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MahmoudianDehkordi, S.* ; Arnold, M. ; Nho, K.* ; Ahmad, S.* ; Jia, W.* ; Xie, G.* ; Louie, G.* ; Kueider-Paisley, A.* ; Moseley, M.A.* ; Thompson, J.W.* ; St John Williams, L.* ; Tenenbaum, J.D.* ; Blach, C.* ; Baillie, R.A.* ; Han, X.* ; Bhattacharyya, S.* ; Toledo, J.B.* ; Schafferer, S.* ; Klein, S.* ; Koal, T.* ; Risacher, S.L.* ; Kling, M.A.* ; Motsinger-Reif, A.* ; Rotroff, D.M.* ; Jack, J.R.* ; Hankemeier, T.* ; Bennett, D.A.* ; de Jager, P.L.* ; Trojanowski, J.Q.* ; Shaw, L.M.* ; Weiner, M.W.* ; Doraiswamy, P.M.* ; van Duijn, C.M.* ; Saykin, A.J.* ; Kastenmüller, G. ; Kaddurah-Daouk, R.*

Altered bile acid profile associates with cognitive impairment in Alzheimer's disease-An emerging role for gut microbiome.

Alzheimers Dement. 15, 76-92 (2018)
Verlagsversion Postprint Forschungsdaten DOI PMC
Open Access Gold (Paid Option)
Creative Commons Lizenzvertrag
Introduction: Increasing evidence suggests a role for the gut microbiome in central nervous system disorders and a specific role for the gut-brain axis in neurodegeneration. Bile acids (BAs), products of cholesterol metabolism and clearance, are produced in the liver and are further metabolized by gut bacteria. They have major regulatory and signaling functions and seem dysregulated in Alzheimer's disease (AD).Methods: Serum levels of 15 primary and secondary BAs and their conjugated forms were measured in 1464 subjects including 370 cognitively normal older adults, 284 with early mild cognitive impairment, 505 with late mild cognitive impairment, and 305 AD cases enrolled in the AD Neuroimaging Initiative. We assessed associations of BA profiles including selected ratios with diagnosis, cognition, and AD-related genetic variants, adjusting for confounders and multiple testing.Results: In AD compared to cognitively normal older adults, we observed significantly lower serum concentrations of a primary BA (cholic acid [CA]) and increased levels of the bacterially produced, secondary BA, deoxycholic acid, and its glycine and taurine conjugated forms. An increased ratio of deoxycholic acid: CA, which reflects 7 alpha-dehydroxylation of CA by gut bacteria, strongly associated with cognitive decline, a finding replicated in serum and brain samples in the Rush Religious Orders and Memory and Aging Project. Several genetic variants in immune response-related genes implicated in AD showed associations with BA profiles.Discussion: We report for the first time an association between altered BA profile, genetic variants implicated in AD, and cognitive changes in disease using a large multicenter study. These findings warrant further investigation of gut dysbiosis and possible role of gut-liver-brain axis in the pathogenesis of AD. (C) 2018 The Authors. Published by Elsevier Inc. on behalf of the Alzheimer's Association.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Metabolomics ; Metabolome ; Lipidomics ; Alzheimer's Disease ; Gut Microbiome ; Gut-liver-brain Axis ; Atlas For Alzheimer ; Genetic Variants ; Immunity ; Inflammation; Ursodeoxycholic Acid; Brain-development; Rat Hepatocytes; Blood; Apoptosis; Pathology; Variants; Mice; Neuroinflammation; Progression
ISSN (print) / ISBN 1552-5260
e-ISSN 1552-5279
Zeitschrift Alzheimer's & Dementia
Quellenangaben Band: 15, Heft: 1, Seiten: 76-92 Artikelnummer: , Supplement: ,
Verlag Elsevier
Verlagsort New York, NY [u.a.]
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Computational Biology (ICB)
Institute of Bioinformatics and Systems Biology (IBIS)