Herholz Karl
Division of Experimental Psychology and Neuroscience, University of Manchester, Manchester M139PL, UK.
Sheffield Institute for Translational Neuroscience, University of Sheffield, Sheffield S102HQ, UK.
Brain Sci. 2022 Jan 23;12(2):146. doi: 10.3390/brainsci12020146.
Alzheimer's disease (AD) does not present uniform symptoms or a uniform rate of progression in all cases. The classification of subtypes can be based on clinical symptoms or patterns of pathological brain alterations. Imaging techniques may allow for the identification of AD subtypes and their differentiation from other neurodegenerative diseases already at an early stage. In this review, the strengths and weaknesses of current clinical imaging methods are described. These include positron emission tomography (PET) to image cerebral glucose metabolism and pathological amyloid or tau deposits. Magnetic resonance imaging (MRI) is more widely available than PET. It provides information on structural or functional changes in brain networks and their relation to AD subtypes. Amyloid PET provides a very early marker of AD but does not distinguish between AD subtypes. Regional patterns of pathology related to AD subtypes are observed with tau and glucose PET, and eventually as atrophy patterns on MRI. Structural and functional network changes occur early in AD but have not yet provided diagnostic specificity.
阿尔茨海默病(AD)在所有病例中并非都呈现出统一的症状或进展速度。亚型分类可基于临床症状或病理性脑改变模式。成像技术或许能够在早期阶段就识别出AD亚型,并将其与其他神经退行性疾病区分开来。在本综述中,描述了当前临床成像方法的优缺点。这些方法包括用于成像脑葡萄糖代谢以及病理性淀粉样蛋白或tau蛋白沉积的正电子发射断层扫描(PET)。磁共振成像(MRI)比PET更广泛可用。它提供有关脑网络结构或功能变化及其与AD亚型关系的信息。淀粉样蛋白PET提供了AD的一个非常早期的标志物,但无法区分AD亚型。通过tau蛋白和葡萄糖PET可观察到与AD亚型相关的病理学区域模式,最终在MRI上表现为萎缩模式。结构和功能网络变化在AD早期就会出现,但尚未提供诊断特异性。