Abstract
Colchicine is the treatment of choice in familial Mediterranean fever (FMF) for the prevention of both attacks and secondary amyloidosis. The overall nonresponder rate is about 5-10%. Anakinra is known to have good effectiveness in a severe autoinflammatory syndrome [chronic infantile neurological cutaneous and articular (CINCA) syndrome] and other recurrent hereditary periodic fevers. Pyrin-the protein involved in FMF-has a role in activating the proinflammatory cytokine interleukin (IL)-1β. We report the effectiveness of the addition of an IL-1-receptor inhibitor (anakinra) to colchicine in controlling the febrile attacks and acute phase response in an adolescent with FMF resistant to colchicine.
Original language | English |
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Pages (from-to) | 695-696 |
Number of pages | 2 |
Journal | European Journal of Pediatrics |
Volume | 167 |
Issue number | 6 |
DOIs | |
Publication status | Published - Jun 2008 |
Keywords
- Anakinra
- Colchicine resistance
- Familial Mediterranean fever
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health