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dc.contributor.authorLlorca Díaz, Francisco Javier es_ES
dc.contributor.authorFerraz Amaro, Ivánes_ES
dc.contributor.authorCastañeda, Santoses_ES
dc.contributor.authorPlaza, Zulemaes_ES
dc.contributor.authorSánchez-Alonso, Fernandoes_ES
dc.contributor.authorGarcía Gómez, Carmenes_ES
dc.contributor.authorGonzález Juanatey, Carloses_ES
dc.contributor.authorGonzález-Gay Mantecón, Miguel Ángel es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-12-23T11:54:03Z
dc.date.available2025-12-23T11:54:03Z
dc.date.issued2025es_ES
dc.identifier.issn0049-0172es_ES
dc.identifier.issn1532-866Xes_ES
dc.identifier.urihttps://hdl.handle.net/10902/38636
dc.description.abstractObjective: To identify significant predictors of cardiovascular (CV) events in rheumatoid arthritis (RA) patients from the CARdiovascular in RheuMAtology (CARMA) project, followed prospectively for 10 years. Methods: Between July 2010 and January 2012, 708 RA patients were recruited from 67 hospitals across Spain. The study focused on patients with no prior CV events at the time of recruitment. At the 10-year follow-up, data on the occurrence of CV events, patient-years of follow-up and linearized event rates were analyzed. Cox regression analyses were conducted, both crude and adjusted for PREVENT-CVD. Results: Over 6608 patient-years, 114 patients (16.1%) experienced CV events, yielding a linearized event rate of 1.73 per 100 patient-years. Patients with CV events were older (70.7± 10.6 vs. 62.1±12.8 years, p<0.001), more frequently male (36.0% vs. 20.0%, p<0.001), and had higher rates of hypertension (46.5% vs. 23.4%, p<0.001), diabetes (14% vs. 4.9%, p=0.001), and dyslipidemia (37.7% vs. 27.4%, p=0.03). Higher baseline erythrocyte sedimentation rate (ESR) was also associated with future CV events. Those who developed CV events had a significantly higher predicted 10-year CV risk using the PREVENT-CVD score (18.0% vs. 10.3%, p<0.001). Cox regression analysis adjusted for PREVENT-CVD showed that although higher crude C-reactive protein and uric acid levels were associated with increased CV risk, after adjustment these associations weakened and became non-significant. However, higher disease activity (DAS28-ESR) was linked to greater CV risk, with moderate/high disease activity (DAS28-ESR>3.2) showing a significantly higher adjusted CV risk (HR 1.62; 95% CI: 1.06-22.47, p=0.03). Conclusions: Disease activity is a key determinant of CV outcomes in RA patients. The PREVENT-CVD score is an effective tool for CV risk stratification in this population.es_ES
dc.description.sponsorshipProf. Gonzalez-Gay's research is supported by the Spanish Ministry of Health, Instituto de Salud Carlos III (ISCIII), PI24/00554, and cofunded by the European Union. Additionally, he is funded by the Spanish Research Network RICORS - RD24/0007/0031, through Next Generation EU funds, which support the initiatives of the Recovery and Resilience Mechanism (MRR). Dr. Ferraz-Amaro research is supported by the Spanish Ministry of Health, Instituto de Salud Carlos III (ISCIII), co-funded by the European Union (PI23/00046).es_ES
dc.format.extent7 p.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rights© 2025 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY license*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceSeminars in Arthritis and Rheumatism, 75, 152833es_ES
dc.subject.otherRheumatoid arthritises_ES
dc.subject.otherCardiovascular riskes_ES
dc.subject.otherDAS28-ESR
dc.subject.otherDisease activityes_ES
dc.subject.otherPREVENTes_ES
dc.titleDisease activity predicts the development of cardiovascular events in patients with rheumatoid arthritis from the CARMA cohortes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1016/j.semarthrit.2025.152833es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1016/j.semarthrit.2025.152833es_ES
dc.type.versionpublishedVersiones_ES


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© 2025 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY licenseExcepto si se señala otra cosa, la licencia del ítem se describe como © 2025 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY license