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Inflammation and the pathological progression of Alzheimer’s disease are associated with low circulating choline levels

Deficiency of dietary choline, an essential nutrient, is observed worldwide, with ~ 90% of Americans being deficient. Previous work highlights a relationship between decreased choline intake and an increased risk for cognitive decline and Alzheimer’s disease (AD). The associations between blood circ...

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Autores principales: Judd, Jessica M., Jasbi, Paniz, Winslow, Wendy, Serrano, Geidy E., Beach, Thomas G., Klein-Seetharaman, Judith, Velazquez, Ramon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499952/
https://www.ncbi.nlm.nih.gov/pubmed/37548694
http://dx.doi.org/10.1007/s00401-023-02616-7
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author Judd, Jessica M.
Jasbi, Paniz
Winslow, Wendy
Serrano, Geidy E.
Beach, Thomas G.
Klein-Seetharaman, Judith
Velazquez, Ramon
author_facet Judd, Jessica M.
Jasbi, Paniz
Winslow, Wendy
Serrano, Geidy E.
Beach, Thomas G.
Klein-Seetharaman, Judith
Velazquez, Ramon
author_sort Judd, Jessica M.
collection PubMed
description Deficiency of dietary choline, an essential nutrient, is observed worldwide, with ~ 90% of Americans being deficient. Previous work highlights a relationship between decreased choline intake and an increased risk for cognitive decline and Alzheimer’s disease (AD). The associations between blood circulating choline and the pathological progression in both mild cognitive impairment (MCI) and AD remain unknown. Here, we examined these associations in a cohort of patients with MCI with presence of either sparse or high neuritic plaque density and Braak stage and a second cohort with either moderate AD (moderate to frequent neuritic plaques, Braak stage = IV) or severe AD (frequent neuritic plaques, Braak stage = VI), compared to age-matched controls. Metabolomic analysis was performed on serum from the AD cohort. We then assessed the effects of dietary choline deficiency (Ch−) in 3xTg-AD mice and choline supplementation (Ch+) in APP/PS1 mice, two rodent models of AD. The levels of circulating choline were reduced while pro-inflammatory cytokine TNFα was elevated in serum of both MCI sparse and high pathology cases. Reduced choline and elevated TNFα correlated with higher neuritic plaque density and Braak stage. In AD patients, we found reductions in choline, its derivative acetylcholine (ACh), and elevated TNFα. Choline and ACh levels were negatively correlated with neuritic plaque load, Braak stage, and TNFα, but positively correlated with MMSE, and brain weight. Metabolites L-Valine, 4-Hydroxyphenylpyruvic, Methylmalonic, and Ferulic acids were significantly associated with circuiting choline levels. In 3xTg-AD mice, the Ch− diet increased amyloid-β levels and tau phosphorylation in cortical tissue, and TNFα in both blood and cortical tissue, paralleling the severe human-AD profile. Conversely, the Ch+ diet increased choline and ACh while reducing amyloid-β and TNFα levels in brains of APP/PS1 mice. Collectively, low circulating choline is associated with AD-neuropathological progression, illustrating the importance of adequate dietary choline intake to offset disease. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00401-023-02616-7.
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spelling pubmed-104999522023-09-15 Inflammation and the pathological progression of Alzheimer’s disease are associated with low circulating choline levels Judd, Jessica M. Jasbi, Paniz Winslow, Wendy Serrano, Geidy E. Beach, Thomas G. Klein-Seetharaman, Judