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有酒精所致昏迷史的成年初期暴饮者前扣带回神经化学改变。

Altered anterior cingulate neurochemistry in emerging adult binge drinkers with a history of alcohol-induced blackouts.

作者信息

Silveri Marisa M, Cohen-Gilbert Julia, Crowley David J, Rosso Isabelle M, Jensen J Eric, Sneider Jennifer T

机构信息

Neurodevelopmental Laboratory on Addictions and Mental Health, McLean Hospital, Belmont, Massachusetts; McLean Imaging Center, McLean Hospital, Belmont, Massachusetts; Department of Psychiatry, Harvard Medical School, Boston, Massachusetts.

出版信息

Alcohol Clin Exp Res. 2014 Apr;38(4):969-79. doi: 10.1111/acer.12346. Epub 2014 Feb 11.

Abstract

BACKGROUND

Binge alcohol consumption is associated with multiple neurobiological consequences, including altered neurophysiology, brain structure, and functional activation. Magnetic resonance spectroscopy (MRS) studies have demonstrated neurochemical alterations in the frontal lobe of alcohol users, although most studies focused on older, alcohol-dependent subjects.

METHODS

In this study, neurochemical data were acquired using MRS at 4.0 Tesla from emerging adults (18 to 24 years old) who were binge alcohol drinkers (BD, n = 23) or light drinkers (LD, n = 31). Since binge drinking is also associated with increased prevalence of experiencing an alcohol-induced blackout, BD were stratified into alcohol-induced blackout (BDBO) and non-blackout (BDN) groups.

RESULTS

Overall, BD had significantly lower gamma amino-butyric acid (GABA) and N-acetyl-aspartate (NAA) in the anterior cingulate cortex (ACC) than LD. When stratified by blackout history, BDBO also had lower ACC glutamate (Glu) than LD. No group differences in MRS metabolites were observed in the parietal-occipital cortex. Lower ACC GABA and Glu remained significant after accounting for lower gray matter content in BD, however, NAA differences were no longer evident. In addition, low ACC GABA levels were associated with greater alcohol use consequences, and worse response inhibition and attention/mental flexibility in BD.

CONCLUSIONS

These data indicate that binge drinking affects frontal lobe neurochemistry, more so in those who had experienced an alcohol-induced blackout. Characterization of the neurochemical profiles associated with binge alcohol consumption and blackout history may help identify unique risk factors for the later manifestation of alcohol abuse and dependence, in young individuals who are heavy, frequent drinkers, but who do not meet the criteria for alcohol abuse disorders.

摘要

背景

暴饮酒精与多种神经生物学后果相关,包括神经生理学改变、脑结构及功能激活变化。磁共振波谱(MRS)研究已证实酒精使用者额叶存在神经化学改变,不过大多数研究聚焦于年龄较大的酒精依赖者。

方法

在本研究中,使用4.0特斯拉的MRS对18至24岁的成年饮酒者进行神经化学数据采集,这些饮酒者分为暴饮酒精者(BD,n = 23)和少量饮酒者(LD,n = 31)。由于暴饮酒精也与酒精所致黑蒙发生率增加相关,将BD组进一步分为酒精所致黑蒙组(BDBO)和非黑蒙组(BDN)。

结果

总体而言,BD组前扣带回皮质(ACC)中的γ-氨基丁酸(GABA)和N-乙酰天门冬氨酸(NAA)显著低于LD组。按黑蒙史分层后,BDBO组ACC中的谷氨酸(Glu)也低于LD组。在顶枕叶皮质未观察到各MRS代谢物的组间差异。在考虑BD组灰质含量较低的因素后,ACC中较低的GABA和Glu仍具有显著性差异,然而,NAA差异不再明显。此外,ACC中较低的GABA水平与BD组更严重的酒精使用后果、更差的反应抑制以及注意力/心理灵活性相关。

结论

这些数据表明,暴饮酒精会影响额叶神经化学,在经历过酒精所致黑蒙的人群中影响更为明显。对与暴饮酒精及黑蒙史相关的神经化学特征进行表征,可能有助于识别那些大量频繁饮酒但不符合酒精滥用障碍标准的年轻个体日后发生酒精滥用和依赖的独特危险因素。

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