Duke-UNC Brain Imaging and Analysis Center, Duke University, Durham, NC, USA.
VA Mid-Atlantic MIRECC, Durham VA Medical Center, Durham VA, Durham, NC, USA.
Neuropsychopharmacology. 2023 Jan;48(2):317-326. doi: 10.1038/s41386-022-01457-4. Epub 2022 Oct 8.
Cortical thickness changes dramatically during development and is associated with adolescent drinking. However, previous findings have been inconsistent and limited by region-of-interest approaches that are underpowered because they do not conform to the underlying spatially heterogeneous effects of alcohol. In this study, adolescents (n = 657; 12-22 years at baseline) from the National Consortium on Alcohol and Neurodevelopment in Adolescence (NCANDA) study who endorsed little to no alcohol use at baseline were assessed with structural magnetic resonance imaging and followed longitudinally at four yearly intervals. Seven unique spatial patterns of covarying cortical thickness were obtained from the baseline scans by applying an unsupervised machine learning method called non-negative matrix factorization (NMF). The cortical thickness maps of all participants' longitudinal scans were projected onto vertex-level cortical patterns to obtain participant-specific coefficients for each pattern. Linear mixed-effects models were fit to each pattern to investigate longitudinal effects of alcohol consumption on cortical thickness. We found in six NMF-derived cortical thickness patterns, the longitudinal rate of decline in no/low drinkers was similar for all age cohorts. Among moderate drinkers the decline was faster in the younger adolescent cohort and slower in the older cohort. Among heavy drinkers the decline was fastest in the younger cohort and slowest in the older cohort. The findings suggested that unsupervised machine learning successfully delineated spatially coordinated patterns of vertex-level cortical thickness variation that are unconstrained by neuroanatomical features. Age-appropriate cortical thinning is more rapid in younger adolescent drinkers and slower in older adolescent drinkers, an effect that is strongest among heavy drinkers.
皮质厚度在发育过程中会发生剧烈变化,并且与青少年饮酒有关。然而,之前的研究结果不一致,并且受到了基于感兴趣区域的方法的限制,这些方法的效力不足,因为它们不符合酒精潜在的空间异质效应。在这项研究中,来自青少年酒精与神经发育全国合作研究组织(NCANDA)的青少年(n=657;基线时年龄为 12-22 岁),他们在基线时报告很少或没有饮酒,通过结构磁共振成像进行了评估,并在四年的时间间隔内进行了纵向随访。通过应用一种称为非负矩阵分解(NMF)的无监督机器学习方法,从基线扫描中获得了七个独特的皮质厚度协变空间模式。所有参与者的纵向扫描的皮质厚度图都被投射到顶点水平的皮质模式上,以获得每个模式的参与者特异性系数。线性混合效应模型被拟合到每个模式中,以研究饮酒对皮质厚度的纵向影响。我们在六个 NMF 衍生的皮质厚度模式中发现,在所有年龄组中,不饮酒或低饮酒者的纵向下降率相似。在中度饮酒者中,年轻青少年组下降速度较快,而年龄较大的青少年组下降速度较慢。在重度饮酒者中,年轻青少年组下降速度最快,年龄较大的青少年组下降速度最慢。研究结果表明,无监督机器学习成功描绘了顶点水平皮质厚度变化的空间协调模式,不受神经解剖特征的限制。在年轻青少年饮酒者中,年龄适当的皮质变薄速度更快,在年龄较大的青少年饮酒者中速度更慢,而在重度饮酒者中,这种效应最强。