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.
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 MSpatients. METHODS: performed a longitudinal evaluation on MSpatients 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 MSpatients and support the hypothesis that IFNB might represent an important trigger for migraine worsening.
Authors: Robert W Foley; Nathan T Tagg; Matthew K Schindler; Kaylan M Fenton; Daniel S Reich; Irene Cortese; Ellen M Mowry Journal: Mult Scler Date: 2017-06-22 Impact factor: 6.312
Authors: Hilda J I de Jong; Elaine Kingwell; Afsaneh Shirani; Jan Willem Cohen Tervaert; Raymond Hupperts; Yinshan Zhao; Feng Zhu; Charity Evans; Mia L van der Kop; Anthony Traboulsee; Paul Gustafson; John Petkau; Ruth Ann Marrie; Helen Tremlett Journal: Neurology Date: 2017-05-12 Impact factor: 9.910