Rosenberg Russell, Seiden David J, Hull Steven G, Erman Milton, Schwartz Howard, Anderson Christen, Prosser Warren, Shanahan William, Sanchez Matilde, Chuang Emil, Roth Thomas
NeuroTrials Research and Atlanta School of Sleep Medicine, Atlanta 30342, USA.
Sleep. 2008 Dec;31(12):1663-71. doi: 10.1093/sleep/31.12.1663.
Insomnia is a condition affecting 10% to 15% of the adult population and is characterized by difficulty falling asleep, difficulty staying asleep, or nonrestorative sleep, accompanied by daytime impairment or distress. This study evaluates APD125, a selective inverse agonist of the 5-HT(2A) receptor, for treatment of chronic insomnia, with particular emphasis on sleep maintenance. In phase 1 studies, APD125 improved sleep maintenance and was well tolerated.
Adult subjects (n=173) with DSM-IV defined primary insomnia were randomized into a multicenter, double-blind, placebo-controlled, 3-way crossover study to compare 2 doses of APD125 (10 mg and 40 mg) with placebo. Each treatment period was 7 days with a 7- to 9-day washout period between treatments. Polysomnographic recordings were performed at the initial 2 screening nights and at nights (N) 1/2 and N 6/7 of each treatment period.
APD125 was associated with significant improvements in key sleep maintenance parameters measured by PSG. Wake time after sleep onset decreased (SEM) by 52.5 (3.2) min (10 mg) and 53.5 (3.5) min (40 mg) from baseline to N 1/2 vs. 37.8 (3.4) min for placebo, (P < 0.0001 for both doses vs. placebo), and by 51.7 (3.4) min (P = 0.01) and 48.0 (3.6) min (P = 0.2) at N 6/7 vs. 44.0 (3.8) min for placebo. Significant APD125 effects on wake time during sleep were also seen (P < 0.0001 N 1/2, P < 0.001 N 6/7). The number of arousals and number of awakenings decreased significantly with APD125 treatment compared to placebo. Slow wave sleep showed a statistically significant dose-dependent increase. There was no significant decrease in latency to persistent sleep. No serious adverse events were reported, and no meaningful differences in adverse event profiles were observed between either dose of APD125 and placebo. APD125 was not associated with next-day psychomotor impairment as measured by Digit Span, Digit Symbol Copy, and Digit Symbol Coding Tests.
APD125 produced statistically significant improvements in objective parameters of sleep maintenance and sleep consolidation and was well tolerated in adults with primary chronic insomnia.
失眠是一种影响10%至15%成年人口的病症,其特征为入睡困难、难以维持睡眠或睡眠质量不佳,并伴有日间功能障碍或困扰。本研究评估了5-HT(2A)受体选择性反向激动剂APD125治疗慢性失眠的效果,尤其着重于睡眠维持方面。在1期研究中,APD125改善了睡眠维持情况,且耐受性良好。
将符合DSM-IV定义的原发性失眠成年受试者(n = 173)随机分组,进行一项多中心、双盲、安慰剂对照的三向交叉研究,以比较2种剂量的APD125(10毫克和40毫克)与安慰剂。每个治疗期为7天,治疗之间有7至9天的洗脱期。在最初的2个筛查夜以及每个治疗期的第1/2夜和第6/7夜进行多导睡眠图记录。
APD125与通过多导睡眠图测量的关键睡眠维持参数的显著改善相关。从基线到第1/2夜,入睡后觉醒时间(标准误)在10毫克剂量组减少了52.5(3.2)分钟,40毫克剂量组减少了53.5(3.5)分钟,而安慰剂组减少了37.8(3.4)分钟(两种剂量组与安慰剂组相比,P均<0.0001);在第6/7夜,10毫克剂量组减少了51.7(3.4)分钟(P = 0.01),40毫克剂量组减少了48.0(3.6)分钟(P = 0.2),而安慰剂组减少了44.0(3.8)分钟。APD125对睡眠期间觉醒时间也有显著影响(第1/2夜P < 0.0001,第6/7夜P < 0.001)。与安慰剂相比,APD125治疗使觉醒次数和醒来次数显著减少。慢波睡眠呈现出统计学上显著的剂量依赖性增加。持续睡眠潜伏期没有显著缩短。未报告严重不良事件,且在两种剂量的APD125与安慰剂之间,不良事件谱未观察到有意义的差异。通过数字广度、数字符号复制和数字符号编码测试测量,APD125与次日精神运动功能损害无关。
APD125在睡眠维持和睡眠巩固的客观参数方面产生了统计学上显著的改善,并且在患有原发性慢性失眠的成年人中耐受性良好。