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dc.contributor.authorHerrero Morant, Alba
dc.contributor.authorFernández Ramón, Raúl
dc.contributor.authorPrieto Peña, Diana 
dc.contributor.authorMartín Varillas, José Luis
dc.contributor.authorCastañeda, Santos
dc.contributor.authorBlanco, Ricardo
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-10-16T07:17:15Z
dc.date.available2025-10-16T07:17:15Z
dc.date.issued2025
dc.identifier.issn2227-9059
dc.identifier.urihttps://hdl.handle.net/10902/37853
dc.description.abstractObjectives: Neurosarcoidosis (NS) is a severe and infrequent complication of sarcoidosis. Available data on NS are variable. We aimed to characterize NS epidemiology, clinical and therapeutic characteristics in a well-defined cohort of NS patients. Methods: Observational population-based cohort study of 342 patients diagnosed with sarcoidosis in Northern Spain, between 1999 and 2019. Among them, those patients who fulfilled the Consortium Consensus Group diagnosis criteria for NS were included. The annual incidence between 1999 and 2019 was estimated by gender, age, and year of diagnosis. Additionally, a literature review was performed. Therapeutic efficacy was evaluated using the neurological-related extra-pulmonary physician organ severity tool (ePOST). Results: NS was diagnosed in 29 out of 342 patients with sarcoidosis (8.5%; 18 women/11 men) with a mean age of 42.3 ± 15.1 years. Most NS patients have associated systemic sarcoidosis (93.4%) mainly consisting of lung (n = 22; 75.9%), articular (n = 15; 51.7%) and/or ocular (n = 12; 40%) involvement. The annual incidence of NS during the study period was 1.1 per 1,000,000 people. There is a linear relationship with a weak decrease in age at diagnosis over time. NS was subdivided into chronic headache (n = 11; 36.7%), cranial neuropathy (n = 7; 24.1%), myelitis (n = 4; 13.8%), peripheral neuropathy (n = 3; 10.3%), cranial neuropathy with chronic headache (n = 3; 10.3%) and aseptic meningitis (n = 2; 6.9%). Twenty-five patients (86.2%) received oral glucocorticoids (mean ± SD maximum prednisone dose 49.6 ± 19.4 mg/day). In addition, conventional immunosuppressive drugs were administered to 17 (58.6%) patients and biological therapy to 12 (41.4%) patients. After 12 months of initiating biological therapy, 14 out of 17 patients (82.4%) achieved complete remission, defined as an ePOST score of 0. Severe allergic reaction was observed in only one patient who had received treatment with both Infliximab and Adalimumab. Conclusions: The epidemiological, clinical and treatment characteristics of NS in Northern Spain are similar to that of other countrieses_ES
dc.format.extent12 p.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rights© 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.es_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceBiomedicines, 2025, 13(6), 1360es_ES
dc.subject.otherEpidemiologyes_ES
dc.subject.otherNeurosarcoidosises_ES
dc.subject.otherIncidencees_ES
dc.subject.otherClinical phenotypeses_ES
dc.subject.otherExtrapulmonary involvementes_ES
dc.subject.otherTreatmentes_ES
dc.subject.otherPrognosises_ES
dc.subject.otherBiological therapyes_ES
dc.subject.otherAutoinmunityes_ES
dc.subject.otherInflammationes_ES
dc.subject.otherSarcoidosises_ES
dc.titleEpidemiology, clinical features and treatment of neurosarcoidosis in northern Spaines_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.3390/biomedicines13061360es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.3390/biomedicines13061360
dc.type.versionpublishedVersiones_ES


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© 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.Excepto si se señala otra cosa, la licencia del ítem se describe como © 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.