Dynamic functional connectivity impairments in idiopathic rapid eye movement sleep behavior disorder

被引:11
作者
Li, Guanglu
Zhou, Liche
Chen, Zhichun
Luo, Ningdi
Niu, Mengyue
Li, Yuanyuan
Kang, Wenyan
Liu, Jun
机构
[1] Shanghai Jiao Tong Univ, Dept Neurol, Ruijin Hosp, Lu Wan Branch,Sch Med, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Inst Neurol, Ruijin Hosp, Lu Wan Branch,Sch Med, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Idiopathic rapid eye movement sleep behavior disorder; Prodromal synucleinopathy; Resting-state fMRI; Dynamic functional connectivity; Brain networks;
D O I
10.1016/j.parkreldis.2020.08.003
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Previous functional magnetic resonance imaging (fMRI) studies typically analyzed static functional connectivity (sFC) to reveal the pathophysiology of iRBD and overlooked the dynamic nature of brain activity. Thus, we aimed to explore whether iRBD showed abnormalities of brain network dynamics using the dynamic functional connectivity (dFC) approach. Methods: Resting-state fMRI data from 33 iRBD patients and 38 matched healthy controls were analyzed using an independent component analysis, sliding window correlation and k-means clustering. Relationships between clinical symptoms and abnormal dFC were evaluated using Spearman's correlation analysis. Results: Four distinct connectivity states were identified to characterize and compare dFC patterns. We demonstrated that iRBD had fewer occurrences and a shorter dwell time in the infrequent and strongly connected State 1, but with more occurrences and a longer dwell time in the frequent and sparsely connected State 2. In addition, iRBD patients showed significantly decreased FC in certain dFC states compared to healthy controls. More importantly, the impairments in the temporal properties of State 2 were found to be associated RBDSQ scores in the patient group. Conclusions: This study detected dFC impairments in iRBD patients and provided new insights into the patho-physiology of iRBD, which might contribute to the development of disease-modifying drugs in future clinical trials.
引用
收藏
页码:11 / 17
页数:7
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