Mental Health Division P35C, Veterans Affairs Portland Health Care System, 3710 SW US Veterans Hospital Rd, Portland, OR, 97239, USA.
Department of Psychiatry, Oregon Health & Science University, Portland, OR, USA.
Psychopharmacology (Berl). 2020 Jan;237(1):263-278. doi: 10.1007/s00213-019-05364-3. Epub 2019 Oct 31.
Alcohol-use disorder (AUD) is associated with the propensity to choose smaller sooner options on the delay discounting task. It is unclear, however, how inherent risk underlies delay discounting behavior. As impulsive choice is a hallmark feature in AUD, it is important to understand the neural response to reward and delay while accounting for risk in impulsive decision-making.
This study examined activation associated with delay and reward magnitude, while controlling for risk in a probabilistic delay discounting task in AUD and examined if differences in activation were associated with treatment outcomes.
Thirty-nine recently abstinent alcohol-dependent volunteers and 46 controls completed a probabilistic delay discounting task paired with functional magnetic resonance imaging. Alcohol use was collected using a self-report journal for 3 months following baseline scan.
During delay stimulus presentations, Controls exhibited greater activation compared to the Alcohol group notably in the anterior insula, middle/dorsal anterior cingulate cortex (ACC), dorsolateral prefrontal cortex (PFC), and inferior parietal lobule. For magnitude, the Alcohol group exhibited greater activation than Controls primarily in medial PFC, rostral ACC, left posterior parietal cortex, and right precuneus. Within the Alcohol group, alcohol craving severity negatively correlated with right lateral PFC activation during reward magnitude in individuals who completed the 3-month study without relapse, while non-completers showed the opposite relationship.
The results of this study extend previous findings that alcohol use disorder is associated with differences in activation during an immediate or delayed choice by delineating activation associated with the parameters of impulsive choice.
酒精使用障碍(AUD)与在延迟折扣任务中选择更小更快选项的倾向有关。然而,内在风险如何影响延迟折扣行为尚不清楚。由于冲动选择是 AUD 的一个显著特征,因此了解冲动决策时奖励和延迟的神经反应,同时考虑风险非常重要。
本研究在 AUD 中通过概率性延迟折扣任务,在控制风险的情况下,检查了与延迟和奖励幅度相关的激活情况,并研究了激活差异是否与治疗结果相关。
39 名最近戒酒的酒精依赖志愿者和 46 名对照者完成了概率性延迟折扣任务,并进行了功能磁共振成像。使用自我报告日记在基线扫描后 3 个月内收集酒精使用情况。
在延迟刺激呈现期间,与酒精组相比,对照组在前脑岛、中/背侧前扣带回皮质(ACC)、背外侧前额叶皮质(PFC)和下顶叶区域表现出更高的激活。对于幅度,与对照组相比,酒精组主要在中脑 PFC、前扣带回头侧、左后顶叶皮质和右楔前叶表现出更高的激活。在酒精组中,在完成 3 个月无复发研究的个体中,酒精渴求严重程度与奖励幅度时右侧外侧 PFC 的激活呈负相关,而未完成者则表现出相反的关系。
这项研究的结果扩展了之前的研究结果,即酒精使用障碍与即时或延迟选择期间的激活差异有关,通过描绘与冲动选择参数相关的激活来阐明。