Curr Alzheimer Res. 2010 Jun;7(4):334-47. doi: 10.2174/156720510791162412.
The objective was to characterize the non-oscillatory independent components (ICs) of the auditory event-related potential (ERP) waveform of an oddball task for normal and newly diagnosed Alzheimer's disease (AD) subjects, and to seek biomarkers for AD. Single trial ERP waveforms were analysed using independent components analysis (ICA) and k-means clustering. Two stages of clustering depended upon the magnitudes and latencies, and the scalp topographies of the non-oscillatory back-projected ICs (BICs) at electrode Cz. The electrical current dipole sources of the BICs were located using Low Resolution Electromagnetic Tomography (LORETA). Generally 3-10 BICs, of different latencies and polarities, occurred in each trial. Each peak was associated with positive and negative BICs. The trial-to-trial variations in their relative numbers and magnitudes may explain the variations in the averaged ERP reported, and the delay in the averaged P300 for AD patients. The BIC latencies, topographies and electrical current density maximum locations varied from trial-to-trial. Voltage foci in the BIC topographies identify the BIC source locations. Since statistical differences were found between the BICs in healthy and AD subjects, the method might provide reliable biomarkers for AD, if these findings are reproduced in a larger study, independently of other factors influencing the comparison of the two populations. The method can extract artefact- and EEG-free single trial ERP waveforms, offers improved ERP averages by selecting the trials on the basis of their BICs, and is applicable to other evoked potentials, conditions and diseases.
目的是描述正常和新诊断的阿尔茨海默病(AD)受试者的听觉事件相关电位(ERP)波形的非振荡独立成分(IC),并寻找 AD 的生物标志物。使用独立成分分析(ICA)和 K-均值聚类分析对单试 ERP 波形进行分析。两个聚类阶段取决于 Cz 电极处非振荡反向投影 IC(BIC)的幅度和潜伏期以及头皮拓扑结构。使用低分辨率电磁断层成像(LORETA)定位 BIC 的电流偶极子源。通常在每个试验中会出现 3-10 个具有不同潜伏期和极性的 BIC。每个峰都与正 BIC 和负 BIC 相关。它们的相对数量和幅度的试验间变化可能解释了报告的平均 ERP 的变化,以及 AD 患者平均 P300 的延迟。BIC 的潜伏期、拓扑和电流密度最大值位置在试验之间有所不同。BIC 拓扑中的电压焦点确定了 BIC 源的位置。由于在健康和 AD 受试者之间的 BIC 之间发现了统计学差异,如果在更大的研究中独立于影响两种人群比较的其他因素复制这些发现,该方法可能为 AD 提供可靠的生物标志物。该方法可以提取无伪影和 EEG 的单试 ERP 波形,通过根据其 BIC 选择试验来提供改进的 ERP 平均值,并且适用于其他诱发电位、情况和疾病。