Simmatis Leif Er, Russo Emma E, Steininger Tayo, Riddell Haleigh, Chen Evelyn, Chiu Queenny, Lin Michelle, Oh Donghun, Taheri Porsha, Harmsen Irene E, Samuel Nardin
Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Cove Neurosciences Inc., Toronto, Ontario, Canada.
J Alzheimers Dis. 2025 Mar 18:13872877251327754. doi: 10.1177/13872877251327754.
BackgroundAlzheimer's disease (AD) is a neurodegenerative disorder that profoundly alters brain function and organization. Currently, there is a lack of validated functional biomarkers to aid in diagnosing and classifying AD. Therefore, there is a pressing need for early, accurate, non-invasive, and accessible methods to detect and characterize disease progression. Electroencephalography (EEG) has emerged as a minimally invasive technique to quantify functional changes in neural activity associated with AD. However, challenges such as poor signal-to-noise ratio-particularly for resting-state (rsEEG) recordings-and issues with standardization have hindered its broader application.ObjectiveTo conduct a pilot analysis of our custom automated preprocessing and feature extraction pipeline to identify indicators of AD and correlates of disease progression.MethodsWe analyzed data from 36 individuals with AD and 29 healthy participants recorded using a standard 19-channel EEG and features were processed using our custom end-t-end pipeline. Various features encompassing amplitude, power, connectivity, complexity, and microstates were extracted. Unsupervised machine learning (uniform manifold approximation and projection) and supervised learning (random forest classifiers with nested cross-validation) were used to characterize the dataset and identify differences between AD and healthy groups.ResultsOur pipeline successfully detected several new and previously established EEG-based measures indicative of AD status and progression, demonstrating strong external validity.ConclusionsOur findings suggest that this automated approach provides a promising initial framework for implementing EEG biomarkers in the AD patient population, paving the way for improved diagnostic and monitoring strategies.
背景
阿尔茨海默病(AD)是一种神经退行性疾病,会深刻改变大脑功能和结构。目前,缺乏经过验证的功能性生物标志物来辅助AD的诊断和分类。因此,迫切需要早期、准确、非侵入性且可及的方法来检测和描述疾病进展。脑电图(EEG)已成为一种微创技术,用于量化与AD相关的神经活动功能变化。然而,诸如信噪比差(尤其是静息态(rsEEG)记录)以及标准化问题等挑战阻碍了其更广泛的应用。
目的
对我们定制的自动预处理和特征提取流程进行初步分析,以识别AD的指标和疾病进展的相关因素。
方法
我们分析了36名AD患者和29名健康参与者使用标准19通道脑电图记录的数据,并使用我们定制的端到端流程对特征进行处理。提取了包括幅度、功率、连通性、复杂性和微状态在内的各种特征。使用无监督机器学习(均匀流形近似和投影)和监督学习(带有嵌套交叉验证的随机森林分类器)来描述数据集并识别AD组和健康组之间的差异。
结果
我们的流程成功检测到了几种新的以及先前已确定的基于脑电图的指标,这些指标表明了AD的状态和进展,具有很强的外部效度。
结论
我们的研究结果表明,这种自动化方法为在AD患者群体中实施脑电图生物标志物提供了一个有前景的初始框架,为改进诊断和监测策略铺平了道路。