Kirsch Dylan E, Tretyak Valeria, Le Vanessa, Huffman Ansley, Fromme Kim, Strakowski Stephen M, Lippard Elizabeth T C
Department of Psychiatry and Behavioral Sciences, Dell Medical School, University of Texas, Austin, TX 78712, USA.
Waggoner Center for Alcohol and Addiction Research, University of Texas, Austin, TX 78712, USA.
Behav Sci (Basel). 2022 Feb 22;12(3):57. doi: 10.3390/bs12030057.
(1) Background: Alcohol use in the course of mood disorders is associated with worse clinical outcomes. The mechanisms by which alcohol use alters the course of illness are unclear but may relate to prefrontal cortical (PFC) sensitivity to alcohol. We investigated associations between alcohol use and PFC structural trajectories in young adults with a mood disorder compared to typically developing peers. (2) Methods: 41 young adults (24 with a mood disorder, agemean = 21 ± 2 years) completed clinical evaluations, assessment of alcohol use, and two structural MRI scans approximately one year apart. Freesurfer was used to segment PFC regions of interest (ROIs) (anterior cingulate, orbitofrontal cortex, and frontal pole). Effects of group, alcohol use, time, and interactions among these variables on PFC ROIs at baseline and follow-up were modeled. Associations were examined between alcohol use and longitudinal changes in PFC ROIs with prospective mood. (3) Results: Greater alcohol use was prospectively associated with decreased frontal pole volume in participants with a mood disorder, but not typically developing comparison participants (time-by-group-by-alcohol interaction; p = 0.007); however, this interaction became a statistical trend in a sensitivity analysis excluding one outlier in terms of alcohol use. Greater alcohol use and a decrease in frontal pole volume related to longer duration of major depression during follow-up (p’s < 0.05). (4) Conclusion: Preliminary findings support more research on alcohol use, PFC trajectories, and depression recurrence in young adults with a mood disorder including individuals with heavier drinking patterns.
(1) 背景:情绪障碍病程中饮酒与更差的临床结局相关。饮酒改变疾病病程的机制尚不清楚,但可能与前额叶皮质(PFC)对酒精的敏感性有关。我们调查了患有情绪障碍的年轻人与正常发育的同龄人相比,饮酒与PFC结构轨迹之间的关联。(2) 方法:41名年轻人(24名患有情绪障碍,平均年龄 = 21 ± 2岁)完成了临床评估、饮酒情况评估以及相隔约一年的两次结构磁共振成像扫描。使用FreeSurfer对PFC感兴趣区域(ROI)(前扣带回、眶额皮质和额极)进行分割。对组、饮酒情况、时间以及这些变量之间的相互作用对基线和随访时PFC ROI的影响进行建模。研究饮酒与PFC ROI纵向变化及预期情绪之间的关联。(3) 结果:前瞻性研究发现,患有情绪障碍的参与者中,饮酒量越大与额极体积减小相关,但正常发育的对照参与者并非如此(时间×组×饮酒的交互作用;p = 0.007);然而,在一项排除一名饮酒量异常高者的敏感性分析中,这种交互作用成为一种统计学趋势。饮酒量越大和额极体积减小与随访期间重度抑郁持续时间延长有关(p值 < 0.05)。(4) 结论:初步研究结果支持对患有情绪障碍的年轻人,包括饮酒量较大者的饮酒情况、PFC轨迹和抑郁症复发进行更多研究。