Slower Learning Rates from Negative Outcomes in Substance Use Disorder over a 1-Year Period and their Potential Predictive Utility

Ryan Smith, S. Taylor, J. Stewart, S. Guinjoan, M. Ironside, N. Kirlic, H. Ekhtiari, Evan J. White, Haixia Zheng, R. Kuplicki, M. Paulus
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引用次数: 15

Abstract

Computational modelling is a promising approach to parse dysfunctional cognitive processes in substance use disorders (SUDs), but it is unclear how much these processes change during the recovery period. We assessed 1-year follow-up data on a sample of treatment-seeking individuals with one or more SUDs (alcohol, cannabis, sedatives, stimulants, hallucinogens, and/or opioids; N = 83) that were previously assessed at baseline within a prior computational modelling study. Relative to healthy controls (HCs; N = 48), these participants were found at baseline to show altered learning rates and less precise action selection while completing an explore-exploit decision-making task. Here we replicate these analyses when these individuals returned and re-performed the task 1 year later to assess the stability of these baseline differences. We also examine whether baseline modelling measures can predict symptoms at follow-up. Bayesian analyses indicate that: (a) group differences in learning rates were stable over time (posterior probability = 1); (b) intra-class correlations (ICCs) between model parameters at baseline and follow-up were significant and ranged from small to moderate (.25 < ICCs < .54); and (c) learning rates and/or information-seeking values at baseline were associated with substance use severity at 1-year follow-up in stimulant and opioid users (.36 < rs < .43, .002 < ps < .02). These findings suggest that learning dysfunctions are moderately stable during recovery and could correspond to trait-like vulnerability factors. In addition, computational measures at baseline had some predictive value for changes in substance use severity over time and could be clinically informative.
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1年内药物使用障碍负面结果的学习率降低及其潜在的预测效用
计算建模是解析物质使用障碍(SUD)中功能失调的认知过程的一种很有前途的方法,但尚不清楚这些过程在恢复期会发生多大变化。我们评估了一个患有一种或多种SUD(酒精、大麻、镇静剂、兴奋剂、致幻剂和/或阿片类药物;N=83)的寻求治疗个体样本的1年随访数据,这些SUD先前在先前的计算模型研究中在基线时进行了评估。与健康对照组(HC;N=48)相比,这些参与者在完成探索-开发决策任务时,在基线时表现出学习率的改变和行动选择的不太精确。在这里,当这些人返回时,我们复制了这些分析,并在一年后重新执行任务,以评估这些基线差异的稳定性。我们还研究了基线建模措施是否可以预测随访时的症状。贝叶斯分析表明:(a)学习率的群体差异随着时间的推移是稳定的(后验概率=1);(b) 基线和随访时模型参数之间的类内相关性(ICCs)显著,范围从小到中等(.25
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