Adult-onset Still’s disease: an Italian multicentre retrospective observational study of manifestations and treatments in 245 patients

Paolo Sfriso, Roberta Priori, Guido Valesini, Silvia Rossi, Carlo Maurizio Montecucco, Anna D’Ascanio, Linda Carli, Stefano Bombardieri, Gaetana LaSelva, Florenzo Iannone, Giovanni Lapadula, Stefano Alivernini, Gianfranco Ferraccioli, Michele Colaci, Clodoveo Ferri, Daniela Iacono, Gabriele Valentini, Luisa Costa, Raffaele Scarpa, Andrea LoMonacoValentina Bagnari, Marcello Govoni, Ilaria Piazza, Silvano Adami, Francesco Ciccia, Giovanni Triolo, Elisa Alessandri, Maurizio Cutolo, Luca Cantarini, Mauro Galeazzi, Piero Ruscitti, Roberto Giacomelli, Francesco Caso, Paola Galozzi, Leonardo Punzi

Research output: Contribution to journalArticle

Abstract

Adult-onset Still’s disease (AOSD) is a systemic inflammatory condition of unknown aetiology characterized by typical episodes of spiking fever, evanescent rash, arthralgia, leukocytosis and hyperferritinemia. Given the lack of data in Italian series, we promote a multicentric data collection to characterize the clinical phenotype of Italian patients with AOSD. Data from 245 subjects diagnosed with AOSD were collected by 15 centres between March and May 2013. The diagnosis was made following Yamaguchi’s criteria. Data regarding clinical manifestations, laboratory features, disease course and treatments were reported and compared with those presented in other published series of different ethnicity. The most frequent features were the following: arthritis (93 %), pyrexia (92.6 %), leukocytosis (89 %), negative ANA (90.4 %) and neutrophilia (82 %). As compared to other North American, North European, Middle Eastern and Far Eastern cohorts, Italian data show differences in clinical and laboratory findings. Regarding the treatments, in 21.9 % of cases, corticosteroids and traditional DMARDs have not been able to control the disease while biologics have been shown to be effective in 48 to 58 patients. This retrospective work summarizes the largest Italian multicentre series of AOSD patients and presents clinical and laboratory features that appear to be influenced by the ethnicity of the affected subjects.

Original languageEnglish
Pages (from-to)1683-1689
Number of pages7
JournalClinical Rheumatology
Volume35
Issue number7
DOIs
Publication statusPublished - Jul 1 2016

Keywords

  • Adult-onset Still’s disease
  • Biologic drugs
  • Clinical presentation
  • Laboratory findings
  • Retrospective study

ASJC Scopus subject areas

  • Rheumatology
  • Medicine(all)

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    Sfriso, P., Priori, R., Valesini, G., Rossi, S., Montecucco, C. M., D’Ascanio, A., Carli, L., Bombardieri, S., LaSelva, G., Iannone, F., Lapadula, G., Alivernini, S., Ferraccioli, G., Colaci, M., Ferri, C., Iacono, D., Valentini, G., Costa, L., Scarpa, R., ... Punzi, L. (2016). Adult-onset Still’s disease: an Italian multicentre retrospective observational study of manifestations and treatments in 245 patients. Clinical Rheumatology, 35(7), 1683-1689. https://doi.org/10.1007/s10067-016-3308-8