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dc.creatorLopez-Rodriguez R., Perez-Pampin E., Marquez A., Blanco F.J., Joven B., Carreira P., Ferrer M.A., Caliz R., Valor L., Narvaez J., Cañete J.D., Del Carmen Ordoñez M., Manrique-Arija S., Vasilopoulos Y., Balsa A., Pascual-Salcedo D., Moreno-Ramos M.J., Alegre-Sancho J.J., Navarro-Sarabia F., Moreira V., Garcia-Portales R., Raya E., Magro-Checa C., Martin J., Gomez-Reino J.J., Gonzalez A.en
dc.date.accessioned2023-01-31T08:55:25Z
dc.date.available2023-01-31T08:55:25Z
dc.date.issued2018
dc.identifier10.1371/journal.pone.0196793
dc.identifier.issn19326203
dc.identifier.urihttp://hdl.handle.net/11615/76000
dc.description.abstractGenetic biomarkers are sought to personalize treatment of patients with rheumatoid arthritis (RA), given their variable response to TNF inhibitors (TNFi). However, no genetic biomaker is yet sufficiently validated. Here, we report a validation study of 18 previously reported genetic biomarkers, including 11 from GWAS of response to TNFi. The validation was attempted in 581 patients with RA that had not been treated with biologic antirheumatic drugs previously. Their response to TNFi was evaluated at 3, 6 and 12 months in two ways: change in the DAS28 measure of disease activity, and according to the EULAR criteria for response to antirheumatic drugs. Association of these parameters with the genotypes, obtained by PCR amplification followed by single-base extension, was tested with regression analysis. These analyses were adjusted for baseline DAS28, sex, and the specific TNFi. However, none of the proposed biomarkers was validated, as none showed association with response to TNFi in our study, even at the time of assessment and with the outcome that showed the most significant result in previous studies. These negative results are notable because this was the first independent validation study for 12 of the biomarkers, and because they indicate that prudence is needed in the interpretation of the proposed biomarkers of response to TNFi even when they are supported by very low p values. The results also emphasize the requirement of independent replication for validation, and the need to search protocols that could increase reproducibility of the biomarkers of response to TNFi. © 2018 Lopez-Rodriguez et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en
dc.language.isoenen
dc.sourcePLoS ONEen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85046634415&doi=10.1371%2fjournal.pone.0196793&partnerID=40&md5=a5b8f92fd8d3264d603f0b2e8d744527
dc.subjectadalimumaben
dc.subjectbiological markeren
dc.subjectetanercepten
dc.subjectinfliximaben
dc.subjecttumor necrosis factor inhibitoren
dc.subjectantirheumatic agenten
dc.subjectTNF protein, humanen
dc.subjecttumor necrosis factoren
dc.subjectadulten
dc.subjectArticleen
dc.subjectcontrolled studyen
dc.subjectDAS28en
dc.subjectdisease activityen
dc.subjectdrug responseen
dc.subjectfemaleen
dc.subjectgene amplificationen
dc.subjectgenetic associationen
dc.subjectgenome-wide association studyen
dc.subjecthumanen
dc.subjectmajor clinical studyen
dc.subjectmaleen
dc.subjectmiddle ageden
dc.subjectoutcome assessmenten
dc.subjectpolymerase chain reactionen
dc.subjectreproducibilityen
dc.subjectrheumatoid arthritisen
dc.subjectsingle nucleotide polymorphismen
dc.subjecttreatment durationen
dc.subjectantagonists and inhibitorsen
dc.subjectgenetic markeren
dc.subjectgeneticsen
dc.subjectgenotypeen
dc.subjectrheumatoid arthritisen
dc.subjectAntirheumatic Agentsen
dc.subjectArthritis, Rheumatoiden
dc.subjectFemaleen
dc.subjectGenetic Markersen
dc.subjectGenotypeen
dc.subjectHumansen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectReproducibility of Resultsen
dc.subjectTumor Necrosis Factor-alphaen
dc.subjectPublic Library of Scienceen
dc.titleValidation study of genetic biomarkers of response to TNF inhibitors in rheumatoid arthritisen
dc.typejournalArticleen


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