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Circulating lipid profiles are associated with cross-sectional and longitudinal changes of central biomarkers for Alzheimer’s disease

Investigating the association of lipidome profiles with central Alzheimer’s disease (AD) biomarkers, including amyloid/tau/neurodegeneration (A/T/N), can provide a holistic view between the lipidome and AD. We performed cross-sectional and longitudinal association analysis of serum lipidome profiles...

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Autores principales: Kim, Jun Pyo, Nho, Kwangsik, Wang, Tingting, Huynh, Kevin, Arnold, Matthias, Risacher, Shannon L., Bice, Paula J., Han, Xianlin, Kristal, Bruce S., Blach, Colette, Baillie, Rebecca, Kastenmüller, Gabi, Meikle, Peter J., Saykin, Andrew J., Kaddurah-Daouk, Rima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312871/
https://www.ncbi.nlm.nih.gov/pubmed/37398438
http://dx.doi.org/10.1101/2023.06.12.23291054
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author Kim, Jun Pyo
Nho, Kwangsik
Wang, Tingting
Huynh, Kevin
Arnold, Matthias
Risacher, Shannon L.
Bice, Paula J.
Han, Xianlin
Kristal, Bruce S.
Blach, Colette
Baillie, Rebecca
Kastenmüller, Gabi
Meikle, Peter J.
Saykin, Andrew J.
Kaddurah-Daouk, Rima
author_facet Kim, Jun Pyo
Nho, Kwangsik
Wang, Tingting
Huynh, Kevin
Arnold, Matthias
Risacher, Shannon L.
Bice, Paula J.
Han, Xianlin
Kristal, Bruce S.
Blach, Colette
Baillie, Rebecca
Kastenmüller, Gabi
Meikle, Peter J.
Saykin, Andrew J.
Kaddurah-Daouk, Rima
author_sort Kim, Jun Pyo
collection PubMed
description Investigating the association of lipidome profiles with central Alzheimer’s disease (AD) biomarkers, including amyloid/tau/neurodegeneration (A/T/N), can provide a holistic view between the lipidome and AD. We performed cross-sectional and longitudinal association analysis of serum lipidome profiles with AD biomarkers in the Alzheimer’s Disease Neuroimaging Initiative cohort (N=1,395). We identified lipid species, classes, and network modules that were significantly associated with cross-sectional and longitudinal changes of A/T/N biomarkers for AD. Notably, we identified the lysoalkylphosphatidylcholine (LPC(O)) as associated with “A/N” biomarkers at baseline at lipid species, class, and module levels. Also, G(M3) ganglioside showed significant association with baseline levels and longitudinal changes of the “N” biomarkers at species and class levels. Our study of circulating lipids and central AD biomarkers enabled identification of lipids that play potential roles in the cascade of AD pathogenesis. Our results suggest dysregulation of lipid metabolic pathways as precursors to AD development and progression.
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spelling pubmed-103128712023-07-01 Circulating lipid profiles are associated with cross-sectional and longitudinal changes of central biomarkers for Alzheimer’s disease Kim, Jun Pyo Nho, Kwangsik Wang, Tingting Huynh, Kevin Arnold, Matthias Risacher, Shannon L. Bice, Paula J. Han, Xianlin Kristal, Bruce S. Blach, Colette Baillie, Rebecca Kastenmüller, Gabi Meikle, Peter J. Saykin, Andrew J. Kaddurah-Daouk, Rima medRxiv Article Investigating the association of lipidome profiles with central Alzheimer’s disease (AD) biomarkers, including amyloid/tau/neurodegeneration (A/T/N), can provide a holistic view between the lipidome and AD. We performed cross-sectional and longitudinal association analysis of serum lipidome profiles with AD biomarkers in the Alzheimer’s Disease Neuroimaging Initiative cohort (N=1,395). We identified lipid species, classes, and network modules that were significantly associated with cross-sectional and longitudinal changes of A/T/N biomarkers for AD. Notably, we identified the lysoalkylphosphatidylcholine (LPC(O)) as associated with “A/N” biomarkers at baseline at lipid species, class, and module levels. Also, G(M3) ganglioside showed significant association with baseline levels and longitudinal changes of the “N” biomarkers at species and class levels. Our study of circulating lipids and central AD biomarkers enabled identification of lipids that play potential roles in the cascade of AD pathogenesis. Our results suggest dysregulation of lipid metabolic pathways as precursors to AD development and progression. Cold Spring Harbor Laboratory 2023-06-21 /pmc/articles/PMC10312871/ /pubmed/37398438 http://dx.doi.org/10.1101/2023.06.12.23291054 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Kim, Jun Pyo
Nho, Kwangsik
Wang, Tingting
Huynh, Kevin
Arnold, Matthias
Risacher, Shannon L.
Bice, Paula J.
Han, Xianlin
Kristal, Bruce S.
Blach, Colette
Baillie, Rebecca
Kastenmüller, Gabi
Meikle, Peter J.
Saykin, Andrew J.
Kaddurah-Daouk, Rima
Circulating lipid profiles are associated with cross-sectional and longitudinal changes of central biomarkers for Alzheimer’s disease
title Circulating lipid profiles are associated with cross-sectional and longitudinal changes of central biomarkers for Alzheimer’s disease
title_full Circulating lipid profiles are associated with cross-sectional and longitudinal changes of central biomarkers for Alzheimer’s disease
title_fullStr Circulating lipid profiles are associated with cross-sectional and longitudinal changes of central biomarkers for Alzheimer’s disease
title_full_unstemmed Circulating lipid profiles are associated with cross-sectional and longitudinal changes of central biomarkers for Alzheimer’s disease
title_short Circulating lipid profiles are associated with cross-sectional and longitudinal changes of central biomarkers for Alzheimer’s disease
title_sort circulating lipid profiles are associated with cross-sectional and longitudinal changes of central biomarkers for alzheimer’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312871/
https://www.ncbi.nlm.nih.gov/pubmed/37398438
http://dx.doi.org/10.1101/2023.06.12.23291054
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