有酗酒风险的年轻人对威胁和奖励的神经反应。

IF 3.1 3区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Katelyn T. Kirk-Provencher, Rosa H. Hakimi, Keinada Andereas, Anne E. Penner, Joshua L. Gowin
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引用次数: 0

摘要

酒精使用障碍(AUD)具有遗传性。因此,与无家族史的人相比,有阳性家族史的年轻成年人是高危群体,如果在两组人饮酒水平相似的时候进行研究,就有机会确定与 AUD 风险相关的神经处理模式。以前的研究表明,对潜在奖励的反应减弱与 AUD 遗传风险有关,但目前还不清楚威胁是如何调节这种反应的。我们在 fMRI 过程中使用了改良的货币激励延迟任务,以有(n = 31)和无(n = 44)有害酒精使用家族史的年轻成人为样本,研究威胁与奖励预期之间相互作用的神经相关性。我们发现,在右侧伏隔核中,线索和组别之间存在相互作用(p = 0.048),其中家族史阳性组别对获得 5 美元和失去 5 美元的预期与获得 0 美元的预期之间的差异较小;家族史阳性组别对获得 5 美元和失去 5 美元的预期与获得 0 美元的预期之间的差异也较小(p 0.70)。通过神经和行为标记对潜在奖赏和消极后果的奖赏处理可能会减弱。在这个阶段,神经对威胁的反应可能不是导致风险的因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Neural response to threat and reward among young adults at risk for alcohol use disorder

Neural response to threat and reward among young adults at risk for alcohol use disorder

Alcohol use disorder (AUD) is heritable. Thus, young adults with positive family histories represent an at-risk group relative to those without a family history, and if studied at a time when both groups have similar levels of alcohol use, it provides an opportunity to identify neural processing patterns associated with risk for AUD. Previous studies have shown that diminished response to potential reward is associated with genetic risk for AUD, but it is unclear how threat may modulate this response. We used a modified Monetary Incentive Delay task during fMRI to examine neural correlates of the interaction between threat and reward anticipation in a sample of young adults with (n = 31) and without (n = 44) family histories of harmful alcohol use. We found an interaction (p = 0.048) between cue and group in the right nucleus accumbens where the family history positive group showed less differentiation to the anticipation of gaining $5 and losing $5 relative to gaining $0. The family history-positive group also reported less excitement for trials to gain $5 relative to gaining $0 (p < 0.001). Family history-positive individuals showed less activation in the left insula during both safe and threat blocks compared to family history-negative individuals (p = 0.005), but the groups did not differ as a function of threat (p > 0.70). Young adults with, relative to without, enriched risk for AUD may have diminished reward processing via both neural and behavioural markers to potential rewarding and negative consequences. Neural response to threat may not be a contributing factor to risk at this stage.

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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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