4.0 Article

ω-3 Fatty Acid Treatment in Multiple Sclerosis (OFAMS Study) A Randomized, Double-Blind, Placebo-Controlled Trial

Journal

ARCHIVES OF NEUROLOGY
Volume 69, Issue 8, Pages 1044-1051

Publisher

AMER MEDICAL ASSOC
DOI: 10.1001/archneurol.2012.283

Keywords

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Funding

  1. Merck-Serono
  2. Novartis
  3. Biogen Idec
  4. sanofi-aventis
  5. AstraZeneca
  6. Bayer Schering Pharma AG
  7. GlaxoSmithKline
  8. Merck Serono
  9. Western Norway Regional Health Authority
  10. Norwegian Multiple Sclerosis Society
  11. Pronova Biocare
  12. Amersham Health, Norway
  13. Merck-Serono, Norway

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Objective: To investigate whether omega-3 fatty acids reduce magnetic resonance imaging (MRI) and clinical disease activity in patients with multiple sclerosis, both as monotherapy and in combination with interferon beta-1a treatment. Design: Multicenter, randomized, double-blind, placebo-controlled clinical trial conducted from 2004 to 2008. Setting: Thirteen public neurology departments in Norway. Participants: Patients aged 18 to 55 years with active relapsing-remitting multiple sclerosis, with a disability score equivalent to 5.0 or less on the Kurtzke Expanded Disability Status Scale. Ninety-two patients were randomized to omega-3 fatty acids (n = 46) or placebo capsules (n = 46). Interventions: Administration of 1350 mg of eicosapentaenoic acid and 850 mg of docosahexaenoic acid daily or placebo. After 6 months, all patients in addition received subcutaneously 44 mu g of interferon beta-1a 3 times per week for another 18 months. Main Outcome Measure: The primary outcome measure was MRI disease activity as measured by the number of new T1-weighted gadolinium-enhancing lesions during the first 6 months. Secondary outcome measures included MRI disease activity after 9 months and 24 months, relapse rate, disability progression, fatigue, quality of life, and safety. Results: The cumulative number of gadolinium-enhancing MRI lesions during the first 6 months were similar in the omega-3 fatty acids and placebo groups (median difference, 1; 95% CI, 0 to 3; P =. 09). No difference in relapse rate was detected after 6 (median difference, 0; 95% CI, 0 to 0; P =. 54) or 24 (median difference, 0; 95% CI, 0 to 0; P =. 72) months. The proportion of patients without disability progression was 70% in both groups (P > .99). No differences were detected in fatigue or quality-of-life scores, and no safety concerns appeared. Serum analyses of fatty acids showed an increase in omega-3 fatty acids (mean difference, 7.60; 95% CI, 5.57 to 7.91; P < .001) in the patients treated with omega-3 fatty acids compared with the placebo group. Conclusion: No beneficial effects on disease activity were detected from omega-3 fatty acids when compared with placebo as monotherapy or in combination with interferon beta-1a. Magnetic resonance imaging disease activity was reduced as expected by interferon beta-1a.

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