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淀粉样蛋白和 Tau 蛋白正电子发射断层扫描成像在阿尔茨海默病及其他 Tau 蛋白病中的应用

Amyloid and Tau Positron Emission Tomography Imaging in Alzheimer's Disease and Other Tauopathies.

作者信息

Maschio Cinzia, Ni Ruiqing

机构信息

Institute for Regenerative Medicine, University of Zurich, Zurich, Switzerland.

Institute for Biomedical Engineering, ETH Zürich and University of Zurich, Zurich, Switzerland.

出版信息

Front Aging Neurosci. 2022 Apr 22;14:838034. doi: 10.3389/fnagi.2022.838034. eCollection 2022.

Abstract

The detection and staging of Alzheimer's disease (AD) using non-invasive imaging biomarkers is of substantial clinical importance. Positron emission tomography (PET) provides readouts to uncover molecular alterations in the brains of AD patients with high sensitivity and specificity. A variety of amyloid-β (Aβ) and tau PET tracers are already available for the clinical diagnosis of AD, but there is still a lack of imaging biomarkers with high affinity and selectivity for tau inclusions in primary tauopathies, such as progressive supranuclear palsy (PSP), corticobasal degeneration (CBD) and Pick's disease (PiD). This review aims to provide an overview of the existing Aβ and tau PET imaging biomarkers and their binding properties from , , and assessment. Imaging biomarkers for pathologic proteins are vital for clinical diagnosis, disease staging and monitoring of the potential therapeutic approaches of AD. Off-target binding of radiolabeled tracers to white matter or other neural structures is one confounding factor when interpreting images. To improve binding properties such as binding affinity and to eliminate off-target binding, second generation of tau PET tracers have been developed. To conclude, we further provide an outlook for imaging tauopathies and other pathological features of AD and primary tauopathies.

摘要

使用非侵入性成像生物标志物对阿尔茨海默病(AD)进行检测和分期具有重大临床意义。正电子发射断层扫描(PET)能够提供读数,以高灵敏度和特异性揭示AD患者大脑中的分子变化。多种淀粉样β蛋白(Aβ)和tau蛋白PET示踪剂已用于AD的临床诊断,但在原发性tau蛋白病,如进行性核上性麻痹(PSP)、皮质基底节变性(CBD)和Pick病(PiD)中,仍缺乏对tau蛋白包涵体具有高亲和力和选择性的成像生物标志物。本综述旨在概述现有的Aβ和tau蛋白PET成像生物标志物及其从、和评估得出的结合特性。病理性蛋白的成像生物标志物对于AD的临床诊断、疾病分期以及潜在治疗方法的监测至关重要。在解读图像时,放射性标记示踪剂与白质或其他神经结构的非靶向结合是一个混杂因素。为了改善诸如结合亲和力等结合特性并消除非靶向结合,已开发出第二代tau蛋白PET示踪剂。总之,我们进一步展望了tau蛋白病以及AD和原发性tau蛋白病的其他病理特征的成像前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8df6/9074832/fd47b32930de/fnagi-14-838034-g001.jpg

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