Department of Neurology, Kyung Hee University Hospital at Gangdong, 892 Dongnam-ro, Gangdong-gu, Seoul, 134-727, Republic of Korea.
Department of Medicine, Graduate School, Kyung Hee University, Seoul, Republic of Korea.
Sleep Breath. 2023 Mar;27(1):309-318. doi: 10.1007/s11325-022-02572-8. Epub 2022 Feb 9.
Clonazepam and melatonin are recommended as first-line treatments for isolated rapid eye movement (REM) sleep behavior disorder (iRBD). This study aimed to compare their efficacy and safety in REM sleep without atonia (RWA) and RBD-related symptoms.
This prospective, open-label, randomized trial included patients with video-polysomnography-confirmed iRBD. The patients were randomly assigned to receive either clonazepam 0.5 mg or prolonged-release (PR) melatonin 2 mg 30 min before bedtime for 4 weeks. The primary outcome was changes in RWA on follow-up polysomnography (PSG). Secondary endpoints were changes in other PSG parameters, clinical global improvement-impression scale (CGI-I) scores, and sleep questionnaire scores. The safety endpoint was adverse events.
Of 40 patients with probable RBD considered, 34 were enrolled in the study and randomized. Visual scoring parameters of RWA indices were reduced, and automatic scoring parameters tended to be improved after clonazepam treatment but not after PR melatonin treatment. The proportion of N2 sleep was increased, and N3 and REM sleep were decreased only in the clonazepam group. The clonazepam group tended to answer "much or very much improvement" on the CGI-I more frequently than the PR melatonin group (p = 0.068). Daytime sleepiness and insomnia symptoms were reduced after PR melatonin but not after clonazepam. Depressive symptoms increased after clonazepam. Four of the patients (13.3%) reported mild to moderate adverse events, which were similar between the two groups.
Four weeks of clonazepam, but not PR melatonin, improved RWA. RBD symptom improvement tended to be better after clonazepam than PR melatonin in exchange for increased depressive symptoms and daytime sleepiness.
gov identifier: NCT03255642 (first submitted August 21, 2017).
氯硝西泮和褪黑素被推荐为孤立性快速眼动(REM)睡眠行为障碍(iRBD)的一线治疗药物。本研究旨在比较这两种药物在 REM 睡眠无动(RWA)和 RBD 相关症状方面的疗效和安全性。
这是一项前瞻性、开放标签、随机试验,纳入了经视频多导睡眠图(PSG)证实的 iRBD 患者。患者被随机分配接受氯硝西泮 0.5mg 或延长释放(PR)褪黑素 2mg,在睡前 30 分钟服用,持续 4 周。主要结局是随访 PSG 中 RWA 的变化。次要结局是其他 PSG 参数、临床总体改善印象量表(CGI-I)评分和睡眠问卷评分的变化。安全性终点是不良事件。
在考虑的 40 例可能的 RBD 患者中,34 例被纳入研究并随机分组。氯硝西泮治疗后 RWA 指数的视觉评分参数降低,自动评分参数有改善趋势,但 PR 褪黑素治疗后无改善。N2 睡眠比例增加,N3 和 REM 睡眠仅在氯硝西泮组减少。氯硝西泮组在 CGI-I 上更倾向于回答“明显或非常明显改善”(p=0.068)。PR 褪黑素治疗后白天嗜睡和失眠症状减轻,但氯硝西泮治疗后无改善。氯硝西泮治疗后抑郁症状加重。4 例患者(13.3%)报告有轻度至中度不良事件,两组间相似。
4 周的氯硝西泮治疗而非 PR 褪黑素治疗可改善 RWA。与增加的抑郁症状和白天嗜睡相比,RBD 症状改善在氯硝西泮治疗后比 PR 褪黑素治疗后更倾向于更好。
gov 标识符:NCT03255642(首次提交于 2017 年 8 月 21 日)。