| Literature DB >> 29450637 |
Fatma Yazılıtaş1, Özlem Aydoğ2, Sare Gülfem Özlü3, Evrim Kargın Çakıcı4, Tülin Güngör5, Fehime Kara Eroğlu5, Gökçe Gür5, Mehmet Bülbül5.
Abstract
Familial Mediterranean fever (FMF), the most common hereditary autoinflammatory disorder is characterized by recurrent episodes of fever, serositis, arthritis. The major long-term result is amyloidosis. Colchicine remains the principle of the treatment; it not only prevents the acute attacks but also prevents the long-term complications such as amyloidosis; 5-10% of the patients are unresponsive to treatment. Recently new therapeutic options as anti-interleukin 1 agents are successfully used for the patients who do not respond to colchicine treatment. In this study, we retrospectively evaluated 11 pediatric colchicine-resistant FMF patients who were treated with canakinumab. Three of the patients had amyloidosis and two had uveitis. Based on our results, we suggest that canakinumab may be a safe and effective therapy in patients who are resistant to colchicine and even in the patients with amyloidosis. We also suggest that canakinumab might be a safe option for the patients with uveitis.Entities:
Keywords: Amyloidosis; Canakinumab; Childhood; Familial Mediterranean fever; Uveitis
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Year: 2018 PMID: 29450637 DOI: 10.1007/s00296-018-3993-5
Source DB: PubMed Journal: Rheumatol Int ISSN: 0172-8172 Impact factor: 2.631