Familial Mediterranean Fever and Multiple Sclerosis Successfully Treated With Interferon Beta-1a: A Case Report

Bilgin Öztürk1

  • 1Department of Neurology, Gülhane Training and Research Hospital, Ankara, Turkey.

Archives of Rheumatology
|February 4, 2020
PubMed

Insights

This case study highlights a patient with multiple sclerosis (MS) and familial Mediterranean fever (FMF). Interferon beta-1a treatment for MS unexpectedly resolved FMF attacks, suggesting a potential new therapeutic avenue.

Area of Science:

  • Neuroimmunology
  • Rheumatology
  • Genetics

Background:

  • Multiple Sclerosis (MS) is a leading cause of demyelinating disease in Turkey.
  • Familial Mediterranean Fever (FMF) is the most prevalent periodic fever syndrome globally.
  • Co-occurrence of MS and FMF presents unique clinical and therapeutic challenges.

Observation:

  • A 37-year-old male with a 27-year history of colchicine-treated FMF experienced persistent, severe monthly attacks.
  • The patient was diagnosed with MS, necessitating treatment with Interferon (IFN) beta-1a.
  • Neurological and systemic evaluations confirmed the diagnoses.

Findings:

  • Following initiation of subcutaneous IFN beta-1a for MS, the patient ceased experiencing FMF attacks.
  • The patient remained free of FMF attacks for 12 months after discontinuing colchicine.
  • IFN beta-1a, a standard MS therapy, is not typically used for FMF.

Implications:

  • IFN beta-1a may offer a novel therapeutic option for patients with coexisting MS and FMF.
  • This finding suggests potential benefits for colchicine-resistant FMF patients.
  • Further systematic clinical studies are warranted to validate IFN beta's efficacy in dual-diagnosis patients.

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