Atorvastatin added to interferon beta for relapsing multiple sclerosis: a randomized controlled trial
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BORIS DOI
Date of Publication
2012
Publication Type
Article
Division/Institute
Author
Humpert, Sebastian | |
von Bredow, Ferdinand | |
Schwegler, Guido | |
Schött, Dagmar | |
Müller, Martin | |
Goebels, Norbert | |
Müller, Felix | |
Tettenborn, Barbara | |
Kappos, Ludwig | |
Naegelin, Yvonne |
Series
Journal of neurology
ISSN or ISBN (if monograph)
0340-5354
Publisher
Springer-Verlag
Language
English
Publisher DOI
PubMed ID
22569835
Description
Statins have anti-inflammatory and immunomodulatory properties in addition to lipid-lowering effects. The present study evaluated the effect of atorvastatin added to interferon beta-1b in multiple sclerosis (MS) in a multicenter, randomized, parallel-group, rater-blinded study performed in eight Swiss hospitals. Seventy-seven patients with relapsing-remitting MS started interferon beta-1b every other day. After 3 months, they were randomized 1:1 to receive atorvastatin 40 mg/day or not in addition to interferon beta-1b until month 15. The primary endpoint was the proportion of patients with new lesions on T2-weighted images at month 15 compared to baseline at month three. At study end, the proportion of patients with new lesions on T2-weighted images was equal in both groups (odds ratio 1.14; 95 % CI 0.36-3.56; p = 0.81). All predefined secondary endpoints including number of new lesions and total lesion volume on T2-weighted images, total number of new Gd-enhancing lesions on T1-weighted images, total brain volume, volume of grey matter, volume of white matter, EDSS, MSFC, relapse rate, time to first relapse, number of relapse-free patients and neutralizing antibodies did not show any significant differences (all p values >0.1). Transient elevations of liver enzymes were more frequent with atorvastatin (p = 0.02). In conclusion, atorvastatin 40 mg/day in addition to interferon beta-1b did not have a beneficial effect on relapsing-remitting MS compared to interferon beta-1b monotherapy over a 12-month period.
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415_2012_Article_6513.pdf | text | Adobe PDF | 250.82 KB | Attribution (CC BY 4.0) | published |