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首页> 外文期刊>Multiple sclerosis: clinical and laboratory research >Intramuscular interferon beta-1a is effective in Japanese patients with relapsing-remitting multiple sclerosis: A pre-treatment versus treatment comparison study of gadolinium-enhanced MRI brain lesions
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Intramuscular interferon beta-1a is effective in Japanese patients with relapsing-remitting multiple sclerosis: A pre-treatment versus treatment comparison study of gadolinium-enhanced MRI brain lesions

机译:肌内干扰素β-1a在日本复发缓解型多发性硬化症患者中有效:versus增强MRI脑损伤的治疗前与治疗比较研究

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摘要

Background and objective: Interferon beta (IFNβ) is standard therapy for multiple sclerosis (MS). The efficacy of intramuscular (IM) IFNβ-1a (AVONEX?) was assessed in 25 Japanese patients with relapsingremitting MS (RRMS). Methods: Patients with RRMS not previously treated with IFNβ or other disease-modifying therapies were included in this 36-week study. The primary outcome was the average total number of gadolinium-enhanced lesions detected on four brain MRI scans during the last 12 weeks of 24 weeks treatment with IM IFNβ-1a 30 μg once weekly compared with the number during the 12-week pre-treatment period. Lesions were counted by blinded investigators. Results: IM IFNβ-1a significantly decreased the median number of gadolinium-enhanced lesions from 2.5 to 0.3 (p ≤ 0.0001) compared with pre-treatment values. The median number of new gadolinium-enhanced lesions also decreased significantly from 2.0 to 0.3 (p = 0.0002). Serum neopterin was induced in a manner similar to that observed previously in a Caucasian RRMS population. No new adverse events occurred during the study. Conclusion: This first study of IM IFNβ-1a in Japanese patients with RRMS demonstrated a level of efficacy similar to that reported in Caucasian patients based on an assessment of pre-treatment and post-treatment gadolinium-enhanced lesions.
机译:背景与目的:干扰素β(IFNβ)是多发性硬化症(MS)的标准疗法。在25例日本复发性MS患者(RRMS)中评估了肌内(IM)IFNβ-1a(AVONEX?)的疗效。方法:这项为期36周的研究纳入了先前未接受过IFNβ或其他疾病缓解疗法治疗的RRMS患者。主要结局是在每周一次用IMIFNβ-1a30μg治疗的24周的最后12周内,通过四次脑部MRI扫描发现的g增强病变的平均总数,与治疗前12周的次数相比。盲人的调查员对病变进行计数。结果:与治疗前相比,IMIFNβ-1a显着降低了lin增强病变的中位数,从2.5降至0.3(p≤0.0001)。新的new增强病变的中位数也从2.0降至0.3(p = 0.0002)。血清新蝶呤的诱导方法与以前在白种人RRMS人群中观察到的相似。研究期间未发生新的不良事件。结论:这项针对日本RRMS患者的IMIFNβ-1a的首次研究表明,根据对g增强治疗前和治疗后病变的评估,其疗效水平与白种人患者相似。

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