Abnormal Baseline Brain Activity in Parkinson's Disease With and Without REM Sleep Behavior Disorder: A Resting-State Functional MRI Study

被引:48
作者
Li, Dan [1 ,2 ]
Huang, Peiyu [3 ]
Zang, Yufeng [4 ]
Lou, Yuting [1 ]
Cen, Zhidong [1 ]
Gu, Quanquan [3 ]
Xuan, Min [3 ]
Xie, Fei [1 ]
Ouyang, Zhiyuan [1 ]
Wang, Bo [1 ]
Zhang, Minming [3 ]
Luo, Wei [1 ]
机构
[1] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Neurol, 88 Jiefang Rd, Hangzhou 310009, Zhejiang, Peoples R China
[2] First Peoples Hosp Nantong, Dept Neurol, Nantong, Peoples R China
[3] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Radiol, Hangzhou, Zhejiang, Peoples R China
[4] Hangzhou Normal Univ, Ctr Cognit & Brain Disorders, Hangzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
PERFUSION; CONNECTIVITY; PROGRESSION; CIRCUITS; COMPLEX; FMRI;
D O I
10.1002/jmri.25571
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: To investigate the differences in spontaneous brain activity between Parkinson's disease (PD) patients with rapid eye movement sleep behavior disorder (RBD), PD patients without RBD, and normal controls, which may shed new light on the neural mechanism of RBD. Materials and Methods: Eighteen PD patients with RBD, 16 patients without RBD, and 19 age- and gender-matched normal controls underwent clinical assessment and functional magnetic resonance imaging (fMRI) with a 3.0T scanner. Resting-state fMRI scans were collected using an echo planar imaging sequence. Amplitude of low-frequency fluctuations (ALFF) were calculated to measure spontaneous brain activity in each subject. Results: Compared with PD patients without RBD, patients with RBD exhibited significantly decreased ALFF values (P < 0.001, cluster level) in primary motor cortex extending to premotor cortex. Compared with normal controls, PD patients exhibited decreased ALFF values (P < 0.001, cluster level) in caudate and putamen (P < 0.001, cluster level), and increased ALFF values (P = 0.03, cluster level) in prefrontal cortex. Conclusion: The altered spontaneous brain activity in motor cortex may contribute to the pathogenesis of RBD in PD patients, which further supports the idea that the pathophysiology of RBD involves not only midbrain dysfunction but also cerebral cortex abnormalities. Our findings provide additional insight into the neural mechanism of RBD and may drive future research to develop better treatment.
引用
收藏
页码:697 / 703
页数:7
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