Department of Psychiatry, Washington University St. Louis Medical School, St. Louis, Missouri, USA.
Department of Psychological & Brain Sciences, Washington University St. Louis, St. Louis, Missouri, USA.
Addict Biol. 2023 Sep;28(9):e13327. doi: 10.1111/adb.13327.
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.
饮酒是一个日益严重的全球健康问题和经济负担。横断面研究可靠地表明,饮酒参与(即开始饮酒、使用、出现问题性使用、酒精使用障碍)与广泛的灰质差异有关。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,大脑结构差异也代表了酒精参与的预先存在的脆弱性因素。在这里,我们回顾了具有设计(即基于家庭的、基因组的、纵向的)的人类研究的证据,这些设计允许他们评估这些相关性反映潜在风险因素和/或酒精参与因果后果的可能性。这些研究提供了一致的证据,表明与酒精参与相关的灰质相关性在很大程度上反映了潜在的风险因素,并且有一些证据表明可能存在酒精引起的萎缩。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。一个综合模型可能是对这些数据的最佳解释,即对酒精使用的倾向影响大脑发育,而这些影响可能会因大量饮酒的神经毒性后果而加剧。