The impact of interferon beta and natalizumab on comorbid migraine in multiple sclerosis

Headache. 2012 Jul-Aug;52(7):1130-5. doi: 10.1111/j.1526-4610.2012.02146.x. Epub 2012 Apr 5.

Abstract

Background: Some multiple sclerosis (MS)-specific therapies may exacerbate a comorbid migraine. Whereas data regarding the impact of interferon beta (IFNB) on this comorbidity have been reported, studies on the role of natalizumab (NTZ) are still lacking.

Purpose: Our aim was to compare the impact of IFNB and NTZ on the frequency and disability of comorbid migraine in MS patients.

Methods: performed a longitudinal evaluation on MS patients with comorbid migraine previously assessed at our center and retested for the present study, by comparing data from 33 patients originally treated with IFNB and thereafter switched to NTZ vs 30 patients continued currently to receive IFNB.

Results: Longitudinal analysis showed a significant reduction of migraine frequency (from a mean value of 8.4 to 5.1 days per month; P = .034) and Migraine Disability Assessment Scale (MIDAS) score (from a mean value of 14.2 to 10.5; P = .045) in the subgroup patients switched from IFNB to NTZ but not in those remaining in the IFNB recipient, irrespective of level of fatigue, trait anxiety, depression, alexithymia, or other clinical variables.

Conclusions: Our findings suggest that NTZ did not exacerbate comorbid migraine in MS patients and support the hypothesis that IFNB might represent an important trigger for migraine worsening.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Antibodies, Monoclonal / therapeutic use
  • Antibodies, Monoclonal, Humanized / therapeutic use*
  • Comorbidity
  • Disability Evaluation
  • Female
  • Humans
  • Immunologic Factors / therapeutic use
  • Interferon-beta / therapeutic use*
  • Longitudinal Studies
  • Male
  • Migraine Disorders / drug therapy*
  • Migraine Disorders / epidemiology*
  • Multiple Sclerosis / epidemiology*
  • Natalizumab
  • Prevalence
  • Retrospective Studies
  • Treatment Outcome

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Immunologic Factors
  • Natalizumab
  • Interferon-beta