Author:
Yagishita Mizuki,Tsuboi Hiroto,Kuroda Yuki,Sawabe Tomonori,Kawashima Akira,Kawashima Fumina,Uematsu Nana,Sato Ryota,Nishiyama Taihei,Terasaki Mayu,Toko Hirofumi,Honda Fumika,Ohyama Ayako,Abe Saori,Kitada Ayako,Miki Haruka,Hagiwara Shinya,Kondo Yuya,Sumida Takayuki,Matsumoto Isao
Abstract
AbstractRecent studies have suggested that the clinical features of elderly-onset adult-onset Still’s disease (AOSD) differ from those of young and middle-aged-onset patients, whereas the details remain unclear, and cytokine profiles of elderly-onset AOSD have not been reported. To clarify the clinical features and cytokine profiles of elderly-onset AOSD, we examined patients with AOSD who developed the disease between January 2006 and September 2021. We divided the patients into the young and middle-aged-onset group (aged < 65 years) and the elderly-onset group (aged ≥ 65 years) and compared the groups in terms of patient characteristics, clinical symptoms, laboratory findings including serum interleukin (IL)-6 and IL-18, treatment, and prognosis. A total of 48 patients were examined (10 in the elderly-onset group). In the elderly-onset group, atypical rash was significantly more frequent, typical rash and splenomegaly were significantly less frequent, white blood cell count and neutrophil ratio were significantly higher and serum IL-6 levels were significantly lower. Serum IL-6 showed a significantly negative correlation with age at onset. Treatment and relapse were comparable between the 2 groups, whereas infections were significantly more frequent in the elderly-onset group. The clinical features and cytokine profiles of elderly-onset AOSD might differ from those of young and middle-aged-onset AOSD.
Publisher
Springer Science and Business Media LLC
Cited by
3 articles.
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