Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/54935
Campo DC Valoridioma
dc.contributor.authorTorrente-Segarra, V.en_US
dc.contributor.authorSalman Monte, T. C.en_US
dc.contributor.authorRúa Figueroa, I.en_US
dc.contributor.authorDe Uña-Álvarez, J.en_US
dc.contributor.authorBalboa-Barreiro, V.en_US
dc.contributor.authorLópez-Longo, F. J.en_US
dc.contributor.authorGalindo-Izquierdo, M.en_US
dc.contributor.authorCalvo-Alén, J.en_US
dc.contributor.authorOlivé-Marqués, A.en_US
dc.contributor.authorMouriño-Rodríguez, C.en_US
dc.contributor.authorHorcada, L.en_US
dc.contributor.authorSánchez-Atrio, A.en_US
dc.contributor.authorMontilla, C.en_US
dc.contributor.authorSalgado, E.en_US
dc.contributor.authorDíez-Álvarez, E.en_US
dc.contributor.authorBlanco, R.en_US
dc.contributor.authorAndreu, J. L.en_US
dc.contributor.authorFernández-Berrizbeitia, O.en_US
dc.contributor.authorHernández-Beriain, J. A.en_US
dc.contributor.authorGantes, M.en_US
dc.contributor.authorHernández-Cruz, B.en_US
dc.contributor.authorPecondón-Español, A.en_US
dc.contributor.authorMarras, C.en_US
dc.contributor.authorBonilla, G.en_US
dc.contributor.authorPego-Reigosa, J. M.en_US
dc.date.accessioned2019-02-18T15:46:39Z-
dc.date.available2019-02-18T15:46:39Z-
dc.date.issued2019en_US
dc.identifier.issn0049-0172en_US
dc.identifier.urihttp://hdl.handle.net/10553/54935-
dc.description.abstractObjectives: To identify patterns (clusters) of damage manifestation within a large cohort of juvenile SLE (jSLE) patients and evaluate their possible association with mortality. Methods: This is a multicentre, descriptive, cross-sectional study of a cohort of 345 jSLE patients from the Spanish Society of Rheumatology Lupus Registry. Organ damage was ascertained using the Systemic Lupus International Collaborating Clinics Damage Index. Using cluster analysis, groups of patients with similar patterns of damage manifestation were identified and compared. Results: Mean age (years) ± S.D. at diagnosis was 14.2 ± 2.89; 88.7% were female and 93.4% were Caucasian. Mean SLICC/ACR DI ± S.D. was 1.27 ± 1.63. A total of 12 (3.5%) patients died. Three damage clusters were identified: Cluster 1 (72.7% of patients) presented a lower number of individuals with damage (22.3% vs. 100% in Clusters 2 and 3, P < 0.001); Cluster 2 (14.5% of patients) was characterized by renal damage in 60% of patients, significantly more than Clusters 1 and 3 (P < 0.001), in addition to increased more ocular, cardiovascular and gonadal damage; Cluster 3 (12.7%) was the only group with musculoskeletal damage (100%), significantly higher than in Clusters 1 and 2 (P < 0.001). The overall mortality rate in Cluster 2 was 2.2 times higher than that in Cluster 3 and 5 times higher than that in Cluster 1 (P < 0.017 for both comparisons). Conclusions: In a large cohort of jSLE patients, renal and musculoskeletal damage manifestations were the two dominant forms of damage by which patients were sorted into clinically meaningful clusters. We found two clusters of jSLE with important clinical damage that were associated with higher rates of mortality, especially for the cluster of patients with predominant renal damage. Physicians should be particularly vigilant to the early prevention of damage in this subset of jSLE patients with kidney involvement.en_US
dc.languageengen_US
dc.publisher0049-0172
dc.relation.ispartofSeminars in Arthritis and Rheumatismen_US
dc.sourceSeminars in Arthritis and Rheumatism [ISSN 0049-0172], v. 48(6), p. 1025-1029en_US
dc.subject.otherCluster analysisen_US
dc.subject.otherJuvenile Systemic Lupus Erythematosusen_US
dc.subject.otherOrgan damage, Mortalityen_US
dc.subject.otherRELESSERen_US
dc.titleRelationship between damage and mortality in juvenile-onset systemic lupus erythematosus: Cluster analyses in a large cohort from the Spanish Society of Rheumatology Lupus Registry (RELESSER)en_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.semarthrit.2018.09.005en_US
dc.identifier.scopus85055050880-
dc.contributor.authorscopusid56823417100-
dc.contributor.authorscopusid37065040300-
dc.contributor.authorscopusid6602687781-
dc.contributor.authorscopusid6603553828-
dc.contributor.authorscopusid56268966400-
dc.contributor.authorscopusid6603414978-
dc.contributor.authorscopusid55258468600-
dc.contributor.authorscopusid6603550211-
dc.contributor.authorscopusid6507172289-
dc.contributor.authorscopusid56736884600-
dc.contributor.authorscopusid56487863000-
dc.contributor.authorscopusid6603487170-
dc.contributor.authorscopusid12782882100-
dc.contributor.authorscopusid57204237919-
dc.contributor.authorscopusid56488110900-
dc.contributor.authorscopusid7102430622-
dc.contributor.authorscopusid7103245648-
dc.contributor.authorscopusid56488005900-
dc.contributor.authorscopusid6603328312-
dc.contributor.authorscopusid6603560400-
dc.contributor.authorscopusid6603441345-
dc.contributor.authorscopusid6506910525-
dc.contributor.authorscopusid6701861584-
dc.contributor.authorscopusid55364424000-
dc.contributor.authorscopusid23111754100-
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.utils.revisionen_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr1,953
dc.description.jcr4,751
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
item.fulltextSin texto completo-
item.grantfulltextnone-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.fullNameHernández Beriain, José Ángel-
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