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用甲基苯丙胺治疗发作性睡病。

Treatment of narcolepsy with methamphetamine.

作者信息

Mitler M M, Hajdukovic R, Erman M K

机构信息

Sleep Disorders Center, Scripps Clinic and Research Foundation, La Jolla, California 92037.

出版信息

Sleep. 1993 Jun;16(4):306-17.

Abstract

Eight pairs of subjects (each consisting of a narcoleptic and a control matched on the basis of age, sex, educational background and job) were evaluated under the following double-blind, randomized treatment conditions: baseline, placebo, low dose and high dose methamphetamine. Subjects were drug-free for 2 weeks prior to beginning the protocol. Methamphetamine was the only drug taken during the protocol and was given in a single morning dose of 0, 20 or 40-60 mg to narcoleptics and 0, 5 or 10 mg to controls. The protocol was 28 days long, with each of the four treatment conditions lasting 4 days followed by 3 days of washout. Nighttime polysomnography and daytime testing were done during the last 24 hours of each treatment condition. Daytime sleep tendency was assessed with the multiple sleep latency test (MSLT). Daytime performance was assessed with performance tests including a simple, computer-based driving task. Narcoleptics' mean MSLT sleep latency increased from 4.3 minutes on placebo to 9.3 minutes on high dose, compared with an increase from 10.4 to 17.1 minutes for controls. Narcoleptics' error rate on the driving task decreased from 2.53% on placebo to 0.33% on high dose, compared with a decrease from 0.22% to 0.16% for controls. The effects of methamphetamine on nocturnal sleep were generally dose-dependent and affected sleep continuity and rapid eye movement (REM) sleep. Elimination half life was estimated to be between 15.9 and 22.0 hours. Mild side effects emerged in a dose-dependent fashion and most often involved the central nervous system and gastrointestinal tract. We concluded that methamphetamine caused a dose-dependent decrease in daytime sleep tendency and improvement in performance in both narcoleptics and controls. Methamphetamine at doses of 40-60 mg allowed narcoleptics to function at levels comparable to those of unmedicated controls.

摘要

八对受试者(每对由一名发作性睡病患者和一名在年龄、性别、教育背景和工作方面相匹配的对照者组成)在以下双盲、随机治疗条件下进行了评估:基线期、安慰剂期、低剂量和高剂量甲基苯丙胺期。在开始该方案前,受试者已停药两周。甲基苯丙胺是方案期间服用的唯一药物,发作性睡病患者在早晨单次服用剂量为0、20或40 - 60毫克,对照者为0、5或10毫克。该方案为期28天,四个治疗阶段各持续4天,随后是3天的洗脱期。在每个治疗阶段的最后24小时进行夜间多导睡眠图监测和白天测试。白天睡眠倾向通过多次睡眠潜伏期测试(MSLT)进行评估。白天表现通过包括基于计算机的简单驾驶任务在内的表现测试进行评估。发作性睡病患者的平均MSLT睡眠潜伏期从安慰剂期的4.3分钟增加到高剂量期的9.3分钟,而对照者从10.4分钟增加到17.1分钟。发作性睡病患者在驾驶任务中的错误率从安慰剂期的2.53%降至高剂量期的0.33%,对照者从0.22%降至0.16%。甲基苯丙胺对夜间睡眠的影响通常呈剂量依赖性,影响睡眠连续性和快速眼动(REM)睡眠。消除半衰期估计在15.9至22.0小时之间。轻度副作用呈剂量依赖性出现,最常累及中枢神经系统和胃肠道。我们得出结论,甲基苯丙胺导致发作性睡病患者和对照者白天睡眠倾向呈剂量依赖性降低,表现得到改善。40 - 60毫克剂量的甲基苯丙胺使发作性睡病患者的功能水平与未用药的对照者相当。

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