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Gene expression profile predicting the response to anti-TNF treatment in patients with rheumatoid arthritis; analysis of GEO datasets

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dc.contributor.authorKim, Tae-Hwan-
dc.contributor.authorChoi, Sung Jae-
dc.contributor.authorLee, Young Ho-
dc.contributor.authorSong, Gwan Gyu-
dc.contributor.authorJi, Jong Bae-
dc.date.accessioned2022-07-16T03:56:26Z-
dc.date.available2022-07-16T03:56:26Z-
dc.date.created2021-05-12-
dc.date.issued2014-07-
dc.identifier.issn1297-319X-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/159581-
dc.description.abstractObjectives: Anti-tumor necrosis factor (TNF) therapy is the treatment of choice for rheumatoid arthritis (RA) patients in whom standard disease-modifying anti-rheumatic drugs are ineffective. However, a substantial proportion of RA patients treated with anti-TNF agents do not show a significant clinical response. Therefore, biomarkers predicting response to anti-TNF agents are needed. Recently, gene expression profiling has been applied in research for developing such biomarkers. Methods: We compared gene expression profiles reported by previous studies dealing with the responsiveness of anti-TNF therapy in RA patients and attempted to identify differentially expressed genes (DEGs) that discriminated between responders and non-responders to anti-TNF therapy. We used microarray datasets available at the National Center for Biotechnology Information (NCBI) Gene Expression Omnibus (GEO). Results: This analysis included 6 studies and 5 sets of microarray data that used peripheral blood samples for identification of DEGs predicting response to anti-TNF therapy. We found little overlap in the DEGs that were highly ranked in each study. Three DEGs including IL2RB, SH2D2A and G0S2 appeared in more than 1 study. In addition, a meta-analysis designed to increase statistical power found one DEG, G0S2 by the Fisher's method. Conclusion: Our finding suggests the possibility that G0S2 plays as a biomarker to predict response to anti-TNF therapy in patients with rheumatoid arthritis. Further investigations based on larger studies are therefore needed to confirm the significance of G0S2 in predicting response to anti-TNF therapy.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER-
dc.titleGene expression profile predicting the response to anti-TNF treatment in patients with rheumatoid arthritis; analysis of GEO datasets-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Tae-Hwan-
dc.identifier.doi10.1016/j.jbspin.2014.01.013-
dc.identifier.scopusid2-s2.0-84904135761-
dc.identifier.wosid000339706500009-
dc.identifier.bibliographicCitationJOINT BONE SPINE, v.81, no.4, pp.325 - 330-
dc.relation.isPartOfJOINT BONE SPINE-
dc.citation.titleJOINT BONE SPINE-
dc.citation.volume81-
dc.citation.number4-
dc.citation.startPage325-
dc.citation.endPage330-
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.keywordPlusWHITE BLOOD-CELLS-
dc.subject.keywordPlusMICROARRAY METAANALYSIS-
dc.subject.keywordPlusGENOMIC METAANALYSIS-
dc.subject.keywordPlusQUALITY-CONTROL-
dc.subject.keywordPlusINFLIXIMAB-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusADALIMUMAB-
dc.subject.keywordPlusSIGNATURE-
dc.subject.keywordAuthorRheumatoid arthritis-
dc.subject.keywordAuthorAnti-TNF-
dc.subject.keywordAuthorResponse-
dc.subject.keywordAuthorMicroarray-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S1297319X14000347?via%3Dihub-
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