Disrupted Brain Connectivity Networks in Drug-Naive, First-Episode Major Depressive Disorder

重性抑郁障碍 毒品天真 神经科学 尾状核 默认模式网络 静息状态功能磁共振成像 神经影像学 功能磁共振成像 心理学 认知 医学 精神科 药品
作者
Junran Zhang,Jinhui Wang,Qizhu Wu,Weihong Kuang,Xiaoqi Huang,Yong He,Qiyong Gong
出处
期刊:Biological Psychiatry [Elsevier]
卷期号:70 (4): 334-342 被引量:919
标识
DOI:10.1016/j.biopsych.2011.05.018
摘要

Neuroimaging studies have shown that major depressive disorder (MDD) is accompanied by structural and functional abnormalities in specific brain regions and connections; yet, little is known about alterations of the topological organization of whole-brain networks in MDD patients.Thirty drug-naive, first-episode MDD patients and 63 healthy control subjects underwent a resting-state functional magnetic resonance imaging scan. The whole-brain functional networks were constructed by thresholding partial correlation matrices of 90 brain regions, and their topological properties (e.g., small-world, efficiency, and nodal centrality) were analyzed using graph theory-based approaches. Nonparametric permutation tests were further used for group comparisons of topological metrics.Both the MDD and control groups showed small-world architecture in brain functional networks, suggesting a balance between functional segregation and integration. However, compared with control subjects, the MDD patients showed altered quantitative values in the global properties, characterized by lower path length and higher global efficiency, implying a shift toward randomization in their brain networks. The MDD patients exhibited increased nodal centralities, predominately in the caudate nucleus and default-mode regions, including the hippocampus, inferior parietal, medial frontal, and parietal regions, and reduced nodal centralities in the occipital, frontal (orbital part), and temporal regions. The altered nodal centralities in the left hippocampus and the left caudate nucleus were correlated with disease duration and severity.These results suggest that depressive disorder is associated with disruptions in the topological organization of functional brain networks and that this disruption may contribute to disturbances in mood and cognition in MDD patients.
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