连接体
神经科学
相关性
认知
计算机科学
任务正网络
生物标志物
心理学
降维
默认模式网络
人类连接体项目
磁共振弥散成像
人工智能
模式识别(心理学)
人脑
人工神经网络
认知神经科学
神经网络
特征(语言学)
脑干
认知功能衰退
相似性(几何)
大脑定位
海马体
丘脑
外围设备
静息状态功能磁共振成像
神经病理学
颞叶
梯度法
网络体系结构
睡眠剥夺对认知功能的影响
生物神经网络
透视图(图形)
生物
医学
作者
Mei‐Ting Zhao,Qi Hua Gong,R. Chen,Yun Jiao,Alzheimer's Disease Neuroimaging Initiative
摘要
This investigation centered on Alzheimer's disease (AD), a progressive neurodegenerative disorder characterized by memory impairment and cognitive decline. Functional connectome gradient analysis was utilized to investigate alterations in the hierarchical architecture of brain networks in AD. The study cohort consisted of 222 subjects, encompassing 111 AD patients and 111 normal controls (NC). Connectome gradients were computed via a dimensionality reduction technique based on diffusion map embedding and analyzed at both the region of interest (ROI) and network levels. Additional connectome gradient metrics, including network median distance and gradient eccentricity, were calculated, and the relationship between connectome gradients and rich-club organization was assessed. These connectome gradient values were subsequently correlated with clinical cognitive scores. The results demonstrated a significant reduction in the principal gradient range in AD patients. At the network level, gradient values exhibited an increase in the somatomotor (SMN) and visual networks (VIS), while decreasing in the default mode (DMN) and frontoparietal networks (FPN) relative to controls. Analyzes of network mean distance and gradient eccentricity further revealed compression of the brain cortical hierarchy in AD patients. Furthermore, rich-club analyzes indicated a reduction in the gradient value difference between hub and peripheral nodes in AD patients. Finally, clinical correlation analysis revealed a positive correlation between the degree of cognitive impairment and the degree of compression of the brain cortical hierarchy. These findings provide a novel perspective on the study of brain network organization in AD patients, contributing to a more comprehensive understanding of the neural mechanisms underlying Alzheimer's disease.
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