Wade Alan G, Ford Ian, Crawford Gordon, McMahon Alex D, Nir Tali, Laudon Moshe, Zisapel Nava
CPS Research, Glasgow, UK.
Curr Med Res Opin. 2007 Oct;23(10):2597-605. doi: 10.1185/030079907X233098.
Melatonin, the hormone produced nocturnally by the pineal gland, serves as a circadian time cue and sleep-anticipating signal in humans. With age, melatonin production declines and the prevalence of sleep disorders, particularly insomnia, increases. The efficacy and safety of a prolonged release melatonin formulation (PR-melatonin; Circadin* 2 mg) were examined in insomnia patients aged 55 years and older.
Randomised, double blind, placebo-controlled.
Primary care.
From 1248 patients pre-screened and 523 attending visit 1, 354 males and females aged 55-80 years were admitted to the study, 177 to active medication and 177 to placebo. The study was conducted by primary care physicians in the West of Scotland and consisted of a 2-week, single blind, placebo run-in period followed by a 3-week double blind treatment period with PR-melatonin or placebo, one tablet per day at 2 hours before bedtime.
Responder rate (concomitant improvement in sleep quality and morning alertness on Leeds Sleep Evaluation Questionnaire [LSEQ]), other LSEQ assessments, Pittsburgh Sleep Quality Index (PSQI) global score, other PSQI assessments, Quality of Night and Quality of Day derived from a diary, Clinical Global Improvement scale (CGI) score and quality of life (WHO-5 well being index).
Of the 354 patients entering the active phase of the study, 20 failed to complete visit 3 (eight PR-melatonin; 12 Placebo). The principal reasons for drop-out were patient decision and lost to follow-up. Significant differences in favour of PR-melatonin vs. placebo treatment were found in concomitant and clinically relevant improvements in quality of sleep and morning alertness, demonstrated by responder analysis (26% vs. 15%; p = 0.014) as well as on each of these parameters separately. A significant and clinically relevant shortening of sleep latency to the same extent as most frequently used sleep medications was also found (-24.3 vs.-12.9 minutes; p = 0.028). Quality of life also improved significantly (p = 0.034).
PR-melatonin results in significant and clinically meaningful improvements in sleep quality, morning alertness, sleep onset latency and quality of life in primary insomnia patients aged 55 years and over.
The trial was conducted prior to registration being introduced.
褪黑素是松果体夜间分泌的一种激素,在人类中作为昼夜节律时间线索和睡眠预期信号。随着年龄增长,褪黑素分泌减少,睡眠障碍尤其是失眠的患病率增加。本研究对55岁及以上失眠患者使用褪黑素缓释制剂(PR-褪黑素;Circadin*2毫克)的疗效和安全性进行了研究。
随机、双盲、安慰剂对照。
初级保健机构。
从1248例预筛查患者和523例参加第1次就诊的患者中,选取354例年龄在55 - 80岁的男性和女性纳入研究,177例接受活性药物治疗,177例接受安慰剂治疗。该研究由苏格兰西部的初级保健医生进行,包括一个为期2周的单盲、安慰剂导入期,随后是一个为期3周的双盲治疗期,使用PR-褪黑素或安慰剂,睡前2小时每天服用一片。
应答率(利兹睡眠评估问卷[LSEQ]中睡眠质量和早晨警觉性同时改善)、其他LSEQ评估、匹兹堡睡眠质量指数(PSQI)总分、其他PSQI评估、日记得出的夜间质量和日间质量、临床总体改善量表(CGI)评分及生活质量(WHO-5幸福指数)。
在进入研究活跃期的354例患者中,20例未完成第3次就诊(8例使用PR-褪黑素;12例使用安慰剂)。退出的主要原因是患者自行决定和失访。应答者分析显示,与安慰剂治疗相比,PR-褪黑素治疗在睡眠质量和早晨警觉性的同时及临床相关改善方面存在显著差异(26%对15%;p = 0.014),且在这些参数中的每一项上均如此。还发现睡眠潜伏期显著且在临床上相关地缩短,程度与最常用的睡眠药物相同(-24.3对-12.9分钟;p = 0.028)。生活质量也有显著改善(p = 0.034)。
PR-褪黑素可使55岁及以上原发性失眠患者的睡眠质量、早晨警觉性、入睡潜伏期和生活质量得到显著且具有临床意义的改善。
该试验在引入注册之前进行。