Dowling Glenna A, Mastick Judith, Colling Eric, Carter Julie H, Singer Clifford M, Aminoff Michael J
Institute on Aging Research Center, 3330 Geary Blvd., San Francisco, CA, USA.
Sleep Med. 2005 Sep;6(5):459-66. doi: 10.1016/j.sleep.2005.04.004.
Many patients with Parkinson's disease (PD) experience sleep-related symptoms. Studies in other populations indicate that melatonin can increase sleep efficiency, decrease nighttime activity, and shorten sleep latency, but there has been little research on the use of melatonin in PD. The purpose of this study was to compare the effects of two doses of melatonin to placebo on sleep, daytime sleepiness, and level of function in patients with PD who complained of sleep disturbances.
A multi-site double-blind placebo-controlled cross-over trial was employed; 40 subjects completed the 10-week protocol. There was a 2-week screening period, 2-week treatment periods, and 1-week washouts between treatments. Nocturnal sleep was assessed by actigraphy and diaries, whereas daytime sleepiness and function were assessed by the Epworth Sleepiness Scale (ESS), Stanford Sleepiness Scale (SSS), and General Sleep Disturbance Scale (GSDS).
Repeated measures analysis of variance revealed a significant improvement in total nighttime sleep time during the 50 mg melatonin treatment compared to placebo. There was significant improvement in subjective sleep disturbance, sleep quantity, and daytime sleepiness during the 5 mg melatonin treatment compared to placebo as assessed by the GSDS.
Although we found a statistically significant improvement in actigraphically measured total sleep time on 50 mg melatonin compared to 5 mg or placebo, this small improvement (10 min) may not be clinically significant. However, the significant improvement found in subjective sleep disturbance suggests that these modest effects may be clinically relevant in this patient population.
许多帕金森病(PD)患者存在与睡眠相关的症状。对其他人群的研究表明,褪黑素可提高睡眠效率、减少夜间活动并缩短睡眠潜伏期,但关于褪黑素在帕金森病中的应用研究较少。本研究的目的是比较两种剂量的褪黑素与安慰剂对主诉睡眠障碍的帕金森病患者的睡眠、日间嗜睡及功能水平的影响。
采用多中心双盲安慰剂对照交叉试验;40名受试者完成了为期10周的方案。有2周的筛查期、2周的治疗期以及治疗期间1周的洗脱期。通过活动记录仪和日记评估夜间睡眠,而通过爱泼华嗜睡量表(ESS)、斯坦福嗜睡量表(SSS)和一般睡眠障碍量表(GSDS)评估日间嗜睡和功能。
重复测量方差分析显示,与安慰剂相比,50毫克褪黑素治疗期间总夜间睡眠时间有显著改善。根据GSDS评估,与安慰剂相比,5毫克褪黑素治疗期间主观睡眠障碍、睡眠质量和日间嗜睡有显著改善。
尽管我们发现与5毫克或安慰剂相比,50毫克褪黑素在活动记录仪测量的总睡眠时间上有统计学显著改善,但这种微小改善(10分钟)可能不具有临床意义。然而,主观睡眠障碍方面的显著改善表明,这些适度的效果在该患者群体中可能具有临床相关性。