Alcohol, coffee, fish, smoking and disease progression in multiple sclerosis
Version of Record online: 25 NOV 2011
© 2011 The Author(s). European Journal of Neurology © 2011 EFNS
European Journal of Neurology
Volume 19, Issue 4, pages 616–624, April 2012
How to Cite
D’hooghe, M. B., Haentjens, P., Nagels, G. and De Keyser, J. (2012), Alcohol, coffee, fish, smoking and disease progression in multiple sclerosis. European Journal of Neurology, 19: 616–624. doi: 10.1111/j.1468-1331.2011.03596.x
- Issue online: 14 MAR 2012
- Version of Record online: 25 NOV 2011
- Received 24 May 2011 Accepted 20 October 2011
- multiple sclerosis;
Background: Certain lifestyle factors might influence disease activity in multiple sclerosis (MS).
Objectives: To investigate the consumption of alcoholic beverages, caffeinated drinks, fish and cigarette smoking in relation to disability progression in relapsing onset and progressive onset MS.
Methods: We conducted a cross-sectional survey amongst individuals with MS, registered by the Flemish MS society in Belgium. A time-to-event analysis and Cox proportional-hazard regression were performed with time to Expanded Disability Status Scale (EDSS) 6 (requiring a cane or support to walk for a distance of 100 m) as outcome measure. Hazard ratios for the time from onset and from birth were adjusted for age at onset, gender and immunomodulatory treatment.
Results: Data of 1372 persons with definite MS were collected. In the relapsing onset group, a decreased risk for reaching EDSS 6 was found in regular consumers of alcohol, wine, coffee and fish compared with those who never consumed these substances. Cigarette smoking was associated with an enhanced risk for reaching EDSS 6. In the progressive onset group, no association with the risk of reaching EDSS 6 was found, except for the type of fish. Preference for fatty fish was associated with an increased risk to reach EDSS 6, when lean fish was taken as the reference category.
Conclusion: Consumption of alcoholic beverages, coffee and fish were inversely associated with progression of disability in relapsing onset MS, but not in progressive onset MS. These findings allow to support the hypothesis that different mechanisms might underlie progression of disability in relapsing and progressive onset MS.