Mesocorticolimbic system reactivity to alcohol use-related visual cues as a function of alcohol sensitivity phenotype: A pilot fMRI study

Roberto U. Cofresí , Spencer Upton , Alexander A. Brown , Thomas M. Piasecki , Bruce D. Bartholow , Brett Froeliger
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Abstract

Low sensitivity (LS) to alcohol is a risk factor for alcohol use disorder (AUD). Compared to peers with high sensitivity (HS), LS individuals drink more, report more problems, and exhibit potentiated alcohol cue reactivity (ACR). Heightened ACR suggests LS confers AUD risk via incentive sensitization, which is thought to take place in the mesocorticolimbic system. This study examined neural ACR in LS and HS individuals. Young adults (N = 32, Mage=20.3) were recruited based on the Alcohol Sensitivity Questionnaire (HS: n = 16; LS: n = 16; 9 females/group). Participants completed an event-related fMRI ACR task. Group LS had higher ACR in left ventrolateral prefrontal cortex than group HS. In group LS, ACR in left caudomedial orbitofrontal cortex or left putamen was low at low alcohol use levels and high at heavier or more problematic alcohol use levels, whereas the opposite was true in group HS. Alcohol use level also was associated with the level of ACR in left substantia nigra among males in group LS. Taken together, results suggest elevated mesocorticolimbic ACR among LS individuals, especially those using alcohol at hazardous levels. Future studies with larger samples are warranted to determine the neurobiological loci underlying LS-based amplified ACR and AUD risk.

中脑皮层边缘系统对酒精使用相关视觉线索的反应与酒精敏感表型的关系:一项试验性 fMRI 研究
对酒精的低敏感度(LS)是导致酒精使用障碍(AUD)的一个危险因素。与酒精敏感度高(HS)的同龄人相比,酒精敏感度低的人饮酒更多,报告的问题更多,并表现出强化的酒精线索反应性(ACR)。增强的 ACR 表明,LS 会通过激励敏感化带来 AUD 风险,而激励敏感化被认为发生在中皮质边缘系统。本研究检测了 LS 和 HS 患者的神经 ACR。研究人员根据酒精敏感性问卷招募了年轻的成年人(32 人,平均年龄 20.3 岁)(HS:16 人;LS:16 人;每组 9 名女性)。参与者完成了与事件相关的 fMRI ACR 任务。与 HS 组相比,LS 组左侧腹外侧前额叶皮层的 ACR 更高。在 LS 组中,左侧尾内侧眶额叶皮层或左侧丘脑的 ACR 在酒精使用水平低时较低,而在酒精使用水平较高或问题较多时较高,而 HS 组则相反。在 LS 组男性中,酒精使用水平也与左侧黑质的 ACR 水平有关。综上所述,研究结果表明,LS 组人群,尤其是酗酒程度严重的人群,中皮质边缘 ACR 水平升高。未来有必要对更大样本进行研究,以确定基于LS的ACR放大和AUD风险的神经生物学位点。
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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来源期刊
Addiction neuroscience
Addiction neuroscience Neuroscience (General)
CiteScore
1.30
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0.00%
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审稿时长
118 days
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