治疗失眠症的 Daridorexant。

IF 2 Q3 PSYCHOLOGY, CLINICAL
Health Psychology Research Pub Date : 2022-08-30 eCollection Date: 2022-01-01 DOI:10.52965/001c.37400
Christopher L Robinson, Rajesh Supra, Evan Downs, Saurabh Kataria, Katelyn Parker, Alan D Kaye, Omar Viswanath, Ivan Urits
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引用次数: 0

摘要

审查目的:失眠是一种复杂的睡眠障碍,影响着全世界许多人的生活。失眠症通常伴有并发症,因此是一种需要多因素治疗的复杂疾病。一线疗法是失眠认知行为疗法(CBT-I)。失眠症的药物疗法根据作用机制可分为四类:苯二氮卓受体激动剂(BZRAs)、组胺受体拮抗剂、褪黑素受体激动剂和双奥曲肽受体拮抗剂(DORAs):Daridorexant 是一种双重奥曲肽 1 型和 2 型(OX1 和 OX2)受体拮抗剂,最近获得美国 FDA 批准用于治疗成人失眠症。研究表明,它能有效减轻失眠症状,提高日间功能,改善整体睡眠质量。Daridorexant可缓解患者的失眠症状,同时避免苯二氮卓类药物和镇静剂等传统疗法的严重副作用和依赖性问题。摘要:本文回顾了失眠治疗的最新数据,总结了Daridorexant治疗失眠的安全性和有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Daridorexant for the Treatment of Insomnia.

Purpose of review: Insomnia is a complex sleeping disorder that affects the lives of many individuals worldwide. Insomnia often occurs in the presence of coexisting comorbidities making it a complex disorder that requires a multifactorial approach to therapy. First-line therapy is cognitive-behavioral therapy for insomnia (CBT-I). Pharmacotherapy for insomnia falls into four classes based on mechanism of action: benzodiazepine receptor agonists (BZRAs), histamine receptor antagonists, melatonin receptor agonists, and dual orexin receptor antagonists (DORAs).

Recent findings: Daridorexant is a dual orexin type 1 and types 2 (OX1 and OX2) receptor antagonist that was recently approved by the US FDA for the treatment of adults suffering from insomnia. It was shown to be effective in reducing insomnia symptoms, increasing daytime functioning, and improving the overall quality of sleep. Daridorexant offers patients relief from insomnia while avoiding the severe side effects and dependency issues of traditional treatments like benzodiazepines and sedatives.

Summary: In this article, we review the most recent data on insomnia treatments and summarize the safety and efficacy of daridorexant in treating insomnia.

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来源期刊
Health Psychology Research
Health Psychology Research PSYCHOLOGY, CLINICAL-
CiteScore
2.90
自引率
0.00%
发文量
63
审稿时长
15 weeks
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