An Enhanced EEG Microstate Recognition Framework Based on Deep Neural Networks: An Application to Parkinson's Disease

被引:14
作者
Chu, Chunguang [1 ]
Zhang, Zhen [1 ]
Song, Zhenxi [2 ]
Xu, Zifan [1 ]
Wang, Jiang [1 ]
Wang, Fei [3 ]
Liu, Wei [3 ]
Lu, Liying [4 ]
Liu, Chen [1 ]
Zhu, Xiaodong [3 ]
Fietkiewicz, Chris [5 ]
Loparo, Kenneth A. [6 ]
机构
[1] Tianjin Univ, Sch Elect & Informat Engn, Tianjin 300072, Peoples R China
[2] Harbin Inst Technol, Sch Comp Sci & Technol, Shenzhen 518000, Peoples R China
[3] Tianjin Med Univ Gen Hosp, Tianjin Neurol Inst, Dept Neurol, Tianjin 300052, Peoples R China
[4] Tianjin Beichen Hosp, Dept Neurol, Tianjin 300400, Peoples R China
[5] Hobart & William Smith Coll, Dept Math & Comp Sci, Geneva, NY 14456 USA
[6] Case Western Reserve Univ, Dept Elect Engn & Comp Sci, Cleveland, OH 44106 USA
关键词
Electroencephalography; Deep learning; Neural networks; Feature extraction; Correlation; Electrodes; Scalp; Parkinson's disease; EEG microstate; enhanced recognition framework; deep neural network; activated brain regions; RESTING-STATE NETWORKS; BRAIN; CLASSIFICATION; SCHIZOPHRENIA; PREDICTION; ATTENTION;
D O I
10.1109/JBHI.2022.3232811
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Variations in brain activity patterns reveal impairments of motor and cognitive functions in the human brain. Electroencephalogram (EEG) microstates embody brain activity patterns at a microscopic time scale. However, current microstate analysis method can only recognize less than 90% of EEG signals per subject, which severely limits the characterization of dynamic brain activity. As an application to early Parkinson's disease (PD), we propose an enhanced EEG microstate recognition framework based on deep neural networks, which yields recognition rates from 90% to 99%, as accompanied by a strong anti-artifact property. Additionally, gradient-weighted class activation mapping, as a visualization technique, is employed to locate the activated functional brain regions of each microstate class. We find that each microstate class corresponds to a particular activated brain region. Finally, based on the improved identification of microstate sequences, we explore the EEG microstate characteristics and their clinical associations. We show that the decreased occurrences of a particular microstate class reflect the degree of cognitive decline in early PD, and reduced transitions between certain microstates suggest injury in motor-related brain regions. The novel EEG microstate recognition framework paves the way to revealing more effective biomarkers for early PD.
引用
收藏
页码:1307 / 1318
页数:12
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