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The associations between interleukin 10 polymorphisms and susceptibility to autoimmune uveitis – a meta-analysis
Autoimmune uveitis is an ocular inflammatory disease that is associated with genetic factors. Interleukin 10 (IL-10) is an immune-regulatory cytokine of autoimmune diseases. IL-10 is considered a candidate gene for uveitis. We evaluate the association of IL-10 with susceptibility to autoimmune uveit...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Polish Society of Experimental and Clinical Immunology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953374/ https://www.ncbi.nlm.nih.gov/pubmed/31933534 http://dx.doi.org/10.5114/ceji.2019.89596 |
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author | Jung, Jae Hyun Song, Gwan Gyu Kim, Jae-Hoon Choi, Sung Jae |
author_facet | Jung, Jae Hyun Song, Gwan Gyu Kim, Jae-Hoon Choi, Sung Jae |
author_sort | Jung, Jae Hyun |
collection | PubMed |
description | Autoimmune uveitis is an ocular inflammatory disease that is associated with genetic factors. Interleukin 10 (IL-10) is an immune-regulatory cytokine of autoimmune diseases. IL-10 is considered a candidate gene for uveitis. We evaluate the association of IL-10 with susceptibility to autoimmune uveitis. The results from seven studies were pooled in the meta-analysis, covering a total of 2893 cases of uveitis and 4873 controls. Published literature from MEDLINE and Embase was retrieved. Meta-analyses were conducted on the associations between autoimmune uveitis and the -1082 A/G and -819 C/T polymorphisms of the IL-10 gene. The meta-analysis revealed no association between uveitis and the IL-10 -1082 A allele (OR = 0.91, 95% CI = 0.64-1.30, p = 0.62). The recessive, dominant, and homozygous models of the IL-10 -1082 A/G allele also suggested no association between autoimmune uveitis and each genotype. The meta-analysis revealed significant association between uveitis and the -892 C allele (OR = 0.81, 95% CI = 0.67-0.98, p = 0.03). In addition, significant association was found in homozygous models (OR = 0.58, 95% CI = 0.36-0.92, p = 0.02). However, the dominant and recessive models of the IL-10 -819 C/T polymorphisms showed no association between uveitis and each genotype. This meta-analysis showed that the -1082 A/G polymorphisms of IL-10 were not associated with autoimmune uveitis, but the -819 C/T polymorphisms were significantly associated with uveitis. |
format | Online Article Text |
id | pubmed-6953374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Polish Society of Experimental and Clinical Immunology |
record_format | MEDLINE/PubMed |
spelling | pubmed-69533742020-01-13 The associations between interleukin 10 polymorphisms and susceptibility to autoimmune uveitis – a meta-analysis Jung, Jae Hyun Song, Gwan Gyu Kim, Jae-Hoon Choi, Sung Jae Cent Eur J Immunol Experimental Immunology Autoimmune uveitis is an ocular inflammatory disease that is associated with genetic factors. Interleukin 10 (IL-10) is an immune-regulatory cytokine of autoimmune diseases. IL-10 is considered a candidate gene for uveitis. We evaluate the association of IL-10 with susceptibility to autoimmune uveitis. The results from seven studies were pooled in the meta-analysis, covering a total of 2893 cases of uveitis and 4873 controls. Published literature from MEDLINE and Embase was retrieved. Meta-analyses were conducted on the associations between autoimmune uveitis and the -1082 A/G and -819 C/T polymorphisms of the IL-10 gene. The meta-analysis revealed no association between uveitis and the IL-10 -1082 A allele (OR = 0.91, 95% CI = 0.64-1.30, p = 0.62). The recessive, dominant, and homozygous models of the IL-10 -1082 A/G allele also suggested no association between autoimmune uveitis and each genotype. The meta-analysis revealed significant association between uveitis and the -892 C allele (OR = 0.81, 95% CI = 0.67-0.98, p = 0.03). In addition, significant association was found in homozygous models (OR = 0.58, 95% CI = 0.36-0.92, p = 0.02). However, the dominant and recessive models of the IL-10 -819 C/T polymorphisms showed no association between uveitis and each genotype. This meta-analysis showed that the -1082 A/G polymorphisms of IL-10 were not associated with autoimmune uveitis, but the -819 C/T polymorphisms were significantly associated with uveitis. Polish Society of Experimental and Clinical Immunology 2019-09-30 2019 /pmc/articles/PMC6953374/ /pubmed/31933534 http://dx.doi.org/10.5114/ceji.2019.89596 Text en Copyright: © 2019 Polish Society of Experimental and Clinical Immunology http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Experimental Immunology Jung, Jae Hyun Song, Gwan Gyu Kim, Jae-Hoon Choi, Sung Jae The associations between interleukin 10 polymorphisms and susceptibility to autoimmune uveitis – a meta-analysis |
title | The associations between interleukin 10 polymorphisms and susceptibility to autoimmune uveitis – a meta-analysis |
title_full | The associations between interleukin 10 polymorphisms and susceptibility to autoimmune uveitis – a meta-analysis |
title_fullStr | The associations between interleukin 10 polymorphisms and susceptibility to autoimmune uveitis – a meta-analysis |
title_full_unstemmed | The associations between interleukin 10 polymorphisms and susceptibility to autoimmune uveitis – a meta-analysis |
title_short | The associations between interleukin 10 polymorphisms and susceptibility to autoimmune uveitis – a meta-analysis |
title_sort | associations between interleukin 10 polymorphisms and susceptibility to autoimmune uveitis – a meta-analysis |
topic | Experimental Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953374/ https://www.ncbi.nlm.nih.gov/pubmed/31933534 http://dx.doi.org/10.5114/ceji.2019.89596 |
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