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艾司米氮平治疗非老年原发性失眠成年患者:一项为期6周的随机睡眠实验室试验的疗效与安全性

Esmirtazapine in non-elderly adult patients with primary insomnia: efficacy and safety from a randomized, 6-week sleep laboratory trial.

作者信息

Ivgy-May Neely, Ruwe Frank, Krystal Andrew, Roth Thomas

机构信息

Merck & Co., Inc., Kenilworth, NJ, USA.

MSD, Oss, The Netherlands.

出版信息

Sleep Med. 2015 Jul;16(7):838-44. doi: 10.1016/j.sleep.2015.04.001. Epub 2015 Apr 16.

Abstract

OBJECTIVE

Esmirtazapine (Org 50081), a medication that binds with high affinity to serotonin 5-HT2A and histamine-1 receptors, was evaluated as a potential treatment for insomnia.

METHODS

Adults with primary insomnia were treated with esmirtazapine (3.0 or 4.5 mg) or placebo in this 6-week, double-blind, randomized, polysomnography (PSG) study. The end points included wake time after sleep onset (WASO) (primary), latency to persistent sleep, and total sleep time. Patient-reported parameters were also evaluated, including sleep quality and satisfaction with sleep duration. Residual daytime effects and rebound insomnia (sleep parameters during the single-blind placebo run-out week after treatment ended) were also assessed.

RESULTS

Overall, 419 patients were randomized and 366 (87%) completed treatment. The median decrease in PSG WASO (double-blind average) was 20.5 min for placebo, and 52.0 min and 53.6 min for the 3.0- and 4.5-mg esmirtazapine groups, respectively (P < 0.0001 vs. placebo for both doses). Changes in the other PSG parameters and in all patient-reported parameters were also statistically significant with both doses versus placebo. Overall, 35-42% of esmirtazapine-treated patients had adverse events (AEs) versus 29% in the placebo group. AEs were mild or moderate in most esmirtazapine-treated patients. Furthermore, the incidence of AEs leading to discontinuation was low (<8%).

CONCLUSIONS

Six weeks of treatment with esmirtazapine was associated with consistent improvements in objective and patient-reported parameters of sleep onset, maintenance, and duration. It was generally well tolerated, and residual daytime effects were minimal and no rebound insomnia was observed.

摘要

目的

评估依米氮平(Org 50081)作为一种对5-羟色胺5-HT2A和组胺-1受体具有高亲和力的药物治疗失眠的潜力。

方法

在这项为期6周的双盲、随机、多导睡眠图(PSG)研究中,患有原发性失眠的成年人接受依米氮平(3.0或4.5毫克)或安慰剂治疗。终点指标包括入睡后清醒时间(WASO)(主要指标)、持续睡眠潜伏期和总睡眠时间。还评估了患者报告的参数,包括睡眠质量和对睡眠时间的满意度。还评估了残余日间效应和反弹性失眠(治疗结束后单盲安慰剂停药周期间的睡眠参数)。

结果

总体而言,419名患者被随机分组,366名(87%)完成治疗。安慰剂组PSG的WASO中位数下降(双盲平均值)为20.5分钟,3.0毫克和4.5毫克依米氮平组分别为52.0分钟和53.6分钟(两种剂量与安慰剂相比,P均<0.0001)。两种剂量与安慰剂相比,其他PSG参数和所有患者报告参数的变化也具有统计学意义。总体而言,依米氮平治疗的患者中有35%-42%发生不良事件(AE),而安慰剂组为29%。大多数接受依米氮平治疗的患者的AE为轻度或中度。此外,导致停药的AE发生率较低(<8%)。

结论

依米氮平治疗6周与入睡、维持睡眠和睡眠时间的客观指标及患者报告指标的持续改善相关。其耐受性总体良好,残余日间效应极小,未观察到反弹性失眠。

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