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dc.contributor.authorMartín-González, Candelariaes_ES
dc.contributor.authorFerrer-Moure, Carmenes_ES
dc.contributor.authorQuevedo-Abeledo, Juan Carloses_ES
dc.contributor.authorVera-González, Antonia dees_ES
dc.contributor.authorGonzález-Delgado, Alejandraes_ES
dc.contributor.authorSánchez-Martín, Julioes_ES
dc.contributor.authorGonzález-Gay Mantecón, Miguel Ángel es_ES
dc.contributor.authorFerraz-Amaro, Ivánes_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2023-03-28T07:57:36Z
dc.date.available2023-03-28T07:57:36Z
dc.date.issued2022es_ES
dc.identifier.issn1478-6354es_ES
dc.identifier.issn1478-6362es_ES
dc.identifier.urihttps://hdl.handle.net/10902/28393
dc.description.abstractBackground: Systemic lupus erythematosus (SLE) has been associated with atherosclerotic cardiovascular disease (CV) and an altered lipid profile. High levels of apolipoprotein C-III (ApoC3) are associated with elevated triglyceride levels and an increased risk of CV. In the present study, we aimed to study circulating ApoC3 in patients with SLE and describe its relationship with the manifestations of the disease. Methods: This is a cross-sectional study that included 186 patients with SLE. Disease-related data, CV comorbidity, full lipid profile, and serum levels of ApoC3 were assessed. A multivariable regression analysis was performed to study how ApoC3 was related to SLE features. Results: Classic CV risk factors were significantly and strongly associated with circulating ApoC3. After a fully multivariable analysis that included classic CV risk factors and lipid profile molecules, SLICC damage (beta coef. 0.10 [95% CI 0.02?0.19] mg/dl, 0.020) and Katz severity (beta coef. 0.11 [95% CI 0.03-0.19] mg/dl, p = 0.011) indices and SLEDAI activity score (beta coef. 0.05 [95% CI 0.05-0.08] mg/dl, p = 0.004) were all independently associated with higher levels of circulating ApoC3. Conclusion: Among SLE patients, disease activity, severity, and disease damage are independently associated with higher ApoC3 serum levels.es_ES
dc.description.sponsorshipFunding: This work was supported by a grant to I.F-A. from the Spanish Ministry of Health, Subdirección General de Evaluación y Fomento de la Investigación, Plan Estatal de Investigación Científica y Técnica y de Innovación 2013–2016 and by Fondo Europeo de Desarrollo Regional—FEDER—(Fondo de Investigaciones Sanitarias, PI17/00083).es_ES
dc.format.extent8 p.es_ES
dc.language.isoenges_ES
dc.publisherBioMed Centrales_ES
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceArthritis Research & Therapy, 2022, 24(104)es_ES
dc.subject.otherSystemic lupus erythematosuses_ES
dc.subject.otherApolipoprotein C3es_ES
dc.titleApolipoprotein C-III in patients with systemic lupus erythematosuses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1186/s13075-022-02793-yes_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1186/s13075-022-02793-yes_ES
dc.type.versionpublishedVersiones_ES


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