Alsaied Mohamed A, Elettreby Abdelrahman M, Serag Ibrahim, Rajput Jaisingh, Zabady Nourhan Abas, Li Huansheng, Abo Elnaga Ahmed A
Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Department of Family Medicine, Baptist Family Medicine Residency Program, Vaughn Clinic, Montgomery, AL, USA.
Naunyn Schmiedebergs Arch Pharmacol. 2025 Apr 17. doi: 10.1007/s00210-025-04072-4.
Insomnia is a typical sleep disorder in which an individual finds it difficult to fall asleep and stay asleep resulting in poor daytime functioning and decreased health and quality of life. The orexin system, which regulates wakefulness and arousal, is often overactive in individuals with insomnia, disrupting normal sleep patterns. Lemborexant, a dual orexin receptor antagonist, works through the inhibition of the orexin system, thus facilitating increased sleep onset and maintenance of sleep. This systematic review and meta-analysis seek to determine the effectiveness and safety of lemborexant in the treatment of insomnia. A comprehensive search was conducted on PubMed, Scopus, Web of Science, and Cochrane Library, from inception to September 2024. Four randomized controlled trials (RCTs) assessing the efficacy and safety of lemborexant for patients with confirmed DSM-5 diagnosis of insomnia as compared to placebo were included. By adopting a random-effect inverse variance model, RevMan was used to pool dichotomous and continuous data. We employed the ROB2 methodology to evaluate the quality of the evidence, so ensuring the reliability of the findings obtained throughout these investigations. Four studies with a total of 1976 patients were included. Lemborexant was superior to placebo in decreasing sleep onset latency and wake after sleep onset: (MD = - 9.23 min, P = 0.02 and MD = - 19.9 min, P < 0.0001) with 5 mg and (MD = - 12.56 min, P = 0.004) and (MD = - 22.24 min, P < 0.0001) with 10 mg, respectively. In addition, sleep efficiency was statistically significantly higher in the lemborexant group (MD = 6.08%, P < 0.0001) and (MD = 7.46%, P < 0.0001) with 5 mg and 10 mg, respectively. Regarding safety analysis, Treatment emerged adverse events (TEAEs) and somnolence were statistically significantly higher in the lemborexant group (RR = 1.94, P < 0.0001) and (RR = 4.95, P < 0.0001), respectively. In accordance with this systematic review and meta-analysis, lemborexant is an effective pharmacotherapy for the treatment of insomnia as it improves sleep onset latency, wake after sleep onset, and sleep efficiency. Both formulations of 5-mg and 10-mg doses were well tolerated with no significant difference in their effect; however, somnolence was more common relative to placebo. Lemborexant appears to fill a therapeutic gap in the treatment of insomnia but should be used with caution and smaller dose (5 mg) in those who are at risk of developing an excessive daytime somnolence state.
失眠是一种典型的睡眠障碍,患者难以入睡且难以维持睡眠,导致白天功能不佳,健康状况和生活质量下降。调节清醒和觉醒的食欲素系统在失眠患者中通常过度活跃,扰乱了正常的睡眠模式。双食欲素受体拮抗剂lemborexant通过抑制食欲素系统发挥作用,从而促进入睡并维持睡眠。本系统评价和荟萃分析旨在确定lemborexant治疗失眠的有效性和安全性。对PubMed、Scopus、Web of Science和Cochrane图书馆进行了全面检索,检索时间从建库至2024年9月。纳入了四项随机对照试验(RCT),评估lemborexant与安慰剂相比对确诊为DSM-5失眠的患者的疗效和安全性。采用随机效应逆方差模型,使用RevMan汇总二分法和连续数据。我们采用ROB2方法评估证据质量,以确保在这些研究中获得的结果的可靠性。纳入了四项研究,共1976例患者。Lemborexant在缩短入睡潜伏期和减少睡眠中觉醒方面优于安慰剂:5毫克剂量时(MD = -9.23分钟,P = 0.02;MD = -19.9分钟,P < 0.0001),10毫克剂量时(MD = -12.56分钟,P = 0.004;MD = -22.24分钟,P < 0.0001)。此外,lemborexant组的睡眠效率在统计学上显著更高,5毫克和10毫克剂量时分别为(MD = 6.08%,P < 0.0001)和(MD = 7.46%,P < 0.0001)。关于安全性分析,治疗中出现的不良事件(TEAE)和嗜睡在lemborexant组中在统计学上显著更高,分别为(RR = 1.94,P < 0.0001)和(RR = 4.95,P < 0.0001)。根据本系统评价和荟萃分析,lemborexant是治疗失眠的有效药物疗法,因为它可改善入睡潜伏期、睡眠中觉醒和睡眠效率。5毫克和10毫克剂量的两种制剂耐受性良好,效果无显著差异;然而,与安慰剂相比,嗜睡更为常见。Lemborexant似乎填补了失眠治疗的治疗空白,但对于有白天过度嗜睡风险的患者应谨慎使用并采用较小剂量(5毫克)。