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Cited 4 time in webofscience Cited 4 time in scopus
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Associations between TRAF1-C5 Gene Polymorphisms and Rheumatoid Arthritis: A Meta-Analysis

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dc.contributor.authorSong, Gwan Gyu-
dc.contributor.authorBae, Sang-Cheol-
dc.contributor.authorKim, Jae-Hoon-
dc.contributor.authorLee, Young Ho-
dc.date.accessioned2021-08-02T18:28:58Z-
dc.date.available2021-08-02T18:28:58Z-
dc.date.issued2014-10-
dc.identifier.issn0882-0139-
dc.identifier.issn1532-4311-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/25754-
dc.description.abstractObjective: The aim of this study is to determine whether tumor necrosis factor receptor-associated factor 1-complement 5 (TRAF1-C5) polymorphisms are associated with susceptibility to rheumatoid arthritis (RA) in different populations. Methods: We conducted a meta-analysis of associations between the TRAF1-C5 polymorphisms and RA susceptibility. Results: A total of 24 comparative studies were included in this meta-analysis, including 22,682 patients with RA and 23,493 controls. The meta-analysis showed an association between the second allele of rs10818488 and RA in Europeans, but not in Asians (OR 1.229, 95% CI 1.094-1.381, p = 0.001; OR 1.060, 95% CI 0.930-1.335, p = 0.092). The meta-analysis also indicated an association between the second allele of rs3761847 and RA in Europeans, but not in Asians (OR 1.156, 95% CI 1.006-1.327, p = 0.041; OR 1.049, 95% CI 0.952-1.156, p = 0.333). The meta-analysis revealed an association between the second allele of the rs2900180 and rs10760130 polymorphisms and RA risk in Europeans (OR 1.224, 95% CI 1.065-1.405, p = 0.004; OR 1.072, 95% CI 1.002-1.147, p = 0.042). Conclusions: This meta-analysis confirms that the TRAF1-C5 rs10818488, rs3761847, rs2900180 and rs10760130 polymorphisms are associated with RA susceptibility in Europeans.-
dc.format.extent16-
dc.language영어-
dc.language.isoENG-
dc.publisherMarcel Dekker Inc.-
dc.titleAssociations between TRAF1-C5 Gene Polymorphisms and Rheumatoid Arthritis: A Meta-Analysis-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.3109/08820139.2013.837917-
dc.identifier.scopusid2-s2.0-84893423258-
dc.identifier.wosid000330710100001-
dc.identifier.bibliographicCitationImmunological Investigations, v.43, no.2, pp 97 - 112-
dc.citation.titleImmunological Investigations-
dc.citation.volume43-
dc.citation.number2-
dc.citation.startPage97-
dc.citation.endPage112-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordPlusSYSTEMIC-LUPUS-ERYTHEMATOSUS-
dc.subject.keywordPlusGENOME SCAN METAANALYSIS-
dc.subject.keywordPlusHAN CHINESE POPULATION-
dc.subject.keywordPlusSUSCEPTIBILITY LOCI-
dc.subject.keywordPlusSIGNALING PATHWAY-
dc.subject.keywordPlusWIDE ASSOCIATION-
dc.subject.keywordPlusTRAF1/C5-
dc.subject.keywordPlusRISK-
dc.subject.keywordPlusVARIANTS-
dc.subject.keywordPlusSTAT4-
dc.subject.keywordAuthorMeta-analysis-
dc.subject.keywordAuthorrheumatoid arthritis-
dc.subject.keywordAuthorpolymorphism-
dc.subject.keywordAuthorTRAF1-C5-
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