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dc.contributor.authorMontes Martínez, Ariadna
dc.contributor.authorPérez Pampín, Eva 
dc.contributor.authorJoven, B
dc.contributor.authorCarreira, P
dc.contributor.authorFernández-Nebro, A
dc.contributor.authorDel Carmen Ordoñez, M
dc.contributor.authorNavarro Sarabia, F
dc.contributor.authorMoreira, V
dc.contributor.authorVasilopoulos, Y
dc.contributor.authorSarafidou, T
dc.contributor.authorCaliz, R
dc.contributor.authorFerrer, MA
dc.contributor.authorCañete, JD
dc.contributor.authorde la Serna, AR
dc.contributor.authorMagallares, B
dc.contributor.authorNarváez, J
dc.contributor.authorGómez-Reino Carnota, Juan Jesús 
dc.contributor.authorGonzalez, A
dc.date.accessioned2023-06-16T06:51:43Z
dc.date.available2023-06-16T06:51:43Z
dc.date.issued2015-04
dc.identifier.issn1462-2416
dc.identifier.urihttp://hdl.handle.net/20.500.11940/17662
dc.description.abstract[EN] Objectives: Reproducible association of a functional polymorphism in FCGR2A with response to a TNF inhibitor (TNFi) in patients with rheumatoid arthritis (RA) led us to explore other FcγR functional polymorphisms. Methods: Functional polymorphisms FCGR3A F158V, FCGR2B I223T and promoter VNTR in FCGRT were analyzed in up to 429 patients with RA. Response to TNFi was recorded during standard care at 3, 6 and 12 months of follow-up. Fixed effects meta-analysis of studies addressing FCGR3A F158V polymorphism, which is the most studied of these polymorphisms, was conducted with inverse variance weighting. Results: None of the functional polymorphisms were associated with change in DAS28. Meta-analysis of the seven studies (899 patients) with available data addressing association of FCGR3A F158V with response to TNFi in RA showed no association (OR: 1.11, 95% CI: 0.8-1.5; p = 0.5). Conclusion: None of the three functional polymorphisms in FcγR genes showed association with response to TNFi in patients with RA. These negative results were obtained in spite of the larger size of this study relative to previous studies addressing the same polymorphisms. In addition, meta-analysis of FCGR3A F158V was also negative against the results provided by previous studies.es
dc.language.isoenges
dc.subject.meshBiomarkers, Pharmacological*
dc.subject.meshArthritis, Rheumatoid*
dc.subject.meshReceptors, Fc*
dc.subject.meshRheumatology*
dc.subject.meshInfliximab*
dc.subject.meshEtanercept*
dc.subject.meshSpain*
dc.subject.meshArthritis*
dc.subject.meshGenotype*
dc.subject.meshAdalimumab*
dc.titleFCGR polymorphisms in the treatment of rheumatoid arthritis with Fc-containing TNF inhibitorses
dc.typeArtigoes
dc.rights.holderFuture Medicine Ltdes
dc.bbddEmbase*
dc.bbddWOK*
dc.identifier.doi10.2217/pgs.14.175
dc.identifier.pmid25823782
dc.issue.number4es
dc.journal.titlePharmacogenomicses
dc.journal.titlePHARMACOGENOMICS [ISSN:1462-2416]*
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.)::Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS)es
dc.page.initial333es
dc.page.final345es
dc.relation.publisherversionhttps://www.futuremedicine.com/doi/10.2217/pgs.14.175?url_ver=Z39.88-2003&rfr_id=ori%3Arid%3Acrossref.org&rfr_dat=cr_pub++0pubmedes
dc.rights.accessRightsopenAccesses
dc.subject.decsbiomarcadores farmacológicos*
dc.subject.decsreceptores Fc*
dc.subject.decsgenotipo*
dc.subject.decsreumatología*
dc.subject.decsartritis reumatoide*
dc.subject.decsartritis*
dc.subject.keywordFCGRTes
dc.subject.keywordTNF inhibitorses
dc.subject.keywordCHUSes
dc.subject.keywordIDISes
dc.typefidesArtigo Científico (inclue Orixinal, Orixinal breve, Revisión Sistemática e Meta-análisis)es
dc.typesophosArtículo Originales
dc.volume.number16es


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