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

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...

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Autores principales: Baloni, Priyanka, Funk, Cory C., Yan, Jingwen, Yurkovich, James T., Kueider-Paisley, Alexandra, Nho, Kwangsik, Heinken, Almut, Jia, Wei, Mahmoudiandehkordi, Siamak, Louie, Gregory, Saykin, Andrew J., Arnold, Matthias, Kastenmüller, Gabi, Griffiths, William J., Thiele, Ines, Kaddurah-Daouk, Rima, Price, Nathan D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691449/
https://www.ncbi.nlm.nih.gov/pubmed/33294859
http://dx.doi.org/10.1016/j.xcrm.2020.100138
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author Baloni, Priyanka
Funk, Cory C.
Yan, Jingwen
Yurkovich, James T.
Kueider-Paisley, Alexandra
Nho, Kwangsik
Heinken, Almut
Jia, Wei
Mahmoudiandehkordi, Siamak
Louie, Gregory
Saykin, Andrew J.
Arnold, Matthias
Kastenmüller, Gabi
Griffiths, William J.
Thiele, Ines
Kaddurah-Daouk, Rima
Price, Nathan D.
author_facet Baloni, Priyanka
Funk, Cory C.
Yan, Jingwen
Yurkovich, James T.
Kueider-Paisley, Alexandra
Nho, Kwangsik
Heinken, Almut
Jia, Wei
Mahmoudiandehkordi, Siamak
Louie, Gregory
Saykin, Andrew J.
Arnold, Matthias
Kastenmüller, Gabi
Griffiths, William J.
Thiele, Ines
Kaddurah-Daouk, Rima
Price, Nathan D.
author_sort Baloni, Priyanka
collection PubMed
description 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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spelling pubmed-76914492020-12-07 Metabolic Network Analysis Reveals Altered Bile Acid Synthesis and Metabolism in Alzheimer’s Disease Baloni, Priyanka Funk, Cory C. Yan, Jingwen Yurkovich, James T. Kueider-Paisley, Alexandra Nho, Kwangsik Heinken, Almut Jia, Wei Mahmoudiandehkordi, Siamak Louie, Gregory Saykin, Andrew J. Arnold, Matthias Kastenmüller, Gabi Griffiths, William J. Thiele, Ines Kaddurah-Daouk, Rima Price, Nathan D. Cell Rep Med Article 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. Elsevier 2020-11-17 /pmc/articles/PMC7691449/ /pubmed/33294859 http://dx.doi.org/10.1016/j.xcrm.2020.100138 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Baloni, Priyanka
Funk, Cory C.
Yan, Jingwen
Yurkovich, James T.
Kueider-Paisley, Alexandra
Nho, Kwangsik
Heinken, Almut
Jia, Wei
Mahmoudiandehkordi, Siamak
Louie, Gregory
Saykin, Andrew J.
Arnold, Matthias
Kastenmüller, Gabi
Griffiths, William J.
Thiele, Ines
Kaddurah-Daouk, Rima
Price, Nathan D.
Metabolic Network Analysis Reveals Altered Bile Acid Synthesis and Metabolism in Alzheimer’s Disease
title Metabolic Network Analysis Reveals Altered Bile Acid Synthesis and Metabolism in Alzheimer’s Disease
title_full Metabolic Network Analysis Reveals Altered Bile Acid Synthesis and Metabolism in Alzheimer’s Disease
title_fullStr Metabolic Network Analysis Reveals Altered Bile Acid Synthesis and Metabolism in Alzheimer’s Disease
title_full_unstemmed Metabolic Network Analysis Reveals Altered Bile Acid Synthesis and Metabolism in Alzheimer’s Disease
title_short Metabolic Network Analysis Reveals Altered Bile Acid Synthesis and Metabolism in Alzheimer’s Disease
title_sort metabolic network analysis reveals altered bile acid synthesis and metabolism in alzheimer’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691449/
https://www.ncbi.nlm.nih.gov/pubmed/33294859
http://dx.doi.org/10.1016/j.xcrm.2020.100138
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