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