Abstract

Purpose: Familial Mediterranean fever (FMF) is the most common monogenic auto-inflammatory disease characterized by recurrent attacks of fever and serositis. It is associated with mutation in pyrin inflammasome leading to interleukin-1 (IL-1) over secretion. Although colchicine is the first line treatment in FMF, 5–10% of patients are reported in literature as non-responders. Colchicine is not always well-tolerated due either to its direct toxicity or to co-morbidities that preclude the administration of its proper dosage. For these patients an alternative or additional treatment to colchicine is necessary. This literature review reports the published data regarding the use of IL-1 inhibitors in Familial Mediterranean Fever.Results: There is no uniform definition of colchicine resistance, but the different studies of treatment with IL-1 inhibitors provide evidence of IL-1 pathogenic role in colchicine-resistant FMF. IL-1 inhibition is an efficacious option for controlling and preventing flares –at least at the short term- in FMF patients who are insufficiently controlled with colchicine alone. Although canakinumab is the only approved drug in Europe for colchicine resistant FMF treatment, experience with anakinra is also substantial. In the absence of comparative studies both treatments seem to be an equal option for the management of these patients. Overall the safety profile of IL-1 inhibitors seems not different in FMF patients than in the other diseases and can be considered as globally safe. The main side effects are local injection site reactions and infections.Conclusion: IL-1 inhibitors have the potential to improve patient outcome even in FMF patients with co-morbidities or severe complications in whom inflammation control is difficult to achieve with colchicine alone. Nevertheless, current data are limited and further evaluation of long-term efficacy and safety of IL-1 inhibitors are necessary, in order to provide robust evidence in this domain.

Highlights

  • Familial Mediterranean fever (FMF) is the most frequent monogenic auto-inflammatory disease

  • There is no uniform definition of colchicine resistance, but the different studies of treatment with IL-1 inhibitors provide evidence of IL-1 pathogenic role in colchicine-resistant FMF

  • IL-1 inhibition is an efficacious option for controlling and preventing flares –at least at the short term- in FMF patients who are insufficiently controlled with colchicine alone

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Summary

Introduction

Familial Mediterranean fever (FMF) is the most frequent monogenic auto-inflammatory disease. FMF is characterized by self-limited episodes fever associated to polyserositis and raised inflammatory markers [1]. The disease is mostly seen among particular ethnic groups such as patients with a Middle. Eastern ancestry or originating from the Mediterranean basin [2]. Autosomal recessive mutations in the MEFV gene are responsible for the symptoms in FMF [3, 4]. Its pathogenesis is not fully understood, pyrin is a crucial player in the regulation of innate immunity and FMF-associated missense mutations induce an uncontrolled IL-1 release [5]. Amyloid deposition and the development of end-stage renal disease are the most severe complications of FMF. Since 1972, colchicine is the cornerstone of treatment for FMF patients

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