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

Sidhanth Chandra, Sangram S. Sisodia, Robert J. Vassar*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

91 Scopus citations

Abstract

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.

Original languageEnglish (US)
Article number9
JournalMolecular neurodegeneration
Volume18
Issue number1
DOIs
StatePublished - Dec 2023

Funding

Our source of funding for this project was from Open Philanthropy and the Good Ventures Foundation (to R. Vassar, S. Sisodia). This funding was the primary funding mechanism for the study. S Chandra was supported by F30AG079577 (to S Chandra) and NIGMS T32GM008152 (to Northwestern University Medical Scientist Training Program).

Keywords

  • Amyloid
  • Diet
  • Exercise
  • Gut microbiome
  • Human
  • Mouse
  • Neuroinflammation
  • Peripheral immunity
  • Sleep
  • Tau
  • Therapeutics

ASJC Scopus subject areas

  • Clinical Neurology
  • Cellular and Molecular Neuroscience
  • Molecular Biology

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