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一篇关于用于tau神经原纤维缠结正电子发射断层扫描成像的氟替卡匹文献综述。

A review of the flortaucipir literature for positron emission tomography imaging of tau neurofibrillary tangles.

作者信息

Burnham Samantha C, Iaccarino Leonardo, Pontecorvo Michael J, Fleisher Adam S, Lu Ming, Collins Emily C, Devous Michael D

机构信息

Avid, Eli Lilly and Company, Philadelphia, PA 19104, USA.

出版信息

Brain Commun. 2023 Nov 16;6(1):fcad305. doi: 10.1093/braincomms/fcad305. eCollection 2024.


DOI:10.1093/braincomms/fcad305
PMID:38187878
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10768888/
Abstract

Alzheimer's disease is defined by the presence of β-amyloid plaques and neurofibrillary tau tangles potentially preceding clinical symptoms by many years. Previously only detectable post-mortem, these pathological hallmarks are now identifiable using biomarkers, permitting an definitive diagnosis of Alzheimer's disease. F-flortaucipir (previously known as F-T807; F-AV-1451) was the first tau positron emission tomography tracer to be introduced and is the only Food and Drug Administration-approved tau positron emission tomography tracer (Tauvid™). It has been widely adopted and validated in a number of independent research and clinical settings. In this review, we present an overview of the published literature on flortaucipir for positron emission tomography imaging of neurofibrillary tau tangles. We considered all accessible peer-reviewed literature pertaining to flortaucipir through 30 April 2022. We found 474 relevant peer-reviewed publications, which were organized into the following categories based on their primary focus: typical Alzheimer's disease, mild cognitive impairment and pre-symptomatic populations; atypical Alzheimer's disease; non-Alzheimer's disease neurodegenerative conditions; head-to-head comparisons with other Tau positron emission tomography tracers; and technical considerations. The available flortaucipir literature provides substantial evidence for the use of this positron emission tomography tracer in assessing neurofibrillary tau tangles in Alzheimer's disease and limited support for its use in other neurodegenerative disorders. Visual interpretation and quantitation approaches, although heterogeneous, mostly converge and demonstrate the high diagnostic and prognostic value of flortaucipir in Alzheimer's disease.

摘要

阿尔茨海默病的定义是存在β-淀粉样蛋白斑块和神经原纤维缠结,这些病理特征可能在临床症状出现前数年就已存在。以前这些病理特征只能在尸检时检测到,现在可以使用生物标志物进行识别,从而能够对阿尔茨海默病进行明确诊断。F-氟代托品(以前称为F-T807;F-AV-1451)是首个被引入的tau正电子发射断层扫描示踪剂,也是唯一获得美国食品药品监督管理局批准的tau正电子发射断层扫描示踪剂(Tauvid™)。它已在许多独立的研究和临床环境中得到广泛应用和验证。在本综述中,我们概述了已发表的关于氟代托品用于神经原纤维缠结正电子发射断层扫描成像的文献。我们检索了截至2022年4月30日所有可获取的与氟代托品相关的同行评审文献。我们发现了474篇相关的同行评审出版物,并根据其主要重点分为以下几类:典型阿尔茨海默病、轻度认知障碍和症状前人群;非典型阿尔茨海默病;非阿尔茨海默病神经退行性疾病;与其他tau正电子发射断层扫描示踪剂的头对头比较;以及技术考量。现有的氟代托品文献为使用这种正电子发射断层扫描示踪剂评估阿尔茨海默病中的神经原纤维缠结提供了大量证据,而对其在其他神经退行性疾病中的应用支持有限。视觉解读和定量方法虽然各不相同,但大多趋于一致,并证明了氟代托品在阿尔茨海默病中的高诊断和预后价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71f/10768888/7c510881aaf7/fcad305_ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71f/10768888/7c510881aaf7/fcad305_ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71f/10768888/7c510881aaf7/fcad305_ga1.jpg

相似文献

[1]
A review of the flortaucipir literature for positron emission tomography imaging of tau neurofibrillary tangles.

Brain Commun. 2023-11-16

[2]
18F-flortaucipir PET to autopsy comparisons in Alzheimer's disease and other neurodegenerative diseases.

