Time-Frequency Complexity Maps for EEG-Based Diagnosis of Alzheimer's Disease Using a Lightweight Deep Neural Network

被引:5
作者
Polat, Hasan [1 ]
机构
[1] Bingol Univ, Dept Elect & Energy, TR-12000 Bingol, Turkey
关键词
Alzheimer' disease; EEG; deep learning; entropy; MobileNet; complexity; PERMUTATION ENTROPY; FEATURES;
D O I
10.18280/ts.390623
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
Alzheimer's disease (AD) is a neurodegenerative disorder with an unknown etiology and a significant prevalence. Rapid and accurate detection of AD is crucial to assist in a more effective and tailored treatment plan to delay the progression of the disease. This paper introduces a novel approach based on a time-frequency complexity map (complextrogram) for the automated AD diagnosis. The complextrogram is the topographic complexity level of an EEG signal, plotted as a function of time and frequency. The complextrogram representations were fed into a well-known lightweight deep neural network called MobileNet for robust performance on resource and accuracy tradeoffs. The experiments were performed using a five-fold cross-validation technique on a publicly available database containing clinical EEG recordings from 24 patients with AD and 24 healthy, age-matched controls. The proposed pipeline provided competitive performance with just 2.2 M parameters and achieved the best overall accuracy for some locations in the frontal lobes (Fp2 and F8 channels). For both channels, the classification accuracy was 100%. Also, the violin plot was used to get further details of the distribution of complexity values for specific frequency rhythms. After statistical evaluation, it was observed that neurodegenerative conditions caused changes in chaotic behaviors, including increased delta complexity and decreased alpha complexity. Results demonstrated that the complextrogram representation proved its potency for the input quality required by the deep learning architectures. Furthermore, the complextrogram method is a promising pathway to discriminate and reflect the fundamental characteristics of AD abnormalities.
引用
收藏
页码:2103 / 2113
页数:11
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