The gut microbiome in Alzheimer's disease: what we know and what remains to be explored

被引:117
作者
Chandra, Sidhanth [1 ,2 ]
Sisodia, Sangram S. [3 ]
Vassar, Robert J. [1 ]
机构
[1] Northwestern Univ, Ken & Ruth Davee Dept Neurol, Feinberg Sch Med, Chicago, IL 60611 USA
[2] Northwestern Univ, Med Scientist Training Program, Feinberg Sch Med, Chicago, IL 60611 USA
[3] Univ Chicago, Dept Neurobiol, Chicago, IL 60637 USA
关键词
Gut microbiome; Amyloid; Tau; Neuroinflammation; Peripheral immunity; Human; Mouse; Therapeutics; Diet; Sleep; Exercise; HIGH-FAT DIET; MILD COGNITIVE IMPAIRMENT; LONG-TERM POTENTIATION; TRANSGENIC MICE MODEL; MOUSE MODEL; MEDITERRANEAN DIET; A-BETA; AMYLOID HYPOTHESIS; INCIDENT DEMENTIA; INDUCED OBESITY;
D O I
10.1186/s13024-023-00595-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alzheimer's disease (AD), the most common cause of dementia, results in a sustained decline in cognition. There are currently few effective disease modifying therapies for AD, but insights into the mechanisms that mediate the onset and progression of disease may lead to new, effective therapeutic strategies. Amyloid beta oligomers and plaques, tau aggregates, and neuroinflammation play a critical role in neurodegeneration and impact clinical AD progression. The upstream modulators of these pathological features have not been fully clarified, but recent evidence indicates that the gut microbiome (GMB) may have an influence on these features and therefore may influence AD progression in human patients. In this review, we summarize studies that have identified alterations in the GMB that correlate with pathophysiology in AD patients and AD mouse models. Additionally, we discuss findings with GMB manipulations in AD models and potential GMB-targeted therapeutics for AD. Lastly, we discuss diet, sleep, and exercise as potential modifiers of the relationship between the GMB and AD and conclude with future directions and recommendations for further studies of this topic.
引用
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页数:21
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