Department of Neurology, Kyung Hee University Hospital, Seoul, Republic of Korea.
Department of Neurology, Seoul Central Clinic, Seoul, Republic of Korea.
J Neurol Sci. 2019 Jun 15;401:81-86. doi: 10.1016/j.jns.2019.04.029. Epub 2019 Apr 23.
Clonazepam is considered to be a first-line treatment for rapid eye movement sleep-related behavior disorder (RBD) in Parkinson's disease (PD). The purpose of this study was to determine the short-term efficacy and safety of clonazepam for the treatment of probable RBD (pRBD) in patients with PD.
We conducted a four-week, randomized, double-blind, placebo-controlled trial of clonazepam (0.5 mg/day at bedtime) compared to a placebo for RBD symptoms in patients with PD. Patients aged 30 years or older who had a caregiver that could observe RBD symptoms were recruited between April 2015 and February 2016. The primary outcome was the Clinical Global Impressions-Improvement (CGII) score at week four, and we compared scores between the clonazepam and placebo groups.
A total of 40 patients were enrolled, with 20 assigned to receive clonazepam and 20 to receive the placebo. The CGI-I score at four weeks indicated an improvement in RBD symptoms in both the clonazepam (median score [minimum, maximum] = 2 [1,5]) and placebo (3 [1,6]) groups, with no significant difference between the groups (p = .253). The secondary outcomes were not significantly different between the clonazepam and placebo groups.
Both clonazepam and placebo tended toward improvement on pRBD symptoms in patients with PD. No firm conclusion on efficacy of clonazepam was drawn due to limitations in the study design. This study emphasized the importance of conducting future large-scale, randomized trials with better assessment tools and polysomnography to provide evidence for the benefit of clonazepam.
氯硝西泮被认为是治疗帕金森病(PD)快动眼睡眠相关行为障碍(RBD)的一线药物。本研究旨在确定氯硝西泮治疗 PD 患者可能的 RBD(pRBD)的短期疗效和安全性。
我们进行了为期四周、随机、双盲、安慰剂对照试验,比较氯硝西泮(睡前 0.5mg/天)与安慰剂治疗 PD 患者的 RBD 症状。2015 年 4 月至 2016 年 2 月期间,招募了年龄在 30 岁及以上且有可以观察 RBD 症状的照顾者的患者。主要结局是第 4 周的临床总体印象改善(CGII)评分,我们比较了氯硝西泮组和安慰剂组的评分。
共纳入 40 例患者,其中 20 例接受氯硝西泮治疗,20 例接受安慰剂治疗。四周时的 CGI-I 评分表明,氯硝西泮组(中位数[最小,最大]为 2[1,5])和安慰剂组(3[1,6])的 RBD 症状均有所改善,两组间无显著差异(p=0.253)。次要结局在氯硝西泮组和安慰剂组之间也无显著差异。
氯硝西泮和安慰剂均倾向于改善 PD 患者的 pRBD 症状。由于研究设计的限制,未能得出氯硝西泮疗效的确切结论。本研究强调了进行未来使用更好评估工具和多导睡眠图的大规模、随机试验的重要性,以提供氯硝西泮有益的证据。