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Altered bile acid profile in mild cognitive impairment and Alzheimer's disease: Relationship to neuroimaging and CSF biomarkers.

Alzheimers Dement. 15, 232-244 (2019)
Publishers Version Research data DOI PMC
Open Access Gold (Paid Option)
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as soon as is submitted to ZB.
Introduction: Bile acids (BAs) are the end products of cholesterol metabolism produced by human and gut microbiome co-metabolism. Recent evidence suggests gut microbiota influence pathological features of Alzheimer's disease (AD) including neuroinflammation and amyloid-beta deposition.Method: Serum levels of 20 primary and secondary BA metabolites from the AD Neuroimaging Initiative (n = 1562) were measured using targeted metabolomic profiling. We assessed the association of BAs with the "A/T/N" (amyloid, tau, and neurodegeneration) biomarkers for AD: cerebrospinal fluid (CSF) biomarkers, atrophy (magnetic resonance imaging), and brain glucose metabolism ([F-18]FDG PET).Results: Of 23 BAs and relevant calculated ratios after quality control procedures, three BA signatures were associated with CSFA beta(1-42) ("A") and three with CSF p-tau181 ("T") (corrected P < .05). Furthermore, three, twelve, and fourteen BA signatures were associated with CSF t-tau, glucose metabolism, and atrophy ("N"), respectively (corrected P < .05).Discussion: This is the first study to show serum-based BA metabolites are associated with "A/T/N" AD biomarkers, providing further support for a role of BA pathways in AD pathophysiology. Prospective clinical observations and validation in model systems are needed to assess causality and specific mechanisms underlying this association. (C) 2018 Published by Elsevier Inc. on behalf of the Alzheimer's Association.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Metabolomics ; Bile Acid ; Alzheimer's Disease ; Amyloid-beta ; Csf Biomarkers ; Brain Glucose Metabolism ; Pet ; Mri ; Gut-liver-brain Axis; Isolated Rat Hepatocytes; Surface-based Analysis; Gut-brain Axis; Cerebrospinal-fluid; Cholesterol-metabolism; Ursodeoxycholic Acid; Oxidative Stress; Random-field; Vitamin-d; Fdg-pet
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