Wu Yunfan, Zhou Zhihua, Fu Shishun, Zeng Shaoqing, Ma Xiaofen, Fang Jin, Yang Ning, Li Chao, Yin Yi, Hua Kelei, Liu Mengchen, Li Guomin, Yu Kanghui, Jiang Guihua
Department of Medical Imaging, Guangdong Second Provincial General Hospital, Guangzhou, China.
Department of Neurology, The First Affiliated Hospital, School of Clinical Medicine of Guangdong Pharmaceutical University, Guangzhou, China.
Front Psychiatry. 2020 Apr 23;11:308. doi: 10.3389/fpsyt.2020.00308. eCollection 2020.
Insomnia is the most prevalent sleep complaint in the general population but is often intractable due to uncertainty regarding the underlying pathomechanisms. Sleep is regulated by a network of neural structures interconnected with the core nodes of the brain connectome referred to as the "rich club". We examined alterations in brain rich-club organization as revealed by diffusion tensor imaging (DTI) and the statistical relationships between abnormalities in rich-club metrics and the clinical features of primary insomnia (PI).
This study recruited 43 primary insomnia (PI) patients and 42 age-, sex-, and education level-matched healthy controls (HCs). Differences in global and regional network parameters between PI and healthy control groups were compared by nonparametric tests, and Spearman's correlations were calculated to assess associations of these network metrics with PI-related clinical features, including disease duration and scores on the Pittsburgh Sleep Quality Index, Insomnia Severity Index, Self-Rating Anxiety Scale, and Self-Rating Depression Scale.
Weighted white matter networks exhibited weaker rich-club organization in PI patients than HCs across different thresholds (50%, 75%, and 90%) and parcellation schemes [automated anatomical labeling (AAL)-90 and AAL-1024]. Aberrant rich-club organization was found mainly in limbic-cortical-basal ganglia circuits and the default-mode network.
Abnormal rich-club metrics are a characteristic feature of PI-related to disease severity. These metrics provide potential clues to PI pathogenesis and may be useful as diagnostic markers and for assessment of treatment response.
失眠是普通人群中最常见的睡眠问题,但由于潜在病理机制尚不确定,往往难以治疗。睡眠由与大脑连接组的核心节点相互连接的神经结构网络调节,这些核心节点被称为“富集俱乐部”。我们通过扩散张量成像(DTI)研究了大脑富集俱乐部组织的改变,以及富集俱乐部指标异常与原发性失眠(PI)临床特征之间的统计关系。
本研究招募了43例原发性失眠(PI)患者和42名年龄、性别和教育水平相匹配的健康对照(HCs)。通过非参数检验比较PI组和健康对照组之间全局和区域网络参数的差异,并计算Spearman相关性,以评估这些网络指标与PI相关临床特征的关联,包括病程以及匹兹堡睡眠质量指数、失眠严重程度指数、自评焦虑量表和自评抑郁量表的得分。
在不同阈值(50%、75%和90%)和脑区划分方案[自动解剖标记(AAL)-90和AAL-1024]下,PI患者的加权白质网络富集俱乐部组织比HCs弱。异常的富集俱乐部组织主要见于边缘-皮质-基底神经节回路和默认模式网络。
异常的富集俱乐部指标是PI与疾病严重程度相关的特征。这些指标为PI的发病机制提供了潜在线索,可能作为诊断标志物和评估治疗反应有用。