Högl B, Saletu M, Brandauer E, Glatzl S, Frauscher B, Seppi K, Ulmer H, Wenning G, Poewe W
Department of Neurology, University of Innsbruck, Austria.
Sleep. 2002 Dec;25(8):905-9.
To assess the therapeutic efficacy of modafinil in the treatment of increased daytime sleepiness in patients with Parkinson's disease (PD).
Double-blind, randomized, placebo-controlled crossover study with two 2-week treatment blocks, separated by a 2-week washout phase.
Tertiary Parkinson's disease care center and sleep laboratory at university hospital neurology department.
Fifteen patients with idiopathic PD and daytime sleepiness (Epworth sleepiness score (ESS) 10 or more).
Administration of placebo or modafinil as a single morning dose in a randomized crossover order. The modafinil dose was 100 mg in the first, and 200 mg in the second treatment week.
At baseline and at the end of each treatment block, sleepiness was evaluated using subjective (perceived sleepiness with the ESS) and objective measures (maintenance of wakefulness test). Twelve patients completed the study (9 male, 3 female; mean age 65.0 +/- 7.6 years, mean disease duration 6.8 +/- 4.1 years). Epworth scores were significantly improved with modafinil (3.42 +/- 3.90) compared to placebo (0.83 +/- 1.99; p = 0.011). Latency to sleep in the maintenance of wakefulness test was not significantly altered by modafinil treatment: 10.9 (3-40)/15.1 (2.5-40) minutes before/after placebo and 12 (2.6-40)/17.8 (4.2-40) minutes before/after modafinil (p = 0.139) [data given as mean +/- standard deviation or median (range)].
The results of this study suggest that modafinil improves daytime sleepiness in PD patients, at least on a subjective or behavioral level. Modafinil treatment may be considered for EDS in PD patients, in whom otherwise treatable causes of Excessive Daytime Sleepiness (EDS) are absent.
评估莫达非尼治疗帕金森病(PD)患者日间嗜睡增加的疗效。
双盲、随机、安慰剂对照交叉研究,有两个为期2周的治疗阶段,中间间隔2周的洗脱期。
大学医院神经科的三级帕金森病护理中心和睡眠实验室。
15例特发性PD且有日间嗜睡症状的患者(爱泼沃斯嗜睡量表评分(ESS)为10分或更高)。
按随机交叉顺序,早晨单次服用安慰剂或莫达非尼。莫达非尼剂量在第一个治疗周为100毫克,第二个治疗周为200毫克。
在基线期和每个治疗阶段结束时,使用主观指标(用ESS评估的嗜睡感)和客观指标(清醒维持试验)评估嗜睡情况。12例患者完成了研究(9例男性,3例女性;平均年龄65.0±7.6岁,平均病程6.8±4.1年)。与安慰剂(0.83±1.99;p = 0.011)相比,莫达非尼治疗后ESS评分显著改善(3.42±3.90)。清醒维持试验中的入睡潜伏期未因莫达非尼治疗而显著改变:安慰剂治疗前后分别为10.9(3 - 40)/15.1(2.5 - 40)分钟,莫达非尼治疗前后分别为12(2.6 - 40)/17.8(4.2 - 40)分钟(p = 0.139)[数据以平均值±标准差或中位数(范围)表示]。
本研究结果表明,莫达非尼可改善PD患者的日间嗜睡,至少在主观或行为层面上如此。对于不存在其他可治疗的日间过度嗜睡(EDS)原因的PD患者的EDS,可考虑使用莫达非尼治疗。