Martin Caitlin E, Bjork James M, Keyser-Marcus Lori, Sabo Roy T, Pignatello Tiffany, Simmons Kameron, La Rosa Christina, Arias Albert J, Ramey Tatiana, Moeller F Gerard
Institute for Drug and Alcohol Studies, Virginia Commonwealth University, 203 East Cary Street, Richmond, VA 23219, USA.
Department of Psychiatry, Virginia Commonwealth University, Richmond, VA 23219, USA.
Drug Alcohol Depend Rep. 2024 Nov 22;14:100304. doi: 10.1016/j.dadr.2024.100304. eCollection 2025 Mar.
Evidence supports the common incidence of sleep disturbance in opioid use disorder (OUD) as a potential marker of disrupted orexin system functioning. This study evaluated the initial safety and tolerability of a challenge dose of lemborexant, a dual orexin antagonist, as an adjunct to buprenorphine/naloxone.
Patients (18-65 years old) with OUD receiving sublingual buprenorphine/naloxone, with a Pittsburgh Sleep Quality Index total score of 6 or higher, were recruited from outpatient clinics. After randomization, while being monitored on an inpatient research unit over two 10-hour daytime periods, participants received a placebo or lemborexant (5 mg on day one and 10 mg on day two) along with buprenorphine/naloxone. Primary outcomes included safety and tolerability: adverse events, physiologic measures, sedation level assessments. Generalized linear mixed model analysis assessed the effect of study drug and time on outcomes.
N=18 (14=male, 4=female) were randomized to lemborexant (n=12) or placebo (n=6). No unanticipated problems occurred; five adverse events occurred in the lemborexant group and two in the placebo group with no serious adverse events. None of the physiologic measures showed a significant interaction of time and placebo vs. lemborexant (5 or 10 mg): Pulse oximetry (F=0.6; p=0.84), End-tidal CO2 (F=0.5; p=0.91), Heart rate (F=0.6; p=0.82), Systolic blood pressure (F=0.7; p=0.73), Diastolic blood pressure (F=2.0; p=0.06). At 9 hours after study drug administration, all participants returned to baseline sedation levels and were discharged.
Findings support the initial safety and tolerability of lemborexant as an adjunctive treatment for insomnia in humans receiving buprenorphine for OUD. Future longitudinal work is warranted with larger samples.
有证据表明,阿片类物质使用障碍(OUD)患者中睡眠障碍很常见,这可能是食欲素系统功能紊乱的一个潜在标志。本研究评估了双重食欲素拮抗剂伦索思坦挑战剂量作为丁丙诺啡/纳洛酮辅助用药的初始安全性和耐受性。
从门诊招募年龄在18至65岁、接受舌下丁丙诺啡/纳洛酮治疗且匹兹堡睡眠质量指数总分≥6的OUD患者。随机分组后,在住院研究单元进行两个10小时白天时段的监测期间,参与者接受安慰剂或伦索思坦(第1天5毫克,第2天10毫克)以及丁丙诺啡/纳洛酮。主要结局包括安全性和耐受性:不良事件、生理指标、镇静水平评估。广义线性混合模型分析评估研究药物和时间对结局的影响。
18名患者(14名男性,4名女性)被随机分为伦索思坦组(n = 12)或安慰剂组(n = 6)。未出现意外问题;伦索思坦组发生5起不良事件,安慰剂组发生2起,均无严重不良事件。生理指标中,时间与安慰剂对比伦索思坦(5或10毫克)均未显示显著交互作用:脉搏血氧饱和度(F = 0.6;p = 0.84)、呼气末二氧化碳(F = 0.5;p = 0.91)、心率(F = 0.6;p = 0.82)、收缩压(F = 0.7;p = 0.73)、舒张压(F = 2.0;p = 0.06)。给药后9小时,所有参与者均恢复至基线镇静水平并出院。
研究结果支持伦索思坦作为接受丁丙诺啡治疗OUD患者失眠辅助治疗的初始安全性和耐受性。未来有必要用更大样本进行纵向研究。