Altered D-glucose in brain parenchyma and cerebrospinal fluid of early Alzheimer's disease detected by dynamic glucose-enhanced MRI

被引:69
作者
Huang, Jianpan [1 ]
van Zijl, Peter C. M. [2 ,3 ]
Han, Xiongqi [1 ]
Dong, Celia M. [4 ]
Cheng, Gerald W. Y. [5 ]
Tse, Kai-Hei [5 ]
Knutsson, Linda [2 ,6 ]
Chen, Lin [2 ,3 ]
Lai, Joseph H. C. [1 ]
Wu, Ed X. [4 ]
Xu, Jiadi [2 ,3 ]
Chan, Kannie W. Y. [1 ,2 ,7 ]
机构
[1] City Univ Hong Kong, Dept Biomed Engn, Hong Kong, Peoples R China
[2] Johns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, Baltimore, MD 21218 USA
[3] Kennedy Krieger Res Inst, FM Kirby Res Ctr Funct Brain Imaging, Baltimore, MD 21205 USA
[4] Univ Hong Kong, Dept Elect & Elect Engn, Hong Kong, Peoples R China
[5] Hong Kong Polytech Univ, Dept Hlth Technol & Informat, Hong Kong, Peoples R China
[6] Lund Univ, Dept Med Radiat Phys, Lund, Sweden
[7] City Univ Hong Kong, Shenzhen Res Inst, Shenzhen, Peoples R China
基金
瑞典研究理事会; 美国国家卫生研究院;
关键词
IN-VIVO; AMYLOID DEPOSITION; MOUSE MODEL; METABOLISM; MICE; TRANSPORT; PET;
D O I
10.1126/sciadv.aba3884
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Altered cerebral glucose uptake is one of the hallmarks of Alzheimer's disease (AD). A dynamic glucose-enhanced (DGE) magnetic resonance imaging (MRI) approach was developed to simultaneously monitor D-glucose uptake and clearance in both brain parenchyma and cerebrospinal fluid (CSF). We observed substantially higher uptake in parenchyma of young (6 months) transgenic AD mice compared to age-matched wild-type (WT) mice. Notably lower uptakes were observed in parenchyma and CSF of old (16 months) AD mice. Both young and old AD mice had an obviously slower CSF clearance than age-matched WT mice. This resembles recent reports of the hampered CSF clearance that leads to protein accumulation in the brain. These findings suggest that DGE MRI can identify altered glucose uptake and clearance in young AD mice upon the emergence of amyloid plaques. DGE MRI of brain parenchyma and CSF has potential for early AD stratification, especially at 3T clinical field strength MRI.
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页数:9
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