P3 事件相关电位 (ERP) 对酒精线索的反应对生态评估酒精渴求和使用的预测作用

IF 3.1 3区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Casey B. Kohen, Roberto U. Cofresí, Thomas M. Piasecki, Bruce D. Bartholow
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引用次数: 0

摘要

酒精线索激励显著性的神经测量与更危险的饮酒行为和主观反应特征的回顾性报告有关。本研究测试了酒精相关线索引起的 P3 事件相关电位(ERP)(ACR-P3)是否能预测真实世界饮酒事件中的酒精使用和渴求。参与者(N = 262;Mage = 19.53;56% 为女性)完成了一项实验室任务,即在记录脑电图的同时观看日常物品(Neutral)、非酒精饮料(NonAlc)和酒精饮料(Alc)的图像,然后完成一项为期 21 天的生态瞬间评估(EMA)方案,其中记录了他们对酒精的渴望和消费情况。在整个饮酒过程中,使用人体测量法得出估计血液酒精浓度(eBAC)。多层次建模表明,所有刺激引起的P3振幅与事件内酒精使用测量(如eBAC、累计饮酒量)之间存在正相关。重点跟踪分析表明,AlcP3 振幅与发作内 eBAC 之间存在正相关:较大的 AlcP3 与 eBAC 的陡峭上升有关。这种关联在控制 NonAlcP3 与 eBAC 之间的关联后仍很稳健。AlcP3 还与发作水平测量(如最大饮酒量、最大 eBAC)呈正相关。任何 P3 变量与基于 EMA 的渴求测量之间都没有关联。因此,酒精线索激励显著性神经测量的个体差异似乎可以预测酒精消费的速度和强度,但不能预测真实世界酒精使用事件中的渴求报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Predictive utility of the P3 event-related potential (ERP) response to alcohol cues for ecologically assessed alcohol craving and use

Predictive utility of the P3 event-related potential (ERP) response to alcohol cues for ecologically assessed alcohol craving and use

Predictive utility of the P3 event-related potential (ERP) response to alcohol cues for ecologically assessed alcohol craving and use

Neural measures of alcohol cue incentive salience have been associated with retrospective reports of riskier alcohol use behaviour and subjective response profiles. This study tested whether the P3 event-related potential (ERP) elicited by alcohol-related cues (ACR-P3) can forecast alcohol use and craving during real-world drinking episodes. Participants (N = 262; Mage = 19.53; 56% female) completed a laboratory task in which they viewed images of everyday objects (Neutral), non-alcohol drinks (NonAlc) and alcohol beverages (Alc) while EEG was recorded and then completed a 21-day ecological momentary assessment (EMA) protocol in which they recorded alcohol craving and consumption. Anthropometrics were used to derive estimated blood alcohol concentration (eBAC) throughout drinking episodes. Multilevel modelling indicated positive associations between P3 amplitudes elicited by all stimuli and within-episode alcohol use measures (e.g., eBAC, cumulative drinks). Focal follow-up analyses indicated a positive association between AlcP3 amplitude and eBAC within episodes: Larger AlcP3 was associated with a steeper rise in eBAC. This association was robust to controlling for the association between NonAlcP3 and eBAC. AlcP3 also was positively associated with episode-level measures (e.g., max drinks, max eBAC). There were no associations between any P3 variables and EMA-based craving measures. Thus, individual differences in neural measures of alcohol cue incentive salience appear to predict the speed and intensity of alcohol consumption but not reports of craving during real-world alcohol use episodes.

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来源期刊
Addiction Biology
Addiction Biology 生物-生化与分子生物学
CiteScore
8.10
自引率
2.90%
发文量
118
审稿时长
6-12 weeks
期刊介绍: Addiction Biology is focused on neuroscience contributions and it aims to advance our understanding of the action of drugs of abuse and addictive processes. Papers are accepted in both animal experimentation or clinical research. The content is geared towards behavioral, molecular, genetic, biochemical, neuro-biological and pharmacology aspects of these fields. Addiction Biology includes peer-reviewed original research reports and reviews. Addiction Biology is published on behalf of the Society for the Study of Addiction to Alcohol and other Drugs (SSA). Members of the Society for the Study of Addiction receive the Journal as part of their annual membership subscription.
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