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正电子发射断层扫描(PET)成像检测tau蛋白作为阿尔茨海默病的一种分子检测手段

Tau-PET imaging as a molecular modality for Alzheimer's disease.

作者信息

Ayubcha Cyrus, Rigney Grant, Borja Austin J, Werner Thomas, Alavi Abass

机构信息

Harvard Medical School Boston 02115, MA, USA.

Department of Psychiatry, University of Oxford England OX1 2JD, UK.

出版信息

Am J Nucl Med Mol Imaging. 2021 Oct 15;11(5):374-386. eCollection 2021.

Abstract

Alzheimer's disease (AD) is the most prevalent neurodegenerative condition. The definitive diagnosis of AD remains a post-mortem neuropathological study of the brain. Unfortunately, there are no established diagnostic criteria to achieve an accurate diagnosis of AD in a similarly objective fashion among living patients. Molecular imaging provides one way of enhancing clinical criteria where objective measures of AD correlate to the presence and progression of disease. In this article, the amyloid and tau hypotheses are considered with respect to pathological, imaging, and therapeutic studies. The value of beta-amyloid (Aβ) PET and tau PET are ascertained. Subsequently, the binding characteristics and quality of Aβ and tau tracers are explored. Finally, the value of Aβ and tau imaging in AD can be determined relevant from in-vivo studies of AD patients. Considering the evolving literature in AD and PET imaging, it has become clear that PET can play a role in the diagnosis and prognosis of AD. The use of Aβ imaging has been extensively studied with mixed results suggesting a limited clinical utility. Conversely, tau-PET has shown early success in similar applications as Aβ imaging. Specifically, we find that there is value in FDG-PET and prospective utility in tau-PET. Ultimately, the community must acknowledge that the role of Aβ imaging for diagnosing and managing AD is very limited and that FDG-PET will remain the study of choice at this time. Moreover, research efforts must continue to determine the prospective value of tau imaging to the assessment of this disease.

摘要

阿尔茨海默病(AD)是最常见的神经退行性疾病。AD的确诊仍需对大脑进行尸检神经病理学研究。不幸的是,目前尚无既定的诊断标准能够以类似的客观方式在活体患者中准确诊断AD。分子成像提供了一种增强临床标准的方法,其中AD的客观测量与疾病的存在和进展相关。在本文中,从病理学、影像学和治疗研究方面对淀粉样蛋白和tau蛋白假说进行了探讨。确定了β淀粉样蛋白(Aβ)PET和tau蛋白PET的价值。随后,研究了Aβ和tau蛋白示踪剂的结合特性和质量。最后,根据AD患者的体内研究确定Aβ和tau蛋白成像在AD中的价值。考虑到AD和PET成像领域不断发展的文献,很明显PET可在AD的诊断和预后中发挥作用。对Aβ成像的应用进行了广泛研究,结果不一,表明其临床应用有限。相反,tau蛋白PET在与Aβ成像类似的应用中已初显成效。具体而言,我们发现FDG-PET有价值,tau蛋白PET有潜在应用前景。最终,业界必须认识到Aβ成像在AD诊断和管理中的作用非常有限,目前FDG-PET仍是首选的研究方法。此外,必须继续开展研究工作,以确定tau蛋白成像对该疾病评估的潜在价值。

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本文引用的文献

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An Update on the State of Tau Radiotracer Development: a Brief Review.tau 放射性示踪剂研发现状更新:简要综述。
Mol Imaging Biol. 2021 Dec;23(6):797-808. doi: 10.1007/s11307-021-01612-1. Epub 2021 May 13.
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Mol Neurodegener. 2019 Aug 2;14(1):32. doi: 10.1186/s13024-019-0333-5.

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