Brain. 2020-12-5

[3]
Relationships between flortaucipir PET tau binding and amyloid burden, clinical diagnosis, age and cognition.

Brain. 2017-3-1

[4]
β-Amyloid discordance of cerebrospinal fluid and positron emission tomography imaging shows distinct spatial tau patterns.

Brain Commun. 2022-3-31

[5]
Test-Retest Reproducibility for the Tau PET Imaging Agent Flortaucipir F 18.

J Nucl Med. 2017-12-28

[6]
Tauvid™: The First FDA-Approved PET Tracer for Imaging Tau Pathology in Alzheimer's Disease.

Pharmaceuticals (Basel). 2021-1-30

[7]
The Sensitivity of Tau Tracers for the Discrimination of Alzheimer's Disease Patients and Healthy Controls by PET.

Biomolecules. 2023-2-3

[8]
Longitudinal 18F-MK-6240 tau tangles accumulation follows Braak stages.

Brain. 2021-12-16

[9]
Regional profiles of the candidate tau PET ligand 18F-AV-1451 recapitulate key features of Braak histopathological stages.

Brain. 2016-3-2

[10]
Associations between quantitative [F]flortaucipir tau PET and atrophy across the Alzheimer's disease spectrum.

Alzheimers Res Ther. 2019-7-4

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Cells. 2025-7-18

[2]
Return of research results across the Alzheimer's Disease Research Centers network.

Alzheimers Dement. 2025-6

[3]
Revisiting the therapeutic landscape of tauopathies: assessing the current pipeline and clinical trials.

Alzheimers Res Ther. 2025-6-4

[4]
Modeling functional connectivity with learning and memory in a mouse model of Alzheimer's disease.

Front Neuroimaging. 2025-4-25

[5]
Targeting Tau Protein with Proximity Inducing Modulators: A New Frontier to Combat Tauopathies.

ACS Pharmacol Transl Sci. 2025-2-10

[6]
Genomic and Transcriptomic Approaches Advance the Diagnosis and Prognosis of Neurodegenerative Diseases.

Genes (Basel). 2025-1-24

[7]
A multi-cohort study of longitudinal and cross-sectional Alzheimer's disease biomarkers in cognitively unimpaired older adults.

Alzheimers Dement. 2025-2

[8]
Clinical use of biomarkers in the era of Alzheimer's disease treatments.

Alzheimers Dement. 2025-1

本文引用的文献

[1]
A fluid biomarker accurately detects tau aggregate pathology in Alzheimer's disease.

Nat Med. 2023-8

[2]
Donanemab in Early Symptomatic Alzheimer Disease: The TRAILBLAZER-ALZ 2 Randomized Clinical Trial.

JAMA. 2023-8-8

[3]
Designing the next-generation clinical care pathway for Alzheimer's disease.

Nat Aging. 2022-8

[4]
Association of Amyloid Reduction After Donanemab Treatment With Tau Pathology and Clinical Outcomes: The TRAILBLAZER-ALZ Randomized Clinical Trial.

JAMA Neurol. 2022-10-1

[5]
Optimum Differentiation of Frontotemporal Lobar Degeneration from Alzheimer Disease Achieved with Cross-Sectional Tau Positron Emission Tomography.

Ann Neurol. 2022-12

[6]
Altered excitatory and inhibitory neuronal subpopulation parameters are distinctly associated with tau and amyloid in Alzheimer's disease.

Elife. 2022-5-26

[7]
Monoamine oxidase binding not expected to significantly affect [F]flortaucipir PET interpretation.

Eur J Nucl Med Mol Imaging. 2022-9

[8]
Season of birth and vulnerability to the pathology of Alzheimer's disease: an in vivo positron emission tomography study.

Psychogeriatrics. 2022-7

[9]
Rates of β-amyloid deposition indicate widespread simultaneous accumulation throughout the brain.

Neurobiol Aging. 2022-7

[10]
Regional Aβ-tau interactions promote onset and acceleration of Alzheimer's disease tau spreading.

Neuron. 2022-6-15

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