White Augustus M, Eglovitch Michelle, Parlier-Ahmad Anna Beth, Dzierzewski Joseph M, James Morgan, Bjork James M, Moeller F Gerard, Martin Caitlin E
School of Medicine, Virginia Commonwealth University, Richmond, Virginia, United States of America.
National Sleep Foundation, Washington, DC, United States of America.
PLoS One. 2024 Jun 13;19(6):e0304461. doi: 10.1371/journal.pone.0304461. eCollection 2024.
Insomnia symptoms are negatively related to opioid use disorder (OUD) treatment outcomes, possibly reflecting the influence of sleep on neurofunctional domains implicated in addiction. Moreover, the intersection between OUD recovery and sleep represents an area well-suited for the development of novel, personalized treatment strategies. This study assessed the prevalence of clinically significant insomnia symptoms and characterized its neurofunctional correlates among a clinical sample of adults with OUD receiving buprenorphine.
Adults (N = 129) receiving buprenorphine for OUD from an outpatient clinic participated in a cross-sectional survey. Participants completed an abbreviated version of NIDA's Phenotyping Assessment Battery, which assessed 6 neurofunctional domains: sleep, negative emotionality, metacognition, interoception, cognition, and reward. Bivariate descriptive statistics compared those with evidence of clinically significant insomnia symptoms (Insomnia Severity Index [ISI] score of ≥11) to those with minimal evidence of clinically significant insomnia symptoms (ISI score of ≤10) across each of the neurofunctional domains.
Roughly 60% of participants reported clinically significant insomnia symptoms (ISI score of ≥11). Experiencing clinically significant insomnia symptoms was associated with reporting greater levels of depression, anxiety, post-traumatic stress, stress intolerance, unhelpful metacognition, and interoceptive awareness (ps<0.05). Participants with evidence of clinically significant insomnia were more likely to report that poor sleep was interfering with their OUD treatment and that improved sleep would assist with their treatment (ps<0.05).
Insomnia was prevalent among adults receiving buprenorphine for OUD. Insomnia was associated with neurofunctional performance, which may impact OUD treatment trajectories. Our findings indicate potential targets in the development of personalized treatment plans for patients with co-morbid insomnia and OUD. To inform the development of novel treatment strategies, more research is needed to understand the potential mechanistic links between sleep disturbances and substance use.
失眠症状与阿片类物质使用障碍(OUD)的治疗结果呈负相关,这可能反映了睡眠对成瘾相关神经功能领域的影响。此外,OUD康复与睡眠之间的交叉领域是开发新型个性化治疗策略的理想领域。本研究评估了接受丁丙诺啡治疗的成年OUD临床样本中具有临床意义的失眠症状的患病率,并对其神经功能相关性进行了特征描述。
来自门诊诊所接受丁丙诺啡治疗OUD的成年人(N = 129)参与了一项横断面调查。参与者完成了美国国立药物滥用研究所表型评估量表的简化版,该量表评估了6个神经功能领域:睡眠、负性情绪、元认知、内感受、认知和奖赏。双变量描述性统计比较了在每个神经功能领域中具有临床意义的失眠症状证据(失眠严重程度指数[ISI]得分≥11)的参与者与具有最小临床意义的失眠症状证据(ISI得分≤10)的参与者。
大约60%的参与者报告有具有临床意义的失眠症状(ISI得分≥11)。经历具有临床意义的失眠症状与报告更高水平的抑郁、焦虑、创伤后应激、压力不耐受、无益的元认知和内感受意识相关(p<0.05)。有临床意义的失眠证据的参与者更有可能报告睡眠不佳干扰了他们的OUD治疗,并且改善睡眠将有助于他们的治疗(p<0.05)。
失眠在接受丁丙诺啡治疗OUD的成年人中很普遍。失眠与神经功能表现相关,这可能会影响OUD的治疗轨迹。我们的研究结果指出了为共病失眠和OUD患者制定个性化治疗计划时的潜在靶点。为了为新型治疗策略的开发提供信息,需要更多的研究来了解睡眠障碍与物质使用之间的潜在机制联系。