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dc.contributor.authorCamacho-Encina, María
dc.contributor.authorBalboa-Barreiro, Vanesa
dc.contributor.authorRego-Perez, Ignacio
dc.contributor.authorPicchi, Florencia
dc.contributor.authorVanDuin, Jennifer
dc.contributor.authorQiu, Ji
dc.contributor.authorFuentes, Manuel
dc.contributor.authorOreiro, Natividad
dc.contributor.authorLaBaer, Joshua
dc.contributor.authorRuiz-Romero, Cristina
dc.contributor.authorBlanco, Francisco J.
dc.date.accessioned2025-01-17T17:32:12Z
dc.date.available2025-01-17T17:32:12Z
dc.date.issued2019
dc.identifier.citationCamacho-Encina, M., Balboa-Barreiro, V., Rego-Perez, I., Picchi, F., VanDuin, J., Qiu, J., ... & Blanco, F. J. (2019). Discovery of an autoantibody signature for the early diagnosis of knee osteoarthritis: data from the Osteoarthritis Initiative. Annals of the rheumatic diseases, 78(12), 1699-1705.es_ES
dc.identifier.issn0003-4967
dc.identifier.urihttp://hdl.handle.net/10366/161928
dc.descriptionArtículoes_ES
dc.description.abstract[EN]Objective To find autoantibodies (AAbs) in serum that could be useful to predict incidence of radiographic knee osteoarthritis (KOA). Design A Nucleic-acid Programmable Protein Arrays (NAPPA) platform was used to screen AAbs against 2125 human proteins in sera at baseline from participants free of radiographic KOA belonging to the incidence and non-exposed subcohorts of the Osteoarthritis Initiative (OAI) who developed or not, radiographic KOA during a follow-up period of 96 months. NAPPA-ELISA were performed to analyse reactivity against methionine adenosyltransferase two beta (MAT2β) and verify the results in 327 participants from the same subcohorts. The association of MAT2β-AAb levels with KOA incidence was assessed by combining several robust biostatistics analysis (logistic regression, Receiver Operating Characteristic and Kaplan-Meier curves). The proposed prognostic model was replicated in samples from the progression subcohort of the OAI. Results In the screening phase, six AAbs were found significantly different at baseline in samples from incident compared with non-incident participants. In the verification phase, high levels of MAT2β-AAb were significantly associated with the future incidence of KOA and with an earlier development of the disease. The incorporation of this AAb in a clinical model for the prognosis of incident radiographic KOA significantly improved the identification/classification of patients who will develop the disorder. The usefulness of the model to predict radiographic KOA was confirmed on a different OAI subcohort. Conclusions The measurement of AAbs against MAT2β in serum might be highly useful to improve the prediction of OA development, and also to estimate the time to incidence.es_ES
dc.description.sponsorshipInstituto de Salud Carlos IIIes_ES
dc.language.isoenges_ES
dc.publisherBMJ Publishing Groupes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectauto-inmunidades_ES
dc.subjectosteoartritises_ES
dc.subject.meshOsteoarthritis *
dc.subject.meshArthritis, Rheumatoid *
dc.titleDiscovery of an autoantibody signature for the early diagnosis of knee osteoarthritis: data from the Osteoarthritis Initiativees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1136/annrheumdis-2019-215325es_ES
dc.subject.unesco2412 Inmunologíaes_ES
dc.subject.unesco3205.09 Reumatologíaes_ES
dc.identifier.doi10.1136/ANNRHEUMDIS-2019-215325
dc.relation.projectIDDTS17/00200es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.journal.titleAnnals of the Rheumatic Diseaseses_ES
dc.volume.number78es_ES
dc.issue.number12es_ES
dc.page.initial1699es_ES
dc.page.final1705es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decsartritis reumatoide *
dc.subject.decsosteoartritis *
dc.description.projectInstituto de Salud Carlos IIIes_ES


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