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

Authors :
Vitale A
Caggiano V
Lopalco G
Mayrink Giardini HA
Ciccia F
Almaghlouth IA
Ruscitti P
Sfikakis PP
Tufan A
Dagna L
Giacomelli R
Hinojosa-Azaola A
Ragab G
Direskeneli H
Fotis L
Sota J
Iannone F
Morrone M
de Brito Antonelli IP
Dagostin MA
Iacono D
Patrone M
Asfina K
Alanazi F
Di Cola I
Gaggiano C
Tektonidou MG
Kardas RC
Kucuk H
Campochiaro C
Tomelleri A
Navarini L
Berardicurti O
Martín-Nares E
Torres-Ruiz J
Mahmoud AAA
Alibaz-Oner F
Kourtesi K
Tarsia M
Sfriso P
Makowska J
Govoni M
La Torre F
Maggio MC
Monti S
Del Giudice E
Emmi G
Bartoloni E
Hernández-Rodríguez J
Gómez-Caverzaschi V
Maier A
Simonini G
Iagnocco A
Conti G
Olivieri AN
De Paulis A
Lo Gullo A
Viapiana O
Wiesik-Szewczyk E
Erten S
Ogunjimi B
Carubbi F
Tharwat S
Laskari K
Costi S
Triggianese P
Karamanakos A
Conforti A
Frassi M
Sebastiani GD
Gidaro A
Mauro A
Balistreri A
Fabiani C
Frediani B
Cantarini L
Source :
RMD open [RMD Open] 2023 Dec 01; Vol. 9 (4). Date of Electronic Publication: 2023 Dec 01.
Publication Year :
2023

Abstract

Objective: 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, adult-onset and elderly-onset Still's disease.<br />Methods: Subjects included in this study were drawn from the International AutoInflammatory Disease Alliance Network registry for patients with Still's disease.<br />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 elderly-onset patients although statistical significance was only bordered. No substantial differences were observed in the response to treatments.<br />Conclusions: Despite some minor difference between groups, overall, demographic, clinical, laboratory and treatments aspects of Still's disease were similarly observed in patients at all ages. This supports that pediatric-onset, adult-onset and elderly-onset Still's disease is the same clinical condition arising in different ages.<br />Competing Interests: Competing interests: None declared.<br /> (© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.)

Details

Language :
English
ISSN :
2056-5933
Volume :
9
Issue :
4
Database :
MEDLINE
Journal :
RMD open
Publication Type :
Academic Journal
Accession number :
38053457
Full Text :
https://doi.org/10.1136/rmdopen-2023-003578