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2
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Alzheimers Dement. 2021 Mar;17(3):327-406. doi: 10.1002/alz.12328. Epub 2021 Mar 23.
3
18F-flortaucipir PET to autopsy comparisons in Alzheimer's disease and other neurodegenerative diseases.18F-氟托西匹 PET 与阿尔茨海默病和其他神经退行性疾病的尸检比较。
Brain. 2020 Dec 5;143(11):3477-3494. doi: 10.1093/brain/awaa276.
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Neuroimaging in Dementia: A Brief Review.痴呆症中的神经影像学:简要综述。
Cureus. 2020 Jun 18;12(6):e8682. doi: 10.7759/cureus.8682.
5
Identification of AV-1451 as a Weak, Nonselective Inhibitor of Monoamine Oxidase.鉴定 AV-1451 为一种弱的、非选择性的单胺氧化酶抑制剂。
ACS Chem Neurosci. 2019 Aug 21;10(8):3839-3846. doi: 10.1021/acschemneuro.9b00326. Epub 2019 Aug 5.
6
F-flortaucipir (AV-1451) tau PET in frontotemporal dementia syndromes.F-氟替卡滨(AV-1451)tau PET 在额颞叶痴呆综合征中的应用。
Alzheimers Res Ther. 2019 Jan 31;11(1):13. doi: 10.1186/s13195-019-0470-7.
7
F-AV-1451 in Parkinson's Disease with and without dementia and in Dementia with Lewy Bodies.F-AV-1451 在帕金森病伴或不伴痴呆及路易体痴呆中的应用。
Sci Rep. 2018 Mar 16;8(1):4717. doi: 10.1038/s41598-018-23041-x.
8
Networks of tau distribution in Alzheimer's disease.阿尔茨海默病中的 tau 分布网络。
Brain. 2018 Feb 1;141(2):568-581. doi: 10.1093/brain/awx353.
9
Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies.废弃术语 FTDP-17,因为 MAPT 突变是散发性额颞叶tau 病的遗传形式。
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10
[F]AV-1451 binding in vivo mirrors the expected distribution of TDP-43 pathology in the semantic variant of primary progressive aphasia.AV-1451 在体内的结合情况反映了 TDP-43 病理学在语义性原发性进行性失语症中的预期分布情况。
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18F-氟替卡匹(AV-1451)在神经退行性疾病诊断中的作用

The Role of 18F-Flortaucipir (AV-1451) in the Diagnosis of Neurodegenerative Disorders.

作者信息

Roy Saswata, Banerjee Dipanjan, Chatterjee Indrajit, Natarajan Deepika, Joy Mathew Christopher

机构信息

General Medicine, Musgrove Park Hospital, Taunton, GBR.

Internal Medicine, East Sussex Healthcare NHS Trust, Hastings, GBR.

出版信息

Cureus. 2021 Jul 26;13(7):e16644. doi: 10.7759/cureus.16644. eCollection 2021 Jul.

DOI:10.7759/cureus.16644
PMID:34458044
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8384382/
Abstract

Tau protein plays a vital role in maintaining the structural and functional integrity of the nervous system; however, hyperphosphorylation or abnormal phosphorylation of tau protein plays an essential role in the pathogenesis of several neurodegenerative disorders. The development of radioligand such as the 18F-flortaucipir (AV-1451) has provided us with the opportunity to assess the underlying tau pathology in various etiologies of dementia. For the purpose of this article, we aimed to evaluate the utility of 18F-AV-1451 in the differential diagnosis of various neurodegenerative disorders. We used PubMed to look for the latest, peer-reviewed, and informative articles. The scope of discussion included the role of 18F-AV-1451 positron emission tomography (PET) to aid in the diagnosis of Alzheimer's disease (AD), frontotemporal dementia (FTD), dementia with Lewy bodies (DLB), and Parkinson's disease with dementia (PDD). We also discussed if the tau burden identified by neuroimaging correlated well with the clinical severity and identified the various challenges of 18F-AV-1451 PET. We concluded that although the role of 18F-AV-1451 seems promising in the neuroimaging of AD, the benefit appears uncertain when it comes to the non-Alzheimer's tauopathies. More research is required to identify the off-target binding sites of 18F-AV-1451 to determine its clinical utility in the future.

摘要

tau蛋白在维持神经系统的结构和功能完整性方面起着至关重要的作用;然而,tau蛋白的过度磷酸化或异常磷酸化在几种神经退行性疾病的发病机制中起着关键作用。放射性配体如18F-氟代托品(AV-1451)的开发为我们提供了评估各种痴呆病因中潜在tau病理的机会。出于本文的目的,我们旨在评估18F-AV-1451在各种神经退行性疾病鉴别诊断中的效用。我们使用PubMed搜索最新的、经过同行评审且内容丰富的文章。讨论范围包括18F-AV-1451正电子发射断层扫描(PET)在辅助诊断阿尔茨海默病(AD)、额颞叶痴呆(FTD)、路易体痴呆(DLB)和帕金森病痴呆(PDD)中的作用。我们还讨论了神经影像学确定的tau负荷是否与临床严重程度密切相关,并确定了18F-AV-1451 PET的各种挑战。我们得出结论,尽管18F-AV-1451在AD的神经影像学中似乎前景广阔,但在非阿尔茨海默病性tau病方面其益处似乎并不确定。需要更多研究来确定18F-AV-1451的脱靶结合位点,以确定其未来的临床效用。