Efficacy and safety of lemborexant vs placebo in treating adults with insomnia disorder: a systematic review and meta-analysis of 1976 patients

失眠症 荟萃分析 安慰剂 原发性失眠 科克伦图书馆 睡眠起始潜伏期 睡眠开始 随机对照试验 医学 内科学 睡眠障碍 精神科 心理学 物理疗法 替代医学 病理
作者
Mohamed A. Alsaied,Abdelrahman M. Elettreby,Ibrahim Serag,Jaisingh Rajput,Nourhan Abas Zabady,Huansheng Li,Ahmed A. Abo Elnaga
出处
期刊:Naunyn-schmiedebergs Archives of Pharmacology [Springer Science+Business Media]
标识
DOI:10.1007/s00210-025-04072-4
摘要

Abstract 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.
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