Ibudilast in relapsing-remitting multiple sclerosis A neuroprotectant?

被引:118
作者
Barkhof, F. [1 ]
Hulst, H. E.
Drulovic, J. [3 ]
Uitdehaag, B. M. J. [2 ]
Matsuda, K. [4 ]
Landin, R. [4 ]
机构
[1] Vrije Univ Amsterdam, Med Ctr, Dept Radiol, Image Anal Ctr, NL-1007 MB Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Med Ctr, MS Ctr, NL-1007 MB Amsterdam, Netherlands
[3] Inst Neurol Beograd, Klin Ctr Srbije, Belgrade, Serbia
[4] Medicinova Inc, San Diego, CA USA
关键词
EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; PHOSPHODIESTERASE INHIBITOR; LOVASTATIN; MICROGLIA; PROTECTS; DISEASE; DAMAGE; MODEL;
D O I
10.1212/WNL.0b013e3181d7d651
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Ibudilast is a phosphodiesterase inhibitor influencing inflammation and neurodegeneration in multiple sclerosis (MS). This study evaluated the safety, tolerability, and effects on MRI parameters of 2 different doses of ibudilast in relapsing forms of MS. Methods: In this multicenter, double-blind, phase 2 trial, patients with relapsing MS and gadolinium-enhancing lesions were randomly assigned 1:1:1 to receive 30 or 60 mg ibudilast or placebo every day for 12 months. The primary endpoint was the cumulative number of newly active lesions on bimonthly brain MRI over 12 months. Secondary endpoints included relapse rate, change in Expanded Disability Status Scale (EDSS) score, T2-hyperintense and T1-hypointense lesion volumes, and percent brain volume change (PBVC). Results: A total of 297 patients were randomized in 19 centers. During the first 12 months, the mean number of active lesions and relapse rate did not differ between treatment arms. A reduction in PBVC (p = 0.04) was found in the 60-mg group (0.8%) compared with placebo (1.2%). Post hoc analysis showed a reduction in the proportion active lesions that evolved into persistent black holes for the 60-mg (0.14; p = 0.004) and 30-mg (0.17; p = 0.036) groups compared with the placebo group (0.24). Over 2 years, there were fewer patients (p = 0.026) with confirmed progression on the EDSS. Treatment with ibudilast was generally safe and well tolerated. Conclusion: Ibudilast showed no beneficial effect on the rate of newly active lesions and relapses. However, preliminary evidence suggests that ibudilast seems to act in a neuroprotective fashion as measured by 2 independent MRI outcomes, with a possible beneficial clinical effect on disability progression. Classification of evidence:This interventional study provides Class III evidence on the effect of ibudilast on disease activity. Neurology (R) 2010; 74:1033-1040
引用
收藏
页码:1033 / 1040
页数:8
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