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金刚烷胺用于治疗帕金森病的运动障碍和运动波动。

Amantadine as treatment for dyskinesias and motor fluctuations in Parkinson's disease.

作者信息

Verhagen Metman L, Del Dotto P, van den Munckhof P, Fang J, Mouradian M M, Chase T N

机构信息

Experimental Therapeutics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892-1406, USA.

出版信息

Neurology. 1998 May;50(5):1323-6. doi: 10.1212/wnl.50.5.1323.

Abstract

OBJECTIVE

To determine the effects of the N-methyl-D-aspartate (NMDA) antagonist amantadine on levodopa-associated dyskinesias and motor fluctuations in Parkinson's disease (PD).

BACKGROUND

NMDA receptor blockade can ameliorate levodopa-induced dyskinesias in primates and PD patients. Amantadine, a well-tolerated and modestly effective antiparkinsonian agent, was recently found to possess NMDA antagonistic properties.

METHODS

Eighteen patients with advanced PD participated in a double-blind, placebo-controlled, cross-over study. At the end of each 3-week treatment arm, parkinsonian and dyskinesia scores were obtained during a steady-state intravenous levodopa infusion. Motor fluctuations and dyskinesias were also documented with patient-kept diaries and Unified Parkinson's Disease Rating Scale (UPDRS) interviews.

RESULTS

In the 14 patients completing this trial, amantadine reduced dyskinesia severity by 60% (p = 0.001) compared to placebo, without altering the antiparkinsonian effect of levodopa. Motor fluctuations occurring with patients' regular oral levodopa regimen also improved according to UPDRS and patient-kept diaries.

CONCLUSIONS

These findings suggest that amantadine given as adjuvant to levodopa can markedly improve motor response complications and support the view that hyperfunction of NMDA receptors contributes to the pathogenesis of levodopa-associated motor complications.

摘要

目的

确定N-甲基-D-天冬氨酸(NMDA)拮抗剂金刚烷胺对帕金森病(PD)中左旋多巴相关异动症和运动波动的影响。

背景

NMDA受体阻断可改善灵长类动物和PD患者中左旋多巴诱发的异动症。金刚烷胺是一种耐受性良好且疗效一般的抗帕金森病药物,最近发现它具有NMDA拮抗特性。

方法

18例晚期PD患者参与了一项双盲、安慰剂对照、交叉研究。在每个为期3周的治疗阶段结束时,在静脉输注左旋多巴达到稳态期间获取帕金森病评分和异动症评分。运动波动和异动症也通过患者的日记记录以及统一帕金森病评定量表(UPDRS)访谈进行记录。

结果

在完成该试验的14例患者中,与安慰剂相比,金刚烷胺使异动症严重程度降低了60%(p = 0.001),且未改变左旋多巴的抗帕金森病作用。根据UPDRS和患者日记记录,患者常规口服左旋多巴治疗方案时出现的运动波动也有所改善。

结论

这些发现表明,作为左旋多巴辅助用药的金刚烷胺可显著改善运动反应并发症,并支持NMDA受体功能亢进促成左旋多巴相关运动并发症发病机制的观点。

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