Alcohol use and grey matter structure: Disentangling predispositional and causal contributions in human studies

IF 3.1 3区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
David A. A. Baranger, Sarah E. Paul, Alexander S. Hatoum, Ryan Bogdan
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引用次数: 0

Abstract

Alcohol use is a growing global health concern and economic burden. Alcohol involvement (i.e., initiation, use, problematic use, alcohol use disorder) has been reliably associated with broad spectrum grey matter differences in cross-sectional studies. These findings have been largely interpreted as reflecting alcohol-induced atrophy. However, emerging data suggest that brain structure differences also represent pre-existing vulnerability factors for alcohol involvement. Here, we review evidence from human studies with designs (i.e., family-based, genomic, longitudinal) that allow them to assess the plausibility that these correlates reflect predispositional risk factors and/or causal consequences of alcohol involvement. These studies provide convergent evidence that grey matter correlates of alcohol involvement largely reflect predisposing risk factors, with some evidence for potential alcohol-induced atrophy. These conclusions highlight the importance of study designs that can provide causal clues to cross-sectional observations. An integrative model may best account for these data, in which predisposition to alcohol use affects brain development, effects which may then be compounded by the neurotoxic consequences of heavy alcohol use.

Abstract Image

酒精使用和灰质结构:人类研究中纠缠的倾向和因果关系。
饮酒是一个日益严重的全球健康问题和经济负担。在横断面研究中,酒精参与(即引发、使用、有问题的使用、酒精使用障碍)与广泛的灰质差异可靠相关。这些发现在很大程度上被解释为反映了酒精引起的萎缩。然而,新出现的数据表明,大脑结构的差异也代表了酒精参与的预先存在的脆弱因素。在这里,我们回顾了人类研究的证据,这些研究的设计(即基于家庭的、基因组的、纵向的)使他们能够评估这些相关性反映易感风险因素和/或酒精参与的因果后果的合理性。这些研究提供了一致的证据,表明酒精参与的灰质相关性在很大程度上反映了易感风险因素,并有一些证据表明潜在的酒精诱导的萎缩。这些结论强调了能够为横断面观察提供因果线索的研究设计的重要性。综合模型可能最能解释这些数据,在这些数据中,饮酒倾向会影响大脑发育,而大量饮酒的神经毒性后果可能会加剧这种影响。
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 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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