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金刚烷胺治疗帕金森病的长期抗运动障碍疗效。

Long-term antidyskinetic efficacy of amantadine in Parkinson's disease.

机构信息

Department of Neurology, Medical University Innsbruck, Innsbruck, Austria.

出版信息

Mov Disord. 2010 Jul 30;25(10):1357-63. doi: 10.1002/mds.23034.

DOI:10.1002/mds.23034
PMID:20198649
Abstract

Several randomized placebo-controlled trials have consistently shown antidyskinetic effects of amantadine in levodopa treated patients with advanced Parkinson's disease (PD). However, all of these were of short duration and there have been claims that the effect of amantadine on levodopa induced dyskinesias (LID's) wear off after about 9 months of treatment. This randomized placebo-controlled parallel-group study was performed to assess the long-term antidyskinetic effect of amantadine in 32 PD patients, who after having been on stable amantadine therapy for LID over at least one year- were switched in a double blind manner to amantadine or placebo and followed for 3 weeks. Dyskinesia duration and intensity were assessed by UPDRS IV items 32 and 33 as well as by patient's diaries. The primary outcome was the score change of UPDRS IV items 32 + 33 between baseline and 3 weeks after treatment as well as the between treatment group comparison of the score change of UPDRS IV items 32 + 33. There was a significant increase of UPDRS IV items 32 + 33 in patients treated with placebo from 3.06 (95% CI, 2.1-4.03) at baseline to 4.28 (95% CI, 3.1-5.4) at three-week follow-up (P = 0.02) compared with no significant change between baseline 3.2 (95% CI, 2.1-4.4) to follow-up 3.6 (95% CI, 2.3-4.8) in patients staying on amantadine. These findings argue for long-term antidyskinetic efficacy of amantadine in PD patients with LID's.

摘要

几项随机安慰剂对照试验一致表明,金刚烷胺对左旋多巴治疗的晚期帕金森病(PD)患者的运动障碍有拮抗作用。然而,所有这些试验的持续时间都很短,并且有人声称,金刚烷胺对左旋多巴诱导的运动障碍(LID)的作用在治疗 9 个月后就会消失。这项随机安慰剂对照平行组研究旨在评估金刚烷胺对 32 名 PD 患者的长期抗运动障碍作用,这些患者在 LID 接受稳定的金刚烷胺治疗至少一年后,以双盲方式切换为金刚烷胺或安慰剂,并随访 3 周。运动障碍的持续时间和强度通过 UPDRS IV 项目 32 和 33 以及患者日记进行评估。主要结局是治疗前与治疗后 3 周 UPDRS IV 项目 32 + 33 的评分变化,以及治疗后 UPDRS IV 项目 32 + 33 的评分变化的治疗组间比较。与继续接受金刚烷胺治疗的患者相比,接受安慰剂治疗的患者的 UPDRS IV 项目 32 + 33 评分从基线时的 3.06(95%CI,2.1-4.03)显著增加到治疗后 3 周时的 4.28(95%CI,3.1-5.4)(P = 0.02),而继续接受金刚烷胺治疗的患者的评分从基线时的 3.2(95%CI,2.1-4.4)到治疗后 3 周时的 3.6(95%CI,2.3-4.8)没有显著变化。这些发现表明,金刚烷胺对 LID 的 PD 患者具有长期的抗运动障碍作用。

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