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视神经脊髓炎和多发性硬化患者对干扰素 β-1b 治疗的不同反应。

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

机构信息

Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan.

出版信息

Eur J Neurol. 2010 May;17(5):672-6. doi: 10.1111/j.1468-1331.2009.02897.x. Epub 2009 Dec 21.

Abstract

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.

摘要

背景

虽然复发缓解型多发性硬化症(MS)的治疗获益已得到明确证实,但干扰素β-1b(IFNB-1b)治疗视神经脊髓炎(NMO)是否有效仍存在争议。

方法

我们回顾了 18 例复发型 NMO 患者接受 IFNB-1b 治疗的反应,并将结果与 38 例复发缓解型 MS 患者进行了比较。我们比较了 NMO 和 MS 患者的临床特征、年复发率(ARR)以及接受 IFNB-1b 治疗前后无复发的概率。

结果

IFNB-1b 治疗后 ARR 增加超过 50%的患者比例在 NMO 中明显高于 MS(P=0.046)。MS 患者接受 IFNB-1b 治疗后 ARR 明显低于治疗前(P=0.015),但 NMO 患者并非如此。Kaplan-Meier 和对数秩统计分析显示,IFNB-1b 治疗后 NMO 的无复发率低于 MS(P=0.032)。分析还显示,MS 在 IFNB-1b 治疗前的无复发率低于治疗后的无复发率(P<0.001),但 NMO 并非如此。

结论

IFNB-1b 治疗似乎对预防 NMO 复发无效,可能是因为 NMO 和 MS 的免疫发病机制存在差异。

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