Abnormal voxel-wise whole-brain functional connectivity in first-episode, drug-naïve adolescents with major depression disorder

楔前 重性抑郁障碍 海马体 心理学 体素 萧条(经济学) 功能磁共振成像 神经科学 前额叶皮质 毒品天真 静息状态功能磁共振成像 海马旁回 脑岛 额上回 精神科 医学 扁桃形结构 颞叶 认知 药品 癫痫 经济 宏观经济学 放射科
作者
Ruiping Zheng,Yuan Chen,Yu Jiang,Bingqian Zhou,Shaoqiang Han,Yarui Wei,Caihong Wang,Jingliang Cheng
出处
期刊:European Child & Adolescent Psychiatry [Springer Science+Business Media]
卷期号:32 (7): 1317-1327 被引量:21
标识
DOI:10.1007/s00787-022-01959-y
摘要

Major depression disorder (MDD) is one of the most common psychiatric disorders. Previous studies have demonstrated structural and functional abnormalities in adult depression. However, the neurobiology of adolescent depression has not been fully understood. The aim of this study was to investigate the intrinsic dysconnectivity pattern of voxel-level whole-brain functional networks in first-episode, drug-naïve adolescents with MDD. Resting-state functional magnetic resonance imaging data were acquired from 66 depressed adolescents and 47 matched healthy controls. Voxel-wise degree centrality (DC) analysis was performed to identify voxels that showed altered whole-brain functional connectivity (FC) with other voxels. We further conducted seed-based FC analysis to investigate in more detail the connectivity patterns of the identified DC changes. The relationship between altered DC and clinical variables in depressed adolescents was also analyzed. Compared with controls, depressed adolescents showed lower DC in the bilateral hippocampus, left superior temporal gyrus and right insula. Seed-based analysis revealed that depressed adolescents, relative to controls, showed hypoconnectivity between the hippocampus to the medial prefrontal regions and right precuneus. Furthermore, the DC values in the bilateral hippocampus were correlated with the Hamilton Depression Rating Scale score and duration of disease (all P < 0.05, false discovery rate corrected). Our study indicates abnormal intrinsic dysconnectivity patterns of whole-brain functional networks in drug-naïve, first-episode adolescents with MDD, and abnormal DC in the hippocampus may affect the association of prefrontal-hippocampus circuit. These findings may provide new insights into the pathophysiology of adolescent-onset MDD.
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