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雷沙吉兰作为左旋多巴辅助治疗对帕金森病关期严重程度的影响。

Effect of rasagiline as adjunct therapy to levodopa on severity of OFF in Parkinson's disease.

机构信息

Institute of Neurology, IRCCS San Raffaele, Pisana, Rome, Italy.

出版信息

Eur J Neurol. 2011 Dec;18(12):1373-8. doi: 10.1111/j.1468-1331.2011.03512.x. Epub 2011 Sep 6.

Abstract

BACKGROUND

The LARGO study demonstrated that rasagiline 1 mg/day as adjunct to levodopa significantly reduces OFF time to the same magnitude as adjunct entacapone. This substudy of LARGO aimed to assess the effect of rasagiline and entacapone on the motor symptoms of PD during the practically defined OFF state.

METHODS

LARGO was a randomized, double-blind, multicenter trial that assessed the efficacy and safety of rasagiline (1 mg/day), entacapone (200 mg with each levodopa dose), and placebo in 687 levodopa-treated PD patients with motor fluctuations. A substudy of LARGO measured UPDRS motor scores in the practically defined OFF state in 32 rasagiline, 36 entacapone, and 37 placebo patients.

RESULTS

Treatment with rasagiline produced a significant improvement over placebo of 5.64 units in UPDRS motor OFF score (P = 0.013 vs. placebo). By contrast, the effect of adjunct entacapone was not significant (P = 0.14 vs. placebo). Whereas rasagiline also showed a trend in reducing the UPDRS-ADL OFF score (P = 0.058 vs. placebo), no such trend was noted for entacapone (P = 0.26 vs. placebo). Retrospective analysis, using the Bonferroni correction, of UPDRS motor subdomains further revealed that rasagiline, but not entacapone, significantly improved bradykinesia (P < 0.001) and showed trends for improvements in facial expression, speech, and axial impairment during OFF time.

CONCLUSIONS

This study provides the first objectively measured evidence that adjunct rasagiline 1 mg/day is effective in reducing the severity of motor symptoms in the OFF state. This suggests a continuous effect of rasagiline 1 mg/day throughout the day and night and is consistent with its extended duration of therapeutic action.

摘要

背景

LARGO 研究表明,雷沙吉兰 1mg/日作为左旋多巴的辅助治疗,可显著减少关期时间,与辅助恩他卡朋的效果相当。LARGO 的这项亚研究旨在评估雷沙吉兰和恩他卡朋对 PD 患者实际定义的关期运动症状的影响。

方法

LARGO 是一项随机、双盲、多中心试验,评估了雷沙吉兰(1mg/日)、恩他卡朋(每剂左旋多巴 200mg)和安慰剂在 687 名左旋多巴治疗的有运动波动的 PD 患者中的疗效和安全性。LARGO 的一项亚研究测量了 32 名雷沙吉兰、36 名恩他卡朋和 37 名安慰剂患者在实际定义的关期状态下 UPDRS 运动评分。

结果

与安慰剂相比,雷沙吉兰治疗显著改善 UPDRS 运动关期评分 5.64 个单位(P = 0.013 与安慰剂)。相比之下,辅助恩他卡朋的效果不显著(P = 0.14 与安慰剂)。虽然雷沙吉兰也显示出降低 UPDRS-ADL 关期评分的趋势(P = 0.058 与安慰剂),但恩他卡朋没有这种趋势(P = 0.26 与安慰剂)。使用 Bonferroni 校正对 UPDRS 运动亚域的回顾性分析进一步表明,雷沙吉兰而非恩他卡朋显著改善了运动迟缓(P < 0.001),并且在关期时面部表情、言语和轴性损害方面也有改善的趋势。

结论

这项研究提供了首次客观测量的证据,表明辅助雷沙吉兰 1mg/日可有效减轻关期运动症状的严重程度。这表明雷沙吉兰 1mg/日在白天和夜间都有持续的作用,与它延长的治疗作用时间一致。

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