Publication:
Still's disease continuum from childhood to elderly: data from the international AIDA Network Still's disease registry

dc.contributor.authorALİBAZ ÖNER, FATMA
dc.contributor.authorsVitale A., Caggiano V., Lopalco G., Mayrink Giardini H. A., Ciccia F., Almaghlouth I. A., Ruscitti P., Sfikakis P. P., Tufan A., Dagna L., et al.
dc.date.accessioned2023-12-12T06:20:52Z
dc.date.accessioned2026-01-11T17:15:46Z
dc.date.available2023-12-12T06:20:52Z
dc.date.issued2023-12-01
dc.description.abstractObjective Still’s disease is more frequently observed in the paediatric context, but a delayed onset is not exceptional both in the adulthood and in the elderly. However, whether paediatric-onset, adult-onset and elderly-onset Still’s disease represent expressions of the same disease continuum or different clinical entities is still a matter of controversy. The aim of this study is to search for any differences in demographic, clinical features and response to treatment between pediatric-onset, adultonset and elderly-onset Still’s disease. Methods Subjects included in this study were drawn from the International AutoInflammatory Disease Alliance Network registry for patients with Still’s disease. Results A total of 411 patients suffering from Still’s disease were enrolled; the disease occurred in the childhood in 65 (15.8%) patients, in the adult 314 (76.4%) patients and in the elderly in 32 (7.8%) patients. No statistically significant differences at post-hoc analysis were observed in demographic features of the disease between pediatric-onset, adult-onset and elderly-onset Still’s disease. The salmon-coloured skin rash (p=0.004), arthritis (p=0.009) and abdominal pain (p=0.007) resulted significantly more frequent among paediatric patients than in adult cases, while pleuritis (p=0.015) and arthralgia (p<0.0001) were significantly more frequent among elderly-onset patients compared with paediatric-onset subjects. Regarding laboratory data, thrombocytosis was significantly more frequent among paediatric patients onset compared with adult-onset subjects (p<0.0001), while thrombocytopenia was more frequent among elderlyonset patients although statistical significance was only bordered. No substantial differences were observed in the response to treatments. Conclusions Despite some minor difference between groups, overall, demographic, clinical, laboratory and treatments aspects of Still’s disease were similarly
dc.identifier.citationVitale A., Caggiano V., Lopalco G., Mayrink Giardini H. A., Ciccia F., Almaghlouth I. A., Ruscitti P., Sfikakis P. P., Tufan A., Dagna L., et al., "Still's disease continuum from childhood to elderly: data from the international AIDA Network Still's disease registry.", RMD open, cilt.9, sa.4, 2023
dc.identifier.doi10.1136/rmdopen-2023-003578
dc.identifier.issue4
dc.identifier.urihttps://avesis.marmara.edu.tr/api/publication/ca167ee9-d967-4fc4-9db5-69f4941702a5/file
dc.identifier.urihttps://hdl.handle.net/11424/295550
dc.identifier.volume9
dc.language.isoeng
dc.relation.ispartofRMD open
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleStill's disease continuum from childhood to elderly: data from the international AIDA Network Still's disease registry
dc.typearticle
dspace.entity.typePublication

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