4.6 Article

Metabolic Network Analysis Reveals Altered Bile Acid Synthesis and Metabolism in Alzheimer's Disease

期刊

CELL REPORTS MEDICINE
卷 1, 期 8, 页码 -

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CELL PRESS
DOI: 10.1016/j.xcrm.2020.100138

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资金

  1. AMP-AD Consortium
  2. National Institute on Aging (NIA), a component of the Accelerated Medicines Partnership for AD (AMP-AD) Target Discovery and Preclinical Validation Project [R01AG046171]
  3. NIA, a component of the M2OVE-AD Consortium (Molecular Mechanisms of the Vascular Etiology of AD-Consortium [RF1 AG0151550]
  4. NIA grant [P30AG10161, R01AG15819, R01AG17917, U01AG46152, RF1 AG058942, R01 AG057452, NLMR01 LM012535, NIA R03 AG054936]
  5. Qatar National Research Fund [NPRP8-061-3-011]
  6. NIH [P30 AG010133, R01 AG019771, R01 CA129769]
  7. UK Biotechnology and Biological Sciences Research Council [BB/I001735/1, BB/N015932/1]
  8. Engineering and Physical Sciences Research Council via an Impact Acceleration Account
  9. Institute for Systems Biology's Translational Research Fellows Program
  10. BBSRC [BB/N015932/1, BB/I001735/1] Funding Source: UKRI

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Increasing evidence suggests Alzheimer's disease (AD) pathophysiology is influenced by primary and secondary bile acids, the end product of cholesterol metabolism. We analyze 2,114 post-mortem brain transcriptomes and identify genes in the alternative bile acid synthesis pathway to be expressed in the brain. A targeted metabolomic analysis of primary and secondary bile acids measured from post-mortem brain samples of 111 individuals supports these results. Our metabolic network analysis suggests that taurine transport, bile acid synthesis, and cholesterol metabolism differ in AD and cognitively normal individuals. We also identify putative transcription factors regulating metabolic genes and influencing altered metabolism in AD. Intriguingly, some bile acids measured in brain tissue cannot be explained by the presence of enzymes responsible for their synthesis, suggesting that they may originate from the gut microbiome and are transported to the brain. These findings motivate further research into bile acid metabolism in AD to elucidate their possible connection to cognitive decline.

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