基于脑电图功能连接性的阵发性运动障碍深度学习识别。

Liang Zhao, Renling Zou, Linpeng Jin
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引用次数: 0

摘要

阵发性运动障碍(PKD)是一种罕见的神经系统疾病,其特征是由突然动作引发的短暂不自主运动。由于症状与其他疾病重叠,目前的诊断方法(包括基因筛查)在识别继发性病例方面面临挑战。本研究利用静息态脑电图(EEG)功能连接矩阵和深度学习架构(AT-1CBL),介绍了一种新型 PKD 识别方法。研究使用 128 通道脑电图系统收集了 44 名 PKD 患者和 44 名健康对照组(HCs)的静息态脑电图数据。计算功能连接矩阵并将其转化为图数据,通过图理论研究 PKD 患者和对照组之间大脑网络属性的差异。通过源定位来探索患者的神经回路差异。AT-1CBL模型将1D-CNN和Bi-LSTM与注意机制相结合,在Theta波段的相位滞后指数(PLI)特征上达到了93.77%的分类准确率。图论分析表明,与普通人相比,PKD 患者大脑功能网络 Theta 波段的相位同步性明显受损,尤其是弱连接的分布。源定位分析表明,PKD 患者感觉运动区和额叶-边缘系统的功能连接差异更大,这表明运动整合异常与临床症状有关。这项研究凸显了基于脑电图功能连接的深度学习模型在准确、经济地诊断 PKD 方面的潜力,为开发用于临床监测和诊断的便携式脑电图设备提供了支持。然而,有限的数据集规模可能会影响普适性,因此有必要进一步探索多模态数据整合和先进的深度学习架构,以增强 PKD 诊断模型的稳健性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deep Learning Recognition of Paroxysmal Kinesigenic Dyskinesia Based on EEG Functional Connectivity.

Paroxysmal kinesigenic dyskinesia (PKD) is a rare neurological disorder marked by transient involuntary movements triggered by sudden actions. Current diagnostic approaches, including genetic screening, face challenges in identifying secondary cases due to symptom overlap with other disorders. This study introduces a novel PKD recognition method utilizing a resting-state electroencephalogram (EEG) functional connectivity matrix and a deep learning architecture (AT-1CBL). Resting-state EEG data from 44 PKD patients and 44 healthy controls (HCs) were collected using a 128-channel EEG system. Functional connectivity matrices were computed and transformed into graph data to examine brain network property differences between PKD patients and controls through graph theory. Source localization was conducted to explore neural circuit differences in patients. The AT-1CBL model, integrating 1D-CNN and Bi-LSTM with attentional mechanisms, achieved a classification accuracy of 93.77% on phase lag index (PLI) features in the Theta band. Graph theoretic analysis revealed significant phase synchronization impairments in the Theta band of the functional brain network in PKD patients, particularly in the distribution of weak connections compared to HCs. Source localization analyses indicated greater differences in functional connectivity in sensorimotor regions and the frontal-limbic system in PKD patients, suggesting abnormalities in motor integration related to clinical symptoms. This study highlights the potential of deep learning models based on EEG functional connectivity for accurate and cost-effective PKD diagnosis, supporting the development of portable EEG devices for clinical monitoring and diagnosis. However, the limited dataset size may affect generalizability, and further exploration of multimodal data integration and advanced deep learning architectures is necessary to enhance the robustness of PKD diagnostic models.

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