Department of Geriatric Neurology, Chinese PLA General Hospital, Beijing, China.
Int J Clin Pract. 2012 Sep;66(9):867-73. doi: 10.1111/j.1742-1241.2012.02987.x.
As a melatonin receptor agonist, ramelteon has been approved in the United States as a treatment for insomnia. As a potential alternation, ramelteon should be further evaluated in different doses and populations. This systematic review with meta-analysis aims to determine the efficacy and safety of ramelteon in the treatment of chronic insomnia.
We systematically searched and identified in Medline, Embase, PsycINFO and Cochrane Library until September 2011. We only included randomised controlled trials focused on ramelteon, vs. placebo, or any other treatment for patients with chronic insomnia. Data were extracted and evaluated by two independent investigators. If neither clinical nor statistical heterogeneity was found, we pooled results using a fixed-effect model.
Eight studies were selected to include from 175 identified references. There were significant improvements in all the outcomes (subjective and polysomnographic sleep latency, total sleep time and latency to REM), except for the percentage of REM. By subgroup analysis, subjective sleep latency was reduced only in the patients of 18-64 years old, without in the patients over 65 years old. For the safety, ramelteon was not associated with higher risk ratio of any frequent adverse events comparing with control.
The efficacy and safety of ramelteon are promising for the chronic insomnia patients. More researches are required for robust conclusions, particularly well-designed; double-blind randomised controlled trials with higher doses of ramelteon (32 or 64 mg) for the older population comparing with other sedative hypnotics.
雷美替胺作为褪黑素受体激动剂,已获美国批准用于治疗失眠症。作为一种潜在的替代药物,雷美替胺应在不同剂量和人群中进一步评估。本系统评价和荟萃分析旨在确定雷美替胺治疗慢性失眠症的疗效和安全性。
我们系统地检索了 Medline、Embase、PsycINFO 和 Cochrane Library,检索时间截至 2011 年 9 月。我们仅纳入了聚焦于雷美替胺的随机对照试验,与安慰剂或任何其他治疗慢性失眠症患者的药物进行比较。由两名独立的研究者提取和评价数据。如果既没有临床异质性也没有统计学异质性,我们将使用固定效应模型对结果进行合并。
从 175 篇已识别的参考文献中选择了 8 项研究纳入。除 REM 百分比外,所有结局(主观和多导睡眠潜伏期、总睡眠时间和 REM 潜伏期)均有显著改善。通过亚组分析,只有 18-64 岁的患者主观睡眠潜伏期缩短,65 岁以上的患者则没有。对于安全性,与对照组相比,雷美替胺并没有增加任何常见不良事件的风险比。
雷美替胺对慢性失眠症患者的疗效和安全性有一定前景。需要更多的研究来得出可靠的结论,特别是对于老年人,需要设计更好的、双盲、随机对照试验,使用更高剂量(32 或 64mg)的雷美替胺与其他镇静催眠药进行比较。