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dc.contributor.authorMagro-Checa, Cesares_ES
dc.contributor.authorRamiro, Sofiaes_ES
dc.contributor.authorRúa-Figueroa, Iñigoes_ES
dc.contributor.authorJimenez, Normanes_ES
dc.contributor.authorCampo-Pérez, Víctor deles_ES
dc.contributor.authorMartinez-Barrio, Juliaes_ES
dc.contributor.authorGalindo-Izquierdo, Maríaes_ES
dc.contributor.authorCalvo-Alén, Jaimees_ES
dc.contributor.authorUriarte-Itzazelaia, Estheres_ES
dc.contributor.authorTomero-Muriel, Evaes_ES
dc.contributor.authorFreire-González, Mercedeses_ES
dc.contributor.authorMartínez Taboada, Víctor Manuel es_ES
dc.contributor.authorSalgado, Evaes_ES
dc.contributor.authorVela, Palomaes_ES
dc.contributor.authorMena-Vázquez, Nataliaes_ES
dc.contributor.authorOlivé, Alejandroes_ES
dc.contributor.authorNarváez, Javieres_ES
dc.contributor.authorMenor-Almagro, Raúles_ES
dc.contributor.authorSantos-Soler, Gregorioes_ES
dc.contributor.authorHernández-Beriaín, José Aes_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2022-11-25T16:23:06Z
dc.date.available2022-11-25T16:23:06Z
dc.date.issued2023es_ES
dc.identifier.issn0049-0172es_ES
dc.identifier.issn1532-866Xes_ES
dc.identifier.urihttps://hdl.handle.net/10902/26625
dc.description.abstractObjectives To analyze the prevalence, incidence, survival and contribution on mortality of major central nervous system (CNS) involvement in systemic lupus erythematosus (SLE). Methods Patients fulfilling the SLE 1997 ACR classification criteria from the multicentre, retrospective RELESSER-TRANS (Spanish Society of Rheumatology Lupus Register) were included. Prevalence, incidence and survival rates of major CNS neuropsychiatric (NP)-SLE as a group and the individual NP manifestations cerebrovascular disease (CVD), seizure, psychosis, organic brain syndrome and transverse myelitis were calculated. Furthermore, the contribution of these manifestations on mortality was analysed in Cox regression models adjusted for confounders. Results A total of 3591 SLE patients were included. Of them, 412 (11.5%) developed a total of 522 major CNS NP-SLE manifestations. 61 patients (12%) with major CNS NP-SLE died. The annual mortality rate for patients with and without ever major CNS NP-SLE was 10.8% vs 3.8%, respectively. Individually, CVD (14%) and organic brain syndrome (15.5%) showed the highest mortality rates. The 10% mortality rate for patients with and without ever major CNS NP-SLE was reached after 12.3?vs 22.8 years, respectively. CVD (9.8 years) and organic brain syndrome (7.1 years) reached the 10% mortality rate earlier than other major CNS NP-SLE manifestations. Major CNS NP-SLE (HR 1.85, 1.29?2.67) and more specifically CVD (HR 2.17, 1.41?3.33) and organic brain syndrome (HR 2.11, 1.19?3.74) accounted as independent prognostic factors for poor survival. Conclusion The presentation of major CNS NP-SLE during the disease course contributes to a higher mortality, which may differ depending on the individual NP manifestation. CVD and organic brain syndrome are associated with the highest mortality rates.es_ES
dc.format.extent9 p.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights© 2023. This manuscript version is made available under the CC-BY-NC-ND 4.0 license*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceSeminars in Arthritis and Rheumatism Volume 58, February 2023, 152121es_ES
dc.subject.otherSystemic lupus erythematosuses_ES
dc.subject.otherNP-SLEes_ES
dc.subject.otherCentral nervous systemes_ES
dc.subject.otherSurvivales_ES
dc.subject.otherMortalityes_ES
dc.titleCentral nervous system involvement in systemic lupus erythematosus: Data from the Spanish Society of Rheumatology Lupus Register (RELESSER)es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1016/j.semarthrit.2022.152121es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1016/j.semarthrit.2022.152121es_ES
dc.type.versionacceptedVersiones_ES


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Attribution-NonCommercial-NoDerivatives 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution-NonCommercial-NoDerivatives 4.0 International