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Meta-analysis of tumor necrosis factor alpha -308 polymorphism and knee osteoarthritis risk
BACKGROUND: Several case–control studies have been conducted to clarify the association between the tumor necrosis factor alpha (TNF-α) -G308A polymorphism and risk of osteoarthritis (OA); however, the results are inconsistent. This meta-analysis was performed to clarify this issue using all the ava...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289255/ https://www.ncbi.nlm.nih.gov/pubmed/25398219 http://dx.doi.org/10.1186/1471-2474-15-373 |
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author | Kou, Suotang Wu, Yaochi |
author_facet | Kou, Suotang Wu, Yaochi |
author_sort | Kou, Suotang |
collection | PubMed |
description | BACKGROUND: Several case–control studies have been conducted to clarify the association between the tumor necrosis factor alpha (TNF-α) -G308A polymorphism and risk of osteoarthritis (OA); however, the results are inconsistent. This meta-analysis was performed to clarify this issue using all the available evidence. METHODS: Eligible articles were retrieved by searching PubMed, Web of science and Google scholar. The strength of the association between the TNF-α -G308A polymorphism and risk of OA was assessed by odds ratios (ORs) with the corresponding 95% confidence interval (CI) for each study. RESULTS: Seven studies were included in the meta-analysis, which included 983 OA cases and 1355 controls. The pooled analysis based on all included studies showed a significantly increased OA risk in the recessive genetic model analysis (OR = 11.08, 95% CI = 4.75-25.86, p < 0.001) and in the A allele vs. G allele analysis (OR = 2.30, 95% CI = 1.08-4.90). However, there was no statistical difference in the dominant genetic model analysis (OR = 2.45, 95% CI = 0.95-6.27, p = 0.06). Furthermore, we found that OA patients had a higher frequency of the AA genotype (OR = 10.49, 95% CI = 4.47-24.61) and GA genotype (OR = 1.78, 95% CI = 1.03-3.08) compared with the control population. CONCLUSION: Our results suggested that the TNF-α -G308A polymorphism were associated with an increased risk of OA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2474-15-373) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4289255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42892552015-01-11 Meta-analysis of tumor necrosis factor alpha -308 polymorphism and knee osteoarthritis risk Kou, Suotang Wu, Yaochi BMC Musculoskelet Disord Research Article BACKGROUND: Several case–control studies have been conducted to clarify the association between the tumor necrosis factor alpha (TNF-α) -G308A polymorphism and risk of osteoarthritis (OA); however, the results are inconsistent. This meta-analysis was performed to clarify this issue using all the available evidence. METHODS: Eligible articles were retrieved by searching PubMed, Web of science and Google scholar. The strength of the association between the TNF-α -G308A polymorphism and risk of OA was assessed by odds ratios (ORs) with the corresponding 95% confidence interval (CI) for each study. RESULTS: Seven studies were included in the meta-analysis, which included 983 OA cases and 1355 controls. The pooled analysis based on all included studies showed a significantly increased OA risk in the recessive genetic model analysis (OR = 11.08, 95% CI = 4.75-25.86, p < 0.001) and in the A allele vs. G allele analysis (OR = 2.30, 95% CI = 1.08-4.90). However, there was no statistical difference in the dominant genetic model analysis (OR = 2.45, 95% CI = 0.95-6.27, p = 0.06). Furthermore, we found that OA patients had a higher frequency of the AA genotype (OR = 10.49, 95% CI = 4.47-24.61) and GA genotype (OR = 1.78, 95% CI = 1.03-3.08) compared with the control population. CONCLUSION: Our results suggested that the TNF-α -G308A polymorphism were associated with an increased risk of OA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2474-15-373) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-15 /pmc/articles/PMC4289255/ /pubmed/25398219 http://dx.doi.org/10.1186/1471-2474-15-373 Text en © Kou and Wu; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Kou, Suotang Wu, Yaochi Meta-analysis of tumor necrosis factor alpha -308 polymorphism and knee osteoarthritis risk |
title | Meta-analysis of tumor necrosis factor alpha -308 polymorphism and knee osteoarthritis risk |
title_full | Meta-analysis of tumor necrosis factor alpha -308 polymorphism and knee osteoarthritis risk |
title_fullStr | Meta-analysis of tumor necrosis factor alpha -308 polymorphism and knee osteoarthritis risk |
title_full_unstemmed | Meta-analysis of tumor necrosis factor alpha -308 polymorphism and knee osteoarthritis risk |
title_short | Meta-analysis of tumor necrosis factor alpha -308 polymorphism and knee osteoarthritis risk |
title_sort | meta-analysis of tumor necrosis factor alpha -308 polymorphism and knee osteoarthritis risk |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289255/ https://www.ncbi.nlm.nih.gov/pubmed/25398219 http://dx.doi.org/10.1186/1471-2474-15-373 |
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