Pregled bibliografske jedinice broj: 1013042
Clinical characteristics and genetic analyses of 187 patients with undefined autoinflammatory diseases
Clinical characteristics and genetic analyses of 187 patients with undefined autoinflammatory diseases // Annals of the rheumatic diseases, 78 (2019), 1405-1411 doi:10.1136/annrheumdis-2018-214472 (međunarodna recenzija, članak, znanstveni)
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Naslov
Clinical characteristics and genetic analyses of 187 patients with undefined autoinflammatory diseases
Autori
Ter Haar, Nienke M ; Eijkelboom, Charlotte ; Cantarini, Luca ; Papa, Riccardo ; Brogan, Paul A ; Kone-Paut, Isabelle ; Modesto, Consuelo ; Hofer, Michael ; Iagaru, Nicolae ; Fingerhutová, Sárka ; Insalaco, Antonella ; Licciardi, Francesco ; Uziel, Yosef ; Jelusic, Marija ; Nikishina, Irina ; Nielsen, Susan ; Papadopoulou-Alataki, Efimia ; Olivieri, Alma Nunzia ; Cimaz, Rolando ; Susic, Gordana ; Stanevica, Valda ; van Gijn, Marielle ; Vitale, Antonio ; Ruperto, Nicolino ; Frenkel, Joost ; Gattorno, Marco
Kolaboracija
Paediatric Rheumatology International Trials Organisation (PRINTO)
Izvornik
Annals of the rheumatic diseases (0003-4967) 78
(2019);
1405-1411
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
autoinflammatory diseases ; eurofever ; inflammation ; recurrent fever
Sažetak
OBJECTIVES: To describe the clinical characteristics, treatment response and genetic findings in a large cohort of patients with undefined systemic autoinflammatory diseases (SAIDs). METHODS: Clinical and genetic data from patients with undefined SAIDs were extracted from the Eurofever registry, an international web-based registry that retrospectively collects clinical information on patients with autoinflammatory diseases. RESULTS: This study included 187 patients. Seven patients had a chronic disease course, 180 patients had a recurrent disease course. The median age at disease onset was 4.3 years. Patients had a median of 12 episodes per year, with a median duration of 4 days. Most commonly reported symptoms were arthralgia (n=113), myalgia (n=86), abdominal pain (n=89), fatigue (n=111), malaise (n=104) and mucocutaneous manifestations (n=128). In 24 patients, relatives were affected as well. In 15 patients, genetic variants were found in autoinflammatory genes. Patients with genetic variants more often had affected relatives compared with patients without genetic variants (p=0.005). Most patients responded well to non- steroidal anti-inflammatory drugs (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=11) were older at disease onset (33.8 years) and had fewer episodes per year (3.0/year) compared with 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 of a large cohort of patients with undefined SAIDs. Among these, patients with pericarditis and intellectual impairment appear to comprise distinct subsets.
Izvorni jezik
Engleski
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE