Cluster analysis of paediatric Behcet's disease: Data from The Pediatric Rheumatology Academy-Research Group

dc.authorid0000-0003-2575-6309
dc.authorid0000-0003-0466-0228
dc.authorid0000-0001-5637-8553
dc.contributor.authorDemir, Ferhat
dc.contributor.authorSonmez, Hafize Emine
dc.contributor.authorBaglan, Esra
dc.contributor.authorAkgun, Ozlem
dc.contributor.authorCoskuner, Taner
dc.contributor.authorYener, Gulcin Otar
dc.contributor.authorOzturk, Kubra
dc.date.accessioned2025-05-10T19:38:42Z
dc.date.issued2023
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractObjectives Behcet's disease (BD) is a systemic vasculitis affecting many organ systems, with the involvement of all-sized arteries and veins. The study aims to determine the main characteristics of paediatric BD patients and also analyse the clustering phenotypes. Methods Demographic data, clinical manifestations, laboratory features, treatment schedules, and disease outcomes were achieved from patients' charts retrospectively. A cluster analysis was performed according to the phenotype. Results A total of 225 (109 male/116 female) patients with BD were enrolled in the study. The median ages of disease onset and diagnosis were 131 (36-151) and 156 (36-192) months, respectively. According to cluster analysis, 132 (58.6%) patients belonged to the mucocutaneous-only cluster (C1), while 35 (15.6%) patients fitted to articular type (C2), 25 (11.1%) were in the ocular cluster (C3), 26 (11.6%) were in the vascular cluster (C4), and 7(3.1%) belonged to the gastrointestinal cluster (C5). Ocular and vascular clusters were more common in boys (p < .001), while girls usually presented with the mucocutaneous-only cluster. The disease activity at the diagnosis and the last control was higher in ocular, vascular, and gastrointestinal clusters. Conclusions These identified juvenile BD clusters express different phenotypes with different outcomes Our analysis may help clinicians to identify the disease subtypes accurately and to arrange personalized treatment.
dc.identifier.doi10.1093/mr/roac044
dc.identifier.endpage578
dc.identifier.issn1439-7595
dc.identifier.issn1439-7609
dc.identifier.issue3
dc.identifier.pmid35534229
dc.identifier.scopus2-s2.0-85144188371
dc.identifier.scopusqualityQ2
dc.identifier.startpage574
dc.identifier.urihttps://doi.org/10.1093/mr/roac044
dc.identifier.urihttps://hdl.handle.net/20.500.14730/9446
dc.identifier.volume33
dc.identifier.wosWOS:000803493000001
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherOxford Univ Press
dc.relation.ispartofModern Rheumatology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.subjectJuvenile Behcet's disease
dc.subjectcluster analysis
dc.subjectBehcet's disease
dc.titleCluster analysis of paediatric Behcet's disease: Data from The Pediatric Rheumatology Academy-Research Group
dc.typeArticle

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