Al-Nuaimi Ali H, Blūma Marina, Al-Juboori Shaymaa S, Eke Chima S, Jammeh Emmanuel, Sun Lingfen, Ifeachor Emmanuel
School of Engineering, Computing and Mathematics, Faculty of Science and Engineering, University of Plymouth, Drake Circus, Plymouth PL4 8AA, UK.
College of Education for Pure Science (Ibn Al-Haitham), University of Baghdad, Al Adhamiya, Baghdad 10053, Iraq.
Brain Sci. 2021 Jul 31;11(8):1026. doi: 10.3390/brainsci11081026.
Biomarkers to detect Alzheimer's disease (AD) would enable patients to gain access to appropriate services and may facilitate the development of new therapies. Given the large numbers of people affected by AD, there is a need for a low-cost, easy to use method to detect AD patients. Potentially, the electroencephalogram (EEG) can play a valuable role in this, but at present no single EEG biomarker is robust enough for use in practice. This study aims to provide a methodological framework for the development of robust EEG biomarkers to detect AD with a clinically acceptable performance by exploiting the combined strengths of key biomarkers. A large number of existing and novel EEG biomarkers associated with slowing of EEG, reduction in EEG complexity and decrease in EEG connectivity were investigated. Support vector machine and linear discriminate analysis methods were used to find the best combination of the EEG biomarkers to detect AD with significant performance. A total of 325,567 EEG biomarkers were investigated, and a panel of six biomarkers was identified and used to create a diagnostic model with high performance (≥85% for sensitivity and 100% for specificity).
用于检测阿尔茨海默病(AD)的生物标志物将使患者能够获得适当的服务,并可能促进新疗法的开发。鉴于受AD影响的人数众多,需要一种低成本、易于使用的方法来检测AD患者。脑电图(EEG)可能在这方面发挥重要作用,但目前尚无单一的EEG生物标志物强大到足以在实际中使用。本研究旨在提供一个方法框架,通过利用关键生物标志物的综合优势,开发出具有临床可接受性能的强大EEG生物标志物以检测AD。研究了大量与EEG减慢、EEG复杂性降低和EEG连通性降低相关的现有和新型EEG生物标志物。使用支持向量机和线性判别分析方法来找到EEG生物标志物的最佳组合,以显著的性能检测AD。共研究了325567个EEG生物标志物,确定了一组六个生物标志物,并用于创建一个高性能的诊断模型(敏感性≥85%,特异性为100%)。