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IL-10 Polymorphisms and Tuberculosis Susceptibility: An Updated Meta-Analysis

PURPOSE: The association of interleukin-10 (IL-10) polymorphisms (-1082G/A, -819C/T, -592A/C) and interleukin-6 (IL-6) poly-morphisms (-174G/C) with tuberculosis (TB) risk has been widely reported. However, the results are controversial. To clarify the role of these polymorphisms in TB, we performed...

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Autores principales: Ke, Zunqiong, Yuan, Leyong, Ma, Jun, Zhang, Xiaoyan, Guo, Yi, Xiong, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4541657/
https://www.ncbi.nlm.nih.gov/pubmed/26256970
http://dx.doi.org/10.3349/ymj.2015.56.5.1274
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author Ke, Zunqiong
Yuan, Leyong
Ma, Jun
Zhang, Xiaoyan
Guo, Yi
Xiong, Hui
author_facet Ke, Zunqiong
Yuan, Leyong
Ma, Jun
Zhang, Xiaoyan
Guo, Yi
Xiong, Hui
author_sort Ke, Zunqiong
collection PubMed
description PURPOSE: The association of interleukin-10 (IL-10) polymorphisms (-1082G/A, -819C/T, -592A/C) and interleukin-6 (IL-6) poly-morphisms (-174G/C) with tuberculosis (TB) risk has been widely reported. However, the results are controversial. To clarify the role of these polymorphisms in TB, we performed a meta-analysis of all available and relevant published studies. MATERIALS AND METHODS: Based on comprehensive searches of the PubMed, Medline, Embase, Web of Science, Elsevier Science Direct and Cochrane Library database, we identified outcome data from all articles estimating the association between IL-10 and IL-6 polymorphisms and TB risk. RESULTS: The results indicated significant association of the allele model, heterozygous model and dominant model of IL-6 -174G/C polymorphism with decreased risk of TB. In the stratified analysis by ethnicity, significantly increased risk was observed for IL-10 -1082G/A polymorphism in Europeans under recessive model, for IL-10 -819C/T polymorphism in Asians under heterozygous model and dominant model and IL-10 -592A/C polymorphism in Asians under Allele model, homozygous model and recessive model. Moreover, significantly decreased risk of TB was associated with Asians for IL-6 -174C/G polymorphism in allele model, heterozygous model and dominant model. We also performed the analyses by sample types in IL-10 -1082G/A polymorphism, and observed significantly increased TB risk in mixed group under homozygous model. CONCLUSION: The results suggested that the IL-10 -1082G/A polymorphism is associated with increased TB risk in Europeans, while IL-10 -819C/T and IL-10 -592A/C polymorphisms in Asians. However, IL-6 -174G/C polymorphism might be a genetic risk factor that decreases TB susceptibility in Asians.
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spelling pubmed-45416572015-09-01 IL-10 Polymorphisms and Tuberculosis Susceptibility: An Updated Meta-Analysis Ke, Zunqiong Yuan, Leyong Ma, Jun Zhang, Xiaoyan Guo, Yi Xiong, Hui Yonsei Med J Original Article PURPOSE: The association of interleukin-10 (IL-10) polymorphisms (-1082G/A, -819C/T, -592A/C) and interleukin-6 (IL-6) poly-morphisms (-174G/C) with tuberculosis (TB) risk has been widely reported. However, the results are controversial. To clarify the role of these polymorphisms in TB, we performed a meta-analysis of all available and relevant published studies. MATERIALS AND METHODS: Based on comprehensive searches of the PubMed, Medline, Embase, Web of Science, Elsevier Science Direct and Cochrane Library database, we identified outcome data from all articles estimating the association between IL-10 and IL-6 polymorphisms and TB risk. RESULTS: The results indicated significant association of the allele model, heterozygous model and dominant model of IL-6 -174G/C polymorphism with decreased risk of TB. In the stratified analysis by ethnicity, significantly increased risk was observed for IL-10 -1082G/A polymorphism in Europeans under recessive model, for IL-10 -819C/T polymorphism in Asians under heterozygous model and dominant model and IL-10 -592A/C polymorphism in Asians under Allele model, homozygous model and recessive model. Moreover, significantly decreased risk of TB was associated with Asians for IL-6 -174C/G polymorphism in allele model, heterozygous model and dominant model. We also performed the analyses by sample types in IL-10 -1082G/A polymorphism, and observed significantly increased TB risk in mixed group under homozygous model. CONCLUSION: The results suggested that the IL-10 -1082G/A polymorphism is associated with increased TB risk in Europeans, while IL-10 -819C/T and IL-10 -592A/C polymorphisms in Asians. However, IL-6 -174G/C polymorphism might be a genetic risk factor that decreases TB susceptibility in Asians. Yonsei University College of Medicine 2015-09-01 2015-07-29 /pmc/articles/PMC4541657/ /pubmed/26256970 http://dx.doi.org/10.3349/ymj.2015.56.5.1274 Text en © Copyright: Yonsei University College of Medicine 2015 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ke, Zunqiong
Yuan, Leyong
Ma, Jun
Zhang, Xiaoyan
Guo, Yi
Xiong, Hui
IL-10 Polymorphisms and Tuberculosis Susceptibility: An Updated Meta-Analysis
title IL-10 Polymorphisms and Tuberculosis Susceptibility: An Updated Meta-Analysis
title_full IL-10 Polymorphisms and Tuberculosis Susceptibility: An Updated Meta-Analysis
title_fullStr IL-10 Polymorphisms and Tuberculosis Susceptibility: An Updated Meta-Analysis
title_full_unstemmed IL-10 Polymorphisms and Tuberculosis Susceptibility: An Updated Meta-Analysis
title_short IL-10 Polymorphisms and Tuberculosis Susceptibility: An Updated Meta-Analysis
title_sort il-10 polymorphisms and tuberculosis susceptibility: an updated meta-analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4541657/
https://www.ncbi.nlm.nih.gov/pubmed/26256970
http://dx.doi.org/10.3349/ymj.2015.56.5.1274
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