Reward Sensitivity in Patients Receiving Opioid Agonist and Antagonist Treatment for Opioid Use Disorder: An Observational Study.

Martin Trøstheim, Mads Lund Pedersen, Siri Leknes, Lennja Majid Hama, Mathias Nikolai Roland, Philipp Paul Lobmaier, Kristin Klemmetsby Solli, Bente M Weimand, Lars Tanum, Marie Eikemo
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Abstract

Background: Disrupted reward processing is a core component in neurobiological theories of addictions, including opioid use disorder (OUD). While acute opioid agonist and antagonist administration can modulate reward behavior and experiences, it remains unclear how typical long-term OUD treatment with these medications impact patients' sensitivity to substance-free rewards. We therefore conducted a cross-sectional study of reward sensitivity in opioid agonist- and antagonist-treated OUD patients, and healthy volunteers.

Methods: Ninety-six OUD patients on extended-release naltrexone (n=45) or opioid agonists (n=51) and 50 healthy volunteers completed a probabilistic reward task (PRT) and self-report measures of anhedonia, depression, preoccupation with immediate consequences, substance craving and life satisfaction in a single session. We used signal detection analysis and drift diffusion modeling to derive behavioral reward bias measures from PRT performance. Group differences were modeled with beta and linear regression.

Results: Patients reported significantly greater anhedonia (Cohen's ds≥0.64), depression (ds≥0.53) and preoccupation with immediate consequences (ds≥0.54) than heathy volunteers, but differences between naltrexone- and opioid agonist-treated patients were non-significant (ds≤0.26). Group differences in behavioral reward bias were small and non-significant (ps=1, BF01s≥84.13). Anhedonia was significantly associated with lower life satisfaction (OR [95% CI]=1.10 [1.04, 1.17]). There were no other significant associations between reward sensitivity measures and life satisfaction or craving (ps≥0.31, BF01s≥2.58).

Conclusion: These data support an association between OUD and reduced well-being irrespective of opioid agonist or antagonist treatment, highlighting patients' need for psychosocial support and/or adjunct interventions. Major detrimental effects of naltrexone treatment on well-being seem unlikely from these and previous results.

阿片类药物使用障碍患者接受阿片类药物激动剂和拮抗剂治疗的奖励敏感性:一项观察性研究。
背景:中断的奖励加工是成瘾的神经生物学理论的核心组成部分,包括阿片类药物使用障碍(OUD)。虽然急性阿片类激动剂和拮抗剂可以调节奖励行为和体验,但目前尚不清楚这些药物的典型长期OUD治疗如何影响患者对无物质奖励的敏感性。因此,我们对阿片类激动剂和拮抗剂治疗的OUD患者和健康志愿者的奖励敏感性进行了横断面研究。方法:96例服用缓释纳曲酮(n=45)或阿片类激动剂(n=51)的OUD患者和50名健康志愿者在一次疗程中完成了概率奖励任务(PRT)和自我报告的快感缺乏、抑郁、即刻后果的关注、物质渴望和生活满意度。我们使用信号检测分析和漂移扩散模型从PRT的表现中得出行为奖励偏差的度量。组间差异采用beta和线性回归建模。结果:与健康志愿者相比,患者报告的快感缺乏症(Cohen’s ds≥0.64)、抑郁(ds≥0.53)和关注即刻后果(ds≥0.54)显著增加,但纳曲酮和阿片类激动剂治疗患者之间的差异无统计学意义(ds≤0.26)。行为奖励偏差组间差异不显著(ps=1, BF01s≥84.13)。快感缺乏与较低的生活满意度显著相关(OR [95% CI]=1.10[1.04, 1.17])。奖励敏感性测量与生活满意度或渴望之间无其他显著相关(ps≥0.31,BF01s≥2.58)。结论:这些数据支持不考虑阿片类药物激动剂或拮抗剂治疗的OUD和幸福感下降之间的关联,强调患者需要社会心理支持和/或辅助干预。从这些和以前的结果来看,纳曲酮治疗对健康的主要有害影响似乎不太可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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