The associations between synaptic density and "A/T/N" biomarkers in Alzheimer's disease: An 18F-SynVesT-1 PET/MR study

被引:2
|
作者
Li, Junpeng [1 ,2 ,3 ]
Huang, Qi [1 ,2 ]
Qi, Na [4 ]
He, Kun [1 ,2 ]
Li, Songye [5 ]
Huang, Lin [6 ]
Pan, Fengfeng [6 ]
Ren, Shuhua [1 ,2 ]
Hua, Fengchun [7 ]
Huang, Yiyun [5 ]
Guan, Yihui [1 ,2 ]
Guo, Qihao [6 ]
Zhao, Jun [4 ]
Xie, Fang [1 ,2 ]
机构
[1] Fudan Univ, Huashan Hosp, Dept Nucl Med, Shanghai, Shanghai, Peoples R China
[2] Fudan Univ, Huashan Hosp, PET Ctr, Shanghai, Peoples R China
[3] Soochow Univ, Dept Intens Care Med, Affiliated Hosp 1, Suzhou, Peoples R China
[4] Tongji Univ, Sch Med, Shanghai East Hosp, Dept Nucl Med, Shanghai, Peoples R China
[5] Yale Univ, Sch Med, PET Ctr, Dept Radiol & Biomed Imaging, New Haven, CT 06520 USA
[6] Shanghai Jiao Tong Univ, Peoples Hosp 6, Dept Gerontol, Shanghai, Peoples R China
[7] Shanghai Univ Tradit Chinese Med, Dept Surg Tradit Chinese Med, Longhua Hosp, Shanghai, Peoples R China
来源
基金
美国国家科学基金会; 国家重点研发计划;
关键词
Synaptic vesicle glycoprotein 2A; amyloid-beta deposition; glucose metabolism; cognitive performance; plasma biomarkers; AMYLOID-BETA; GLUCOSE-METABOLISM; TAU DEPOSITION;
D O I
10.1177/0271678X241230733
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A newly developed SV2A radiotracer, F-18-SynVesT-1, was used in this study to investigate synaptic density and its association with Alzheimer's disease (AD) "A/T/N" biomarkers. The study included a cohort of 97 subjects, consisting of 64 patients with cognitive impairment (CI) and 33 individuals with normal cognition (CU). All subjects underwent F-18-SynVesT-1 PET/MR and F-18-florbetapir PET/CT scans. Additionally, a subgroup of individuals also underwent F-18-MK-6240, F-18-FDG PET/CT, plasma A beta 42/A beta 40 and p-tau181 tests. The differences in synaptic density between the groups and the correlations between synaptic density and AD "A/T/N" biomarkers were analyzed. The results showed that compared to the CU group, the CI with A beta+ (CI+) group exhibited the most pronounced synapse loss in the hippocampus, with some loss also observed in the neocortex. Furthermore, synaptic density in the hippocampus and parahippocampal gyrus showed associations with AD biomarkers detected by both imaging and plasma tests in the CI group. The associations between synaptic density and FDG uptake and hippocampal volume were also observed in the CI+ group. In conclusion, the study demonstrated significant synaptic density loss, as measured by the promising tracer F-18-SynVesT-1, and its close correlation with "A/T/N" biomarkers in patients with both Alzheimer's clinical syndrome and pathological changes.
引用
收藏
页码:1199 / 1207
页数:9
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