT jiconghua hladrb1polymorphismsandalopeciaareatadiseaseriskasystematicreviewandmetaanalysis AT liushan hladrb1polymorphismsandalopeciaareatadiseaseriskasystematicreviewandmetaanalysis AT zhukan hladrb1polymorphismsandalopeciaareatadiseaseriskasystematicreviewandmetaanalysis AT luohongbin hladrb1polymorphismsandalopeciaareatadiseaseriskasystematicreviewandmetaanalysis AT liqiushuang hladrb1polymorphismsandalopeciaareatadiseaseriskasystematicreviewandmetaanalysis AT zhangying hladrb1polymorphismsandalopeciaareatadiseaseriskasystematicreviewandmetaanalysis AT huangsijia hladrb1polymorphismsandalopeciaareatadiseaseriskasystematicreviewandmetaanalysis AT chenqing hladrb1polymorphismsandalopeciaareatadiseaseriskasystematicreviewandmetaanalysis AT caoyi hladrb1polymorphismsandalopeciaareatadiseaseriskasystematicreviewandmetaanalysis |