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Association between the CTLA-4+49 A/G polymorphism and susceptibility to rheumatoid arthritis: a meta-analysis

Authors
Lee, Young HoBae, Sang-CheolChoi, Sung JaeJi, Jong DaeSong, Gwan Gyu
Issue Date
5월-2012
Publisher
SPRINGER
Keywords
Rheumatoid arthritis; CTLA-4; Polymorphism; Meta-analysis
Citation
MOLECULAR BIOLOGY REPORTS, v.39, no.5, pp.5599 - 5605
Indexed
SCIE
SCOPUS
Journal Title
MOLECULAR BIOLOGY REPORTS
Volume
39
Number
5
Start Page
5599
End Page
5605
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/108614
DOI
10.1007/s11033-011-1364-3
ISSN
0301-4851
Abstract
The aim of this study was to explore whether the cytotoxic T lymphocyte antigen-4 (CTLA-4) +49 A/G polymorphism confers susceptibility to rheumatoid arthritis (RA). A meta-analysis was conducted on the associations between CTLA-4 +49 A/G polymorphism and RA using; 1) allele contrast, 2) the recessive model, 3) the dominant model, and 4) an additive model. A total of 19 studies, 5,752 RA patients and 5,508 controls, encompassing 9 Caucasian, 8 Asian, 1 Mexican, and 1 Tunisian population were included in this meta-analysis. Ethnicity-specific meta-analysis was performed on Caucasian and Asian populations. Meta-analysis of the CTLA-4 +49 A/G polymorphism revealed an association between RA and the CTLA-4 +49 G allele in all 11,260 study subjects (odds ratio (OR) 1.118, 95% confidence interval (CI) 1.033-1.210, P = 0.005). Stratification by ethnicity showed an association between the CTLA-4 +49 G allele and RA in Asians (OR 1.164, 95% CI 1.056-1.283, P = 0.002), but no evidence of an association in Caucasians (OR 1.085, 95% CI 0.973-1.209, P = 0.431). Furthermore, associations were found between RA and the CTLA-4 +49 A/G polymorphism in Asians using the dominant and additive models, but not using the recessive model. On the other hand, no association was found between RA and the CTLA-4 +49 A/G polymorphism using the recessive, dominant, or additive models in Caucasians. This meta-analysis demonstrates that the CTLA-4 +49 A/G polymorphism confers susceptibility to RA in Asians, but not in Caucasians.
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