认知功能障碍受试者血浆和PET成像ATN标记物的头对头比较。

IF 10.8 1区 医学 Q1 NEUROSCIENCES Translational Neurodegeneration Pub Date : 2023-06-29 DOI:10.1186/s40035-023-00365-x
Jiaying Lu, Xiaoxi Ma, Huiwei Zhang, Zhenxu Xiao, Ming Li, Jie Wu, Zizhao Ju, Li Chen, Li Zheng, Jingjie Ge, Xiaoniu Liang, Weiqi Bao, Ping Wu, Ding Ding, Tzu-Chen Yen, Yihui Guan, Chuantao Zuo, Qianhua Zhao
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引用次数: 0

摘要

背景:获得更多关于阿尔茨海默病(AD)谱系中ATN(淀粉样蛋白/Tau/神经变性)框架内不同生物标志物之间相互关联的信息具有临床相关性。我们旨在对有认知障碍的受试者的血浆和正电子发射断层扫描(PET)ATN生物标志物进行全面的头对头比较。方法:以医院为基础的一组患有认知功能障碍并同时进行抽血和ATN PET成像的受试者(18F-氟倍他匹用于A,18F-氟唑他用于T,18F-脱氧葡萄糖[18F-FDG]用于N)被纳入研究(N = 137)。β-淀粉样蛋白(Aβ)状态(阳性与阴性)和认知障碍的严重程度是评估生物标志物性能的主要结果指标。结果:在整个队列中,发现血浆磷酸化tau181(p-tau181)水平与ATN生物标志物的PET成像有关。AT生物标志物的血浆p-tau181水平和PET标准化摄取值比率在区分aβ+ 和Aβ受试者。在Aβ+受试者中,tau负荷增加和葡萄糖代谢低下与认知障碍的严重程度显著相关。此外,在Aβ受试者中,葡萄糖代谢低下以及血浆神经丝轻链水平升高与更严重的认知障碍有关。结论:血浆p-tau181、18F-florbetapir和18F-Florzolotau PET显像可作为评估AD症状期Aβ状态的可互换生物标志物。18F-Florzootau和18F-FDG PET显像可用于评估认知障碍的严重程度。我们的发现对确定最适合临床使用的ATN生物标志物的路线图具有启示意义。
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Head-to-head comparison of plasma and PET imaging ATN markers in subjects with cognitive complaints.

Background: Gaining more information about the reciprocal associations between different biomarkers within the ATN (Amyloid/Tau/Neurodegeneration) framework across the Alzheimer's disease (AD) spectrum is clinically relevant. We aimed to conduct a comprehensive head-to-head comparison of plasma and positron emission tomography (PET) ATN biomarkers in subjects with cognitive complaints.

Methods: A hospital-based cohort of subjects with cognitive complaints with a concurrent blood draw and ATN PET imaging (18F-florbetapir for A, 18F-Florzolotau for T, and 18F-fluorodeoxyglucose [18F-FDG] for N) was enrolled (n = 137). The β-amyloid (Aβ) status (positive versus negative) and the severity of cognitive impairment served as the main outcome measures for assessing biomarker performances.

Results: Plasma phosphorylated tau 181 (p-tau181) level was found to be associated with PET imaging of ATN biomarkers in the entire cohort. Plasma p-tau181 level and PET standardized uptake value ratios of AT biomarkers showed a similarly excellent diagnostic performance for distinguishing between Aβ+ and Aβ- subjects. An increased tau burden and glucose hypometabolism were significantly associated with the severity of cognitive impairment in Aβ+ subjects. Additionally, glucose hypometabolism - along with elevated plasma neurofilament light chain level - was related to more severe cognitive impairment in Aβ- subjects.

Conclusion: Plasma p-tau181, as well as 18F-florbetapir and 18F-Florzolotau PET imaging can be considered as interchangeable biomarkers in the assessment of Aβ status in symptomatic stages of AD. 18F-Florzolotau and 18F-FDG PET imaging could serve as biomarkers for the severity of cognitive impairment. Our findings have implications for establishing a roadmap to identifying the most suitable ATN biomarkers for clinical use.

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来源期刊
Translational Neurodegeneration
Translational Neurodegeneration Neuroscience-Cognitive Neuroscience
CiteScore
19.50
自引率
0.80%
发文量
44
审稿时长
10 weeks
期刊介绍: Translational Neurodegeneration, an open-access, peer-reviewed journal, addresses all aspects of neurodegenerative diseases. It serves as a prominent platform for research, therapeutics, and education, fostering discussions and insights across basic, translational, and clinical research domains. Covering Parkinson's disease, Alzheimer's disease, and other neurodegenerative conditions, it welcomes contributions on epidemiology, pathogenesis, diagnosis, prevention, drug development, rehabilitation, and drug delivery. Scientists, clinicians, and physician-scientists are encouraged to share their work in this specialized journal tailored to their fields.
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