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Association between the functional ITGAM rs1143679 G/A polymorphism and systemic lupus erythematosus/lupus nephritis or rheumatoid arthritis: an update meta-analysis

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dc.contributor.authorLee, Young Ho-
dc.contributor.authorBae, Sang-Cheol-
dc.date.accessioned2021-08-02T17:56:13Z-
dc.date.available2021-08-02T17:56:13Z-
dc.date.issued2015-05-
dc.identifier.issn0172-8172-
dc.identifier.issn1437-160X-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/24972-
dc.description.abstractThe aim of this study was to determine whether the functional integrin-alpha-M (ITGAM) rs1143679 polymorphism is associated with susceptibility to systemic lupus erythematosus (SLE), lupus nephritis (LN), and rheumatoid arthritis (RA). A series of meta-analyses were conducted to test for associations between the ITGAM rs1143679 polymorphism and SLE, LN, or RA. A total of 24 comparisons involving 7,738 patients and 8,309 controls for SLE, and 2,663 patients and 2,694 controls in RA were considered. Meta-analysis showed a significant association between the ITGAM rs1143679 A allele and SLE in all subjects (OR 1.773, 95 % CI 1.656, 1.901, p < 1.0 x 10(-9)). After stratification by ethnicity, the A allele was found to be significantly associated with SLE in European, Latin American, and Asian. A significant association was also found between the ITGAM A allele and lupus nephritis in Europeans (OR 2.131, 95 % CI 1.565, 2.903, p = 1.6 x 10(-7)). However, no association was found between RA and the ITGAM rs1143679 polymorphism. Our meta-analyses confirm that the ITGAM rs1143679 polymorphism is associated with SLE susceptibility in different ethnic groups and demonstrate that the polymorphism is associated with LN in European.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherSpringer Verlag-
dc.titleAssociation between the functional ITGAM rs1143679 G/A polymorphism and systemic lupus erythematosus/lupus nephritis or rheumatoid arthritis: an update meta-analysis-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.1007/s00296-014-3156-2-
dc.identifier.scopusid2-s2.0-84928801648-
dc.identifier.wosid000353354800004-
dc.identifier.bibliographicCitationRheumatology International, v.35, no.5, pp 815 - 823-
dc.citation.titleRheumatology International-
dc.citation.volume35-
dc.citation.number5-
dc.citation.startPage815-
dc.citation.endPage823-
dc.type.docTypeReview-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaRheumatology-
dc.relation.journalWebOfScienceCategoryRheumatology-
dc.subject.keywordPlusGENETIC SUSCEPTIBILITY LOCI-
dc.subject.keywordPlusGENOME SCAN METAANALYSIS-
dc.subject.keywordPlusDISEASE SUSCEPTIBILITY-
dc.subject.keywordPlusVARIANT-
dc.subject.keywordPlusCD11B-
dc.subject.keywordPlusR77H-
dc.subject.keywordPlusREPLICATION-
dc.subject.keywordPlusPOPULATION-
dc.subject.keywordPlusSLE-
dc.subject.keywordAuthorSystemic lupus erythematosus-
dc.subject.keywordAuthorRheumatoid arthritis-
dc.subject.keywordAuthorITGAM-
dc.subject.keywordAuthorPolymorphism-
dc.subject.keywordAuthorMeta-analysis-
dc.identifier.urlhttps://link.springer.com/article/10.1007%2Fs00296-014-3156-2-
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