Roth Thomas, Seiden David, Wang-Weigand Sherry, Zhang Jeffrey
Sleep Disorders and Research Center, Detroit, MI 48202, USA.
Curr Med Res Opin. 2007 May;23(5):1005-14. doi: 10.1185/030079907x178874.
To assess the efficacy and safety of ramelteon, a selective melatonin MT1/MT2-receptor agonist, for insomnia treatment in older adults.
In a randomized, 9-week, 3-period crossover trial conducted at 17 sleep centers, older adults (N = 100) with chronic primary insomnia (37 men, 63 women; mean age [range], 70.7 [65-83] years) were administered placebo, ramelteon 4 mg, and ramelteon 8 mg in three treatment phases for two consecutive nights. Each phase was separated by 5- to 12-day washout periods. Sleep was monitored via polysomnography. Subjective sleep parameters, using a Postsleep Questionnaire, were recorded, and residual pharmacologic effects were assessed.
Statistically significant reductions in latency to persistent sleep were observed with both ramelteon 4 mg and 8 mg compared to placebo (28.7 min vs. 38.4 min, p < 0.001; 30.8 min vs. 38.4 min, p = 0.005, respectively). Total sleep time (p = 0.036 and p = 0.007, respectively) and sleep efficiency (p = 0.037 and p = 0.007, respectively) were also significantly improved with ramelteon 4 mg and 8 mg compared to placebo. Statistically significant reductions in subjective sleep latency on a Postsleep Questionnaire were reported with ramelteon 4 mg versus placebo (p = 0.037), but not ramelteon 8 mg (p = 0.120); no significant differences on other subjective sleep assessments were reported. A lack of power limits interpretation of self-reported sleep parameters. Incidences of adverse events considered treatment related were placebo (7%), ramelteon 4 mg (11%), and ramelteon 8 mg (5%). No residual pharmacologic effects were observed via Digit Symbol Substitution Test, memory recall tests (immediate and delayed), visual analog scales (feelings and mood), and Postsleep Questionnaire (level of alertness and ability to concentrate).
In older adults with chronic primary insomnia, ramelteon produced significant reductions in latency to persistent sleep and increases in total sleep time and sleep efficacy, and showed no evidence of adverse next-day psychomotor or cognitive effects.
评估选择性褪黑素MT1/MT2受体激动剂雷美替胺治疗老年人失眠的有效性和安全性。
在17个睡眠中心进行的一项为期9周的随机、3阶段交叉试验中,100名患有慢性原发性失眠的老年人(37名男性,63名女性;平均年龄[范围],70.7[65 - 83]岁)在三个治疗阶段连续两晚分别服用安慰剂、4毫克雷美替胺和8毫克雷美替胺。每个阶段之间有5至12天的洗脱期。通过多导睡眠图监测睡眠情况。使用睡眠后问卷记录主观睡眠参数,并评估残留药理作用。
与安慰剂相比,4毫克和8毫克雷美替胺均使持续睡眠潜伏期出现统计学显著缩短(分别为28.7分钟对38.4分钟,p < 0.001;30.8分钟对38.4分钟,p = 0.005)。与安慰剂相比,4毫克和8毫克雷美替胺还使总睡眠时间(分别为p = 0.036和p = 0.007)和睡眠效率(分别为p = 0.037和p = 0.007)显著提高。在睡眠后问卷上,4毫克雷美替胺与安慰剂相比,主观睡眠潜伏期有统计学显著缩短(p = 0.037),但8毫克雷美替胺无此情况(p = 0.120);在其他主观睡眠评估方面未报告有显著差异。样本量不足限制了对自我报告睡眠参数的解读。被认为与治疗相关的不良事件发生率分别为安慰剂组7%、4毫克雷美替胺组11%和8毫克雷美替胺组5%。通过数字符号替换测试、记忆回忆测试(即时和延迟)、视觉模拟量表(感觉和情绪)以及睡眠后问卷(警觉水平和集中注意力能力)未观察到残留药理作用。
在患有慢性原发性失眠的老年人中,雷美替胺显著缩短了持续睡眠潜伏期,增加了总睡眠时间和睡眠效率,且未显示出次日有不良精神运动或认知影响的证据。