Different responses to interferon beta-1b treatment in patients with neuromyelitis optica and multiple sclerosis

被引:88
作者
Uzawa, A. [1 ]
Mori, M. [1 ]
Hayakawa, S. [1 ]
Masuda, S. [1 ]
Kuwabara, S. [1 ]
机构
[1] Chiba Univ, Grad Sch Med, Dept Neurol, Chuo Ku, Chiba 2608670, Japan
关键词
antiaquaporin-4; antibody; interferon beta-1b; multiple sclerosis; neuromyelitis optica; relapse; treatment; WATER CHANNEL; PATHOGENESIS; MECHANISMS; JAPANESE; THERAPY; LESIONS;
D O I
10.1111/j.1468-1331.2009.02897.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Although the benefit of treatment for relapsing-remitting multiple sclerosis (MS) is firmly established, whether interferon beta-1b (IFNB-1b) therapy is efficacious for neuromyelitis optica (NMO) has been debated. Methods: We reviewed the responses to IFNB-1b treatment in 18 patients with relapsing NMO and compared the results with those from 38 patients with relapsing-remitting MS. We compared clinical characteristics, the annualized relapse rate (ARR) and the probability of being relapse free before and after IFNB-1b treatment in patients with NMO and MS. Results: The proportion of patients with more than 50% increase in the ARR after IFNB-1b treatment was much higher in NMO than in MS (P = 0.046). ARR was significantly lower in patients with MS after IFNB-1b administration than before (P = 0.015), but not in NMO. Kaplan-Meier and log-rank statistical analyses revealed that relapse-free rates were lower in NMO than MS after IFNB-1b treatment (P = 0.032). The analyses also showed lower relapse-free rates during the pre-IFNB-1b treatment period than the post-IFNB-1b treatment period in MS (P < 0.001), but not in NMO. Conclusion: IFNB-1b treatment does not appear to be effective for preventing relapse in NMO likely because of differences between the immune-pathogenesis of NMO and MS.
引用
收藏
页码:672 / 676
页数:5
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