Wasdell Michael B, Jan James E, Bomben Melissa M, Freeman Roger D, Rietveld Wop J, Tai Joseph, Hamilton Donald, Weiss Margaret D
Melatonin Research Group, Department of Psychiatry, BC Children's Hospital, Vancouver, Canada.
J Pineal Res. 2008 Jan;44(1):57-64. doi: 10.1111/j.1600-079X.2007.00528.x.
The purpose of this study was to determine the efficacy of controlled-release (CR) melatonin in the treatment of delayed sleep phase syndrome and impaired sleep maintenance of children with neurodevelopmental disabilities including autistic spectrum disorders. A randomized double-blind, placebo-controlled crossover trial of CR melatonin (5 mg) followed by a 3-month open-label study was conducted during which the dose was gradually increased until the therapy showed optimal beneficial effects. Sleep characteristics were measured by caregiver who completed somnologs and wrist actigraphs. Clinician rating of severity of the sleep disorder and improvement from baseline, along with caregiver ratings of global functioning and family stress were also obtained. Fifty-one children (age range 2-18 years) who did not respond to sleep hygiene intervention were enrolled. Fifty patients completed the crossover trial and 47 completed the open-label phase. Recordings of total night-time sleep and sleep latency showed significant improvement of approximately 30 min. Similarly, significant improvement was observed in clinician and parent ratings. There was additional improvement in the open-label somnolog measures of sleep efficiency and the longest sleep episode in the open-label phase. Overall, the therapy improved the sleep of 47 children and was effective in reducing family stress. Children with neurodevelopmental disabilities, who had treatment resistant chronic delayed sleep phase syndrome and impaired sleep maintenance, showed improvement in melatonin therapy.
本研究的目的是确定控释褪黑素在治疗包括自闭症谱系障碍在内的神经发育障碍儿童的睡眠时相延迟综合征和睡眠维持障碍方面的疗效。进行了一项随机双盲、安慰剂对照的交叉试验,使用控释褪黑素(5毫克),随后进行为期3个月的开放标签研究,在此期间逐渐增加剂量,直到治疗显示出最佳有益效果。睡眠特征由完成睡眠日志和手腕活动记录仪的照料者进行测量。还获得了临床医生对睡眠障碍严重程度和相对于基线的改善情况的评分,以及照料者对整体功能和家庭压力的评分。招募了51名对睡眠卫生干预无反应的儿童(年龄范围2至18岁)。50名患者完成了交叉试验,47名完成了开放标签阶段。夜间总睡眠时间和睡眠潜伏期的记录显示有显著改善,约为30分钟。同样,临床医生和家长的评分也有显著改善。在开放标签阶段,睡眠效率的睡眠日志测量以及最长睡眠时段方面有进一步改善。总体而言,该疗法改善了47名儿童的睡眠,并有效减轻了家庭压力。患有神经发育障碍、患有治疗抵抗性慢性睡眠时相延迟综合征和睡眠维持障碍的儿童,在褪黑素治疗中显示出改善。