Webber Heather, Badawi Jessica, Calvillo Douglas, Yoon Jin, Weaver Michael, Lane Scott, Schmitz Joy
Faillace Department of Psychiatry and Behavioral Sciences, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX, USA.
Department of Psychology, Rice University, Houston, TX, USA.
J Addict Dis. 2024 Dec 28:1-8. doi: 10.1080/10550887.2024.2434298.
No FDA-approved medications for methamphetamine (MA) use disorder (MUD) are available. Suvorexant (SUVO), a dual orexin receptor antagonist that is FDA approved for insomnia treatment, reduces MA self-administration and MA-induced reinstatement responding in preclinical studies. SUVO may also reduce MA use by targeting substance use risk factors, including insomnia, stress, cue reactivity, and craving. This case series study assessed the (1) feasibility and safety of administering suvorexant in a sample of individuals with MUD; and (2) preliminary effects of suvorexant on objective and subjective measures of sleep, stress, and cue reactivity/craving. Participants ( = 3) were randomized to receive 1 week of SUVO or placebo using a within-subject, crossover design with a 1-week washout period between doses. Participants completed self-report (sleep quality, stress), behavioral (cold pressor task), and physiological measures (heart rate, electroencephalogram) during all three weeks. Participants wore a Fitbit to monitor sleep throughout the study. Participants completed all study visits and tasks. One report of severe drowsiness and of severe headache were made; no other severe side effects were associated with SUVO. SUVO improved total sleep time and resulted in lower resting-state alpha power, but was mixed for subjective sleep quality. SUVO administration was associated with increased overall brain reactivity to cues that was not specific to MA cues and also reduced stress, though self-reported stress demonstrated mixed results. Suvorexant was safe and tolerable in a MUD sample. Future research may benefit from investigating SUVO in a well-controlled study with a larger sample.
目前尚无美国食品药品监督管理局(FDA)批准用于治疗甲基苯丙胺(MA)使用障碍(MUD)的药物。苏沃雷生(SUVO)是一种双食欲素受体拮抗剂,已获FDA批准用于治疗失眠,在临床前研究中可减少MA的自我给药及MA诱导的复吸反应。SUVO还可能通过针对包括失眠、压力、线索反应性和渴望在内的物质使用风险因素来减少MA的使用。本病例系列研究评估了:(1)在患有MUD的个体样本中给予苏沃雷生的可行性和安全性;(2)苏沃雷生对睡眠、压力以及线索反应性/渴望的客观和主观测量指标的初步影响。3名参与者采用受试者内交叉设计,随机接受1周的SUVO或安慰剂治疗,剂量之间有1周的洗脱期。在所有三周内,参与者完成了自我报告(睡眠质量、压力)、行为(冷加压试验)和生理测量(心率、脑电图)。在整个研究过程中,参与者佩戴Fitbit来监测睡眠。参与者完成了所有的研究访视和任务。有一份关于严重嗜睡和严重头痛的报告;没有其他严重副作用与SUVO相关。SUVO改善了总睡眠时间,并导致静息状态下的α波功率降低,但主观睡眠质量的结果不一。给予SUVO与大脑对线索的整体反应性增加有关,这并非MA线索所特有,同时也减轻了压力,尽管自我报告的压力结果不一。在MUD样本中,苏沃雷生是安全且可耐受的。未来的研究可能会受益于在一个样本量更大的严格对照研究中对SUVO进行调查。