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

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dc.contributor.authorLee, Young Ho-
dc.contributor.authorBae, Sang-Cheol-
dc.contributor.authorChoi, Sung Jae-
dc.contributor.authorJi, Jong Dae-
dc.contributor.authorSong, Gwan Gyu-
dc.date.accessioned2021-08-02T19:29:04Z-
dc.date.available2021-08-02T19:29:04Z-
dc.date.created2021-05-12-
dc.date.issued2012-05-
dc.identifier.issn0301-4851-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/27537-
dc.description.abstractThe 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.-
dc.language영어-
dc.language.isoen-
dc.publisherSPRINGER-
dc.titleAssociation between the CTLA-4+49 A/G polymorphism and susceptibility to rheumatoid arthritis: a meta-analysis-
dc.typeArticle-
dc.contributor.affiliatedAuthorBae, Sang-Cheol-
dc.identifier.doi10.1007/s11033-011-1364-3-
dc.identifier.scopusid2-s2.0-84863750045-
dc.identifier.wosid000302147800062-
dc.identifier.bibliographicCitationMOLECULAR BIOLOGY REPORTS, v.39, no.5, pp.5599 - 5605-
dc.relation.isPartOfMOLECULAR BIOLOGY REPORTS-
dc.citation.titleMOLECULAR BIOLOGY REPORTS-
dc.citation.volume39-
dc.citation.number5-
dc.citation.startPage5599-
dc.citation.endPage5605-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.subject.keywordPlusSYSTEMIC-LUPUS-ERYTHEMATOSUS-
dc.subject.keywordPlusGENE POLYMORPHISM-
dc.subject.keywordPlusCTLA4 POLYMORPHISMS-
dc.subject.keywordPlusEXON-1 POLYMORPHISM-
dc.subject.keywordPlusJAPANESE PATIENTS-
dc.subject.keywordPlusPOPULATION-
dc.subject.keywordPlusCHINESE-
dc.subject.keywordPlusPROMOTER-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusREGIONS-
dc.subject.keywordAuthorRheumatoid arthritis-
dc.subject.keywordAuthorCTLA-4-
dc.subject.keywordAuthorPolymorphism-
dc.subject.keywordAuthorMeta-analysis-
dc.identifier.urlhttps://link.springer.com/article/10.1007%2Fs11033-011-1364-3-
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