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IL-23R mutation is associated with ulcerative colitis: A systemic review and meta-analysis
OBJECTIVES: Since a genome-wide association study revealed that Interleukin-23 receptor (IL-23R) gene is a candidate gene for Ulcerative Colitis (UC), many studies have investigated the association between the IL-23R polymorphisms and UC. However, the results were controversial. The aim of the study...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354875/ https://www.ncbi.nlm.nih.gov/pubmed/27902482 http://dx.doi.org/10.18632/oncotarget.13607 |
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author | Peng, Ling-Long Wang, Ying Zhu, Feng-Ling Xu, Wang-Dong Ji, Xue-Lei Ni, Jing |
author_facet | Peng, Ling-Long Wang, Ying Zhu, Feng-Ling Xu, Wang-Dong Ji, Xue-Lei Ni, Jing |
author_sort | Peng, Ling-Long |
collection | PubMed |
description | OBJECTIVES: Since a genome-wide association study revealed that Interleukin-23 receptor (IL-23R) gene is a candidate gene for Ulcerative Colitis (UC), many studies have investigated the association between the IL-23R polymorphisms and UC. However, the results were controversial. The aim of the study was to determine whether the IL-23R polymorphisms confer susceptibility to UC. METHODS: A systematic literature search was carried out to identify all potentially relevant studies. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were used to estimate the strength of association. RESULTS: A total of 33 studies in 32 articles, including 10,527 UC cases and 15,142 healthy controls, were finally involved in the meta-analysis. Overall, a significant association was found between all UC cases and the rs11209026A allele (OR = 0.665, 95% CI = 0.604~0.733, P < 0.001). Similarly, meta-analyses of the rs7517847, rs1004819, rs10889677, rs2201841, rs11209032, rs1495965, rs1343151 and rs11465804 polymorphisms also indicated significant association with all UC (all P < 0.05). Stratification by ethnicity revealed that the rs11209026, rs7517847, rs10889677, rs2201841 andrs11465804 polymorphisms were associated with UC in the Caucasian group, but not in Asians, while the rs1004819 and rs11209032 polymorphisms were found to be related to UC for both Caucasian and Asian groups. However, subgroup analysis failed to unveil any association between the rs1495965 and rs1343151 polymorphisms and UC in Caucasians or Asians. CONCLUSIONS: The meta-analysis suggests significant association between IL-23R polymorphisms and UC, especially in Caucasians. |
format | Online Article Text |
id | pubmed-5354875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53548752017-04-24 IL-23R mutation is associated with ulcerative colitis: A systemic review and meta-analysis Peng, Ling-Long Wang, Ying Zhu, Feng-Ling Xu, Wang-Dong Ji, Xue-Lei Ni, Jing Oncotarget Research Paper OBJECTIVES: Since a genome-wide association study revealed that Interleukin-23 receptor (IL-23R) gene is a candidate gene for Ulcerative Colitis (UC), many studies have investigated the association between the IL-23R polymorphisms and UC. However, the results were controversial. The aim of the study was to determine whether the IL-23R polymorphisms confer susceptibility to UC. METHODS: A systematic literature search was carried out to identify all potentially relevant studies. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were used to estimate the strength of association. RESULTS: A total of 33 studies in 32 articles, including 10,527 UC cases and 15,142 healthy controls, were finally involved in the meta-analysis. Overall, a significant association was found between all UC cases and the rs11209026A allele (OR = 0.665, 95% CI = 0.604~0.733, P < 0.001). Similarly, meta-analyses of the rs7517847, rs1004819, rs10889677, rs2201841, rs11209032, rs1495965, rs1343151 and rs11465804 polymorphisms also indicated significant association with all UC (all P < 0.05). Stratification by ethnicity revealed that the rs11209026, rs7517847, rs10889677, rs2201841 andrs11465804 polymorphisms were associated with UC in the Caucasian group, but not in Asians, while the rs1004819 and rs11209032 polymorphisms were found to be related to UC for both Caucasian and Asian groups. However, subgroup analysis failed to unveil any association between the rs1495965 and rs1343151 polymorphisms and UC in Caucasians or Asians. CONCLUSIONS: The meta-analysis suggests significant association between IL-23R polymorphisms and UC, especially in Caucasians. Impact Journals LLC 2016-11-25 /pmc/articles/PMC5354875/ /pubmed/27902482 http://dx.doi.org/10.18632/oncotarget.13607 Text en Copyright: © 2017 Peng et al. http://creativecommons.org/licenses/by/3.0/ 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 credited. |
spellingShingle | Research Paper Peng, Ling-Long Wang, Ying Zhu, Feng-Ling Xu, Wang-Dong Ji, Xue-Lei Ni, Jing IL-23R mutation is associated with ulcerative colitis: A systemic review and meta-analysis |
title | IL-23R mutation is associated with ulcerative colitis: A systemic review and meta-analysis |
title_full | IL-23R mutation is associated with ulcerative colitis: A systemic review and meta-analysis |
title_fullStr | IL-23R mutation is associated with ulcerative colitis: A systemic review and meta-analysis |
title_full_unstemmed | IL-23R mutation is associated with ulcerative colitis: A systemic review and meta-analysis |
title_short | IL-23R mutation is associated with ulcerative colitis: A systemic review and meta-analysis |
title_sort | il-23r mutation is associated with ulcerative colitis: a systemic review and meta-analysis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354875/ https://www.ncbi.nlm.nih.gov/pubmed/27902482 http://dx.doi.org/10.18632/oncotarget.13607 |
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