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The miR-146a polymorphism and susceptibility to systemic lupus erythematosus and rheumatoid arthritis A meta-analysis

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dc.contributor.authorLee, Y. H.-
dc.contributor.authorBae, S. -C.-
dc.date.accessioned2021-08-02T18:26:22Z-
dc.date.available2021-08-02T18:26:22Z-
dc.date.created2021-05-12-
dc.date.issued2015-03-
dc.identifier.issn0340-1855-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/25622-
dc.description.abstractObjective The aim of this study was to explore whether the miR-146a polymorphism (rs2910164) confers susceptibility to systemic lupus erythematous (SLE) and rheumatoid arthritis (RA). Methods A meta-analysis was conducted on the association of the miR-146a polymorphism with SLE and RA. Results Five studies with 2013 patients and 2555 controls were included in the meta-analysis. Meta-analysis revealed no association between SLE and the miR-146a G allele (odds ratio, OR = 1.007, 95 % confidence interval, CI = 0.910–1.114, p = 0.888). Additionally, no associations were found between the miR-146a polymorphism and SLE using recessive or dominant models, or homozygote contrast. Meta-analysis using allele contrast, recessive and dominant models, as well as homozygote contrast failed to reveal an association between the miR-146a polymorphism and RA (OR for G allele = 1.114, 95 % CI = 0.892–1.391, p = 0.342). Conclusion This meta-analysis demonstrates that the miR-146a polymorphism is not associated with susceptibility to SLE and RA. However, considering the small number of studies, further studies are needed to confirm this result.-
dc.language영어-
dc.language.isoen-
dc.publisherSPRINGER HEIDELBERG-
dc.titleThe miR-146a polymorphism and susceptibility to systemic lupus erythematosus and rheumatoid arthritis A meta-analysis-
dc.typeArticle-
dc.contributor.affiliatedAuthorBae, S. -C.-
dc.identifier.doi10.1007/s00393-014-1509-6-
dc.identifier.scopusid2-s2.0-84939962499-
dc.identifier.wosid000351708900017-
dc.identifier.bibliographicCitationZEITSCHRIFT FUR RHEUMATOLOGIE, v.74, no.2, pp.153 - 156-
dc.relation.isPartOfZEITSCHRIFT FUR RHEUMATOLOGIE-
dc.citation.titleZEITSCHRIFT FUR RHEUMATOLOGIE-
dc.citation.volume74-
dc.citation.number2-
dc.citation.startPage153-
dc.citation.endPage156-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaRheumatology-
dc.relation.journalWebOfScienceCategoryRheumatology-
dc.subject.keywordPlusGENOME SCAN METAANALYSIS-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusCARCINOMA-
dc.subject.keywordAuthorMicroRNAs-
dc.subject.keywordAuthorAutoimmune disease-
dc.subject.keywordAuthorInflammatory disease-
dc.subject.keywordAuthorEthnicity-
dc.subject.keywordAuthorPolymorphism, single nucleotide-
dc.identifier.urlhttps://link.springer.com/article/10.1007%2Fs00393-014-1509-6-
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