An integrated neuroimaging-omics approach for the gut-brain communication pathways in Alzheimer's disease

被引:5
作者
Sheng, Can [1 ]
Du, Wenying [2 ]
Liang, Yuan [1 ]
Xu, Peng [1 ]
Ding, Qingqing [1 ]
Chen, Xue [1 ]
Jia, Shulei [3 ]
Wang, Xiaoni [4 ]
机构
[1] Jining Med Univ, Dept Neurol, Affiliated Hosp, Jining, Peoples R China
[2] China Japan Friendship Hosp, Dept Neurol, Beijing, Peoples R China
[3] Chinese Acad Sci, Inst Microbiol, Beijing, Peoples R China
[4] Zhejiang Univ, Sir Run Run Shaw Hosp, Sch Med, Dept Neurol, Hangzhou, Peoples R China
来源
FRONTIERS IN AGING NEUROSCIENCE | 2023年 / 15卷
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; microbiome; metabolome; neuroimaging; microbiota-gut-brain axis; CHAIN FATTY-ACIDS; MICROBIOTA; INHIBITION; METABOLISM; MARKERS; AXIS;
D O I
10.3389/fnagi.2023.1211979
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
A key role of the gut microbiota in the pathogenesis of neurodegenerative diseases, such as Alzheimer's disease (AD), has been identified over the past decades. Increasing clinical and preclinical evidence implicates that there is bidirectional communication between the gut microbiota and the central nervous system (CNS), which is also known as the microbiota-gut-brain axis. Nevertheless, current knowledge on the interplay between gut microbiota and the brain remains largely unclear. One of the primary mediating factors by which the gut microbiota interacts with the host is peripheral metabolites, including blood or gut-derived metabolites. However, mechanistic knowledge about the effect of the microbiome and metabolome signaling on the brain is limited. Neuroimaging techniques, such as multi-modal magnetic resonance imaging (MRI), and fluorodeoxyglucose-positron emission tomography (FDG-PET), have the potential to directly elucidate brain structural and functional changes corresponding with alterations of the gut microbiota and peripheral metabolites in vivo. Employing a combination of gut microbiota, metabolome, and advanced neuroimaging techniques provides a future perspective in illustrating the microbiota-gut-brain pathway and further unveiling potential therapeutic targets for AD treatments.
引用
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页数:7
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