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The effect of CTLA-4 A49G polymorphism on rheumatoid arthritis risk: a meta-analysis

BACKGROUND: Recently, a number of studies have been performed to explore the association between CTLA-4 A49G polymorphism and rheumatoid arthritis (RA). However, the results of previous works are still controversial and ambiguous. METHODS: In this work, we attempted to perform an updated meta-analys...

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Detalles Bibliográficos
Autores principales: Li, Gang, Shi, Fengjun, Liu, Jingchen, Li, Ye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4160544/
https://www.ncbi.nlm.nih.gov/pubmed/25128482
http://dx.doi.org/10.1186/s13000-014-0157-0
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author Li, Gang
Shi, Fengjun
Liu, Jingchen
Li, Ye
author_facet Li, Gang
Shi, Fengjun
Liu, Jingchen
Li, Ye
author_sort Li, Gang
collection PubMed
description BACKGROUND: Recently, a number of studies have been performed to explore the association between CTLA-4 A49G polymorphism and rheumatoid arthritis (RA). However, the results of previous works are still controversial and ambiguous. METHODS: In this work, we attempted to perform an updated meta-analysis of available case–control study in order to assess the association between CTLA-4 A49G polymorphism and RA risk. We searched the various citation databases without limits on languages. Article searching was performed by screening the references of retrieved studies manually. Odds ratios (OR) and 95% confidence intervals (95% CI) were calculated to evaluate the strength of the association. RESULTS: We totally compiled 27 studies in 24 articles (9805 RA patients and 10691 control subjects) into our meta-analysis work. We found significant association between CTL-A4 A49G polymorphism and RA risk (GG vs. AA: OR = 1.13, 95% CI = 1.03–1.23; GA vs. AA: OR = 1.19, 95% CI = 1.07–1.33; GA + GG vs. AA: OR = 1.18, 95% CI = 1.07–1.29). In the subgroup analysis by ethnicity, evidences of significantly increased risk was also found in both Asian (GG vs. AA: OR = 1.34, 95% CI = 1.15–1.55; GA + GG vs. AA: OR = 1.24, 95% CI = 1.08–1.41) and Caucasian population (GA vs. AA: OR = 1.19, 95% CI = 1.03–1.37; GA + GG vs. AA: OR = 1.14, 95% CI = 1.01–1.29). No evidence of publication bias was found in this work. CONCLUSIONS: Our meta-analysis suggests that CTLA-4 A49G polymorphism was associated with RA risk. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/13000_2014_157
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spelling pubmed-41605442014-09-12 The effect of CTLA-4 A49G polymorphism on rheumatoid arthritis risk: a meta-analysis Li, Gang Shi, Fengjun Liu, Jingchen Li, Ye Diagn Pathol Research BACKGROUND: Recently, a number of studies have been performed to explore the association between CTLA-4 A49G polymorphism and rheumatoid arthritis (RA). However, the results of previous works are still controversial and ambiguous. METHODS: In this work, we attempted to perform an updated meta-analysis of available case–control study in order to assess the association between CTLA-4 A49G polymorphism and RA risk. We searched the various citation databases without limits on languages. Article searching was performed by screening the references of retrieved studies manually. Odds ratios (OR) and 95% confidence intervals (95% CI) were calculated to evaluate the strength of the association. RESULTS: We totally compiled 27 studies in 24 articles (9805 RA patients and 10691 control subjects) into our meta-analysis work. We found significant association between CTL-A4 A49G polymorphism and RA risk (GG vs. AA: OR = 1.13, 95% CI = 1.03–1.23; GA vs. AA: OR = 1.19, 95% CI = 1.07–1.33; GA + GG vs. AA: OR = 1.18, 95% CI = 1.07–1.29). In the subgroup analysis by ethnicity, evidences of significantly increased risk was also found in both Asian (GG vs. AA: OR = 1.34, 95% CI = 1.15–1.55; GA + GG vs. AA: OR = 1.24, 95% CI = 1.08–1.41) and Caucasian population (GA vs. AA: OR = 1.19, 95% CI = 1.03–1.37; GA + GG vs. AA: OR = 1.14, 95% CI = 1.01–1.29). No evidence of publication bias was found in this work. CONCLUSIONS: Our meta-analysis suggests that CTLA-4 A49G polymorphism was associated with RA risk. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/13000_2014_157 BioMed Central 2014-08-16 /pmc/articles/PMC4160544/ /pubmed/25128482 http://dx.doi.org/10.1186/s13000-014-0157-0 Text en © Li et al.; licensee BioMed Central Ltd. 2014 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
Li, Gang
Shi, Fengjun
Liu, Jingchen
Li, Ye
The effect of CTLA-4 A49G polymorphism on rheumatoid arthritis risk: a meta-analysis
title The effect of CTLA-4 A49G polymorphism on rheumatoid arthritis risk: a meta-analysis
title_full The effect of CTLA-4 A49G polymorphism on rheumatoid arthritis risk: a meta-analysis
title_fullStr The effect of CTLA-4 A49G polymorphism on rheumatoid arthritis risk: a meta-analysis
title_full_unstemmed The effect of CTLA-4 A49G polymorphism on rheumatoid arthritis risk: a meta-analysis
title_short The effect of CTLA-4 A49G polymorphism on rheumatoid arthritis risk: a meta-analysis
title_sort effect of ctla-4 a49g polymorphism on rheumatoid arthritis risk: a meta-analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4160544/
https://www.ncbi.nlm.nih.gov/pubmed/25128482
http://dx.doi.org/10.1186/s13000-014-0157-0
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