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Clinical characteristics and genetic analyses of 187 patients with undifferentiated recurrent fever

Authors :
Ter Haar, Nienke
Eijkelboom, Charlotte
Cantarini, Luca
Papa, Riccardo
Brogan, Paul
Koné-Paut, Isabelle
Modesto, Consuelo
Hofer, Michael
Iaguru, Nicolae
Fingerhutová, Sárka
Insalaco, Antonella
Licciardi, Francesco
Uziel, Yosef
Jelušić, Marija
Nikishina, Irina
Nielsen, Susan
Papadopoulou-Alataki, Efimia
Olivieri, Alma Nunzia
Cimaz, Rolando
Susic, Gordana
Staņēviča, Valda
van Gijn, Marielle
Vitale, Antonio
Ruperto, Nicolino
Frenkel, Joost
Gattorno, Marco
Publication Year :
2019

Abstract

Objectives: To describe the clinical characteristics, treatment response and genetic findings in the largest cohort of patients with syndrome of undifferentiated recurrent fever (SURF). Methods: Clinical and genetic data from patients with SURF were extracted from the Eurofever registry, an international web-based registry that retrospectively collects clinical information on patients with autoinflammatory diseases. Results: In this study 202 patients were included. Seven patients had a chronic disease course, 195 patients had a recurrent disease course. The median age at disease onset was 4.6 years. Patients had a median of 12 episodes per year, with a median duration of 4 days. In 25 patients relatives were affected as well. Most commonly reported symptoms were arthralgia (n=125), myalgia (n=95), abdominal pain (n=98), fatigue (n=120), malaise (n=112), and mucocutaneous manifestations (n=139). In 17 patients genetic variants were found in autoinflammatory genes. These patients more often had affected relatives compared to patients without genetic variants (p=0.002). Most patients responded well to NSAIDs, corticosteroids, colchicine and anakinra. Complete remission was rarely achieved with NSAIDs alone. Notable patterns were found in patients with distinctive symptoms. Patients with pericarditis (n=12) were older at disease onset (32.3 years), and had fewer episodes per year (3.0/year) compared to other patients. Patients with an intellectual impairment (n=8) were younger at disease onset (2.2 years) and often had relatives affected (28.6%). Conclusion: This study describes the clinical characteristics in the largest cohort of SURF patients. Patients with genetic variants found more often had relatives affected.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.57a035e5b1ae..9aa173f0ed5835f1081271ac2bb95345