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Tumor necrosis factor-alpha G-238A polymorphism and coronary artery disease risk: a meta-analysis of 4,222 patients and 4,832 controls
BACKGROUND: The aim of the present study was to investigate the association between tumor necrosis factor-alpha (TNF-α) gene G-238A polymorphism and risk of coronary artery disease (CAD) using a meta-analytical approach. METHODS: The PubMed and Embase databases were searched for relevant publication...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4590639/ https://www.ncbi.nlm.nih.gov/pubmed/26445542 http://dx.doi.org/10.2147/TCRM.S87598 |
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author | Hua, Xian-Ping Zhang, Xiao-Dong Kwong, Joey SW Zeng, Xian-Tao Zhang, Zhen-Jian Wei, Wan-Lin |
author_facet | Hua, Xian-Ping Zhang, Xiao-Dong Kwong, Joey SW Zeng, Xian-Tao Zhang, Zhen-Jian Wei, Wan-Lin |
author_sort | Hua, Xian-Ping |
collection | PubMed |
description | BACKGROUND: The aim of the present study was to investigate the association between tumor necrosis factor-alpha (TNF-α) gene G-238A polymorphism and risk of coronary artery disease (CAD) using a meta-analytical approach. METHODS: The PubMed and Embase databases were searched for relevant publications up to January 13, 2015. Four authors (XPH, XDZ, XTZ, and ZJZ) independently selected the studies, extracted, and analyzed the data using the Comprehensive Meta-Analysis software. The sensitivity and subgroups analyses were also performed. Either a fixed effects or a random effects model was used to estimate pooled odds ratios (ORs) and their 95% confidence intervals (CIs). RESULTS: Finally, ten articles including eleven case-control studies involving 4,222 patients and 4,832 controls were yielded. The results indicated no significant association between G-238A polymorphism and CAD risk (A vs G: OR =1.08, 95% CI =0.89–1.30; AA vs GG: OR =1.15, 95% CI =0.59–2.25; GA vs GG: OR =1.14, 95% CI =0.88–1.48; AA vs [GG + GA]: OR =1.09, 95% CI =0.56–2.14; (GA + AA) vs GG: OR =1.11, 95% CI =0.90–1.38). In the subgroup analyses, similar results were obtained with overall populations. The sensitivity analyses showed that the overall results were robust. No publication bias was detected. CONCLUSION: Based on current evidence, we can conclude that TNF-α G-238A polymorphism might not be associated with CAD risk. |
format | Online Article Text |
id | pubmed-4590639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45906392015-10-06 Tumor necrosis factor-alpha G-238A polymorphism and coronary artery disease risk: a meta-analysis of 4,222 patients and 4,832 controls Hua, Xian-Ping Zhang, Xiao-Dong Kwong, Joey SW Zeng, Xian-Tao Zhang, Zhen-Jian Wei, Wan-Lin Ther Clin Risk Manag Original Research BACKGROUND: The aim of the present study was to investigate the association between tumor necrosis factor-alpha (TNF-α) gene G-238A polymorphism and risk of coronary artery disease (CAD) using a meta-analytical approach. METHODS: The PubMed and Embase databases were searched for relevant publications up to January 13, 2015. Four authors (XPH, XDZ, XTZ, and ZJZ) independently selected the studies, extracted, and analyzed the data using the Comprehensive Meta-Analysis software. The sensitivity and subgroups analyses were also performed. Either a fixed effects or a random effects model was used to estimate pooled odds ratios (ORs) and their 95% confidence intervals (CIs). RESULTS: Finally, ten articles including eleven case-control studies involving 4,222 patients and 4,832 controls were yielded. The results indicated no significant association between G-238A polymorphism and CAD risk (A vs G: OR =1.08, 95% CI =0.89–1.30; AA vs GG: OR =1.15, 95% CI =0.59–2.25; GA vs GG: OR =1.14, 95% CI =0.88–1.48; AA vs [GG + GA]: OR =1.09, 95% CI =0.56–2.14; (GA + AA) vs GG: OR =1.11, 95% CI =0.90–1.38). In the subgroup analyses, similar results were obtained with overall populations. The sensitivity analyses showed that the overall results were robust. No publication bias was detected. CONCLUSION: Based on current evidence, we can conclude that TNF-α G-238A polymorphism might not be associated with CAD risk. Dove Medical Press 2015-09-23 /pmc/articles/PMC4590639/ /pubmed/26445542 http://dx.doi.org/10.2147/TCRM.S87598 Text en © 2015 Hua et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Hua, Xian-Ping Zhang, Xiao-Dong Kwong, Joey SW Zeng, Xian-Tao Zhang, Zhen-Jian Wei, Wan-Lin Tumor necrosis factor-alpha G-238A polymorphism and coronary artery disease risk: a meta-analysis of 4,222 patients and 4,832 controls |
title | Tumor necrosis factor-alpha G-238A polymorphism and coronary artery disease risk: a meta-analysis of 4,222 patients and 4,832 controls |
title_full | Tumor necrosis factor-alpha G-238A polymorphism and coronary artery disease risk: a meta-analysis of 4,222 patients and 4,832 controls |
title_fullStr | Tumor necrosis factor-alpha G-238A polymorphism and coronary artery disease risk: a meta-analysis of 4,222 patients and 4,832 controls |
title_full_unstemmed | Tumor necrosis factor-alpha G-238A polymorphism and coronary artery disease risk: a meta-analysis of 4,222 patients and 4,832 controls |
title_short | Tumor necrosis factor-alpha G-238A polymorphism and coronary artery disease risk: a meta-analysis of 4,222 patients and 4,832 controls |
title_sort | tumor necrosis factor-alpha g-238a polymorphism and coronary artery disease risk: a meta-analysis of 4,222 patients and 4,832 controls |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4590639/ https://www.ncbi.nlm.nih.gov/pubmed/26445542 http://dx.doi.org/10.2147/TCRM.S87598 |
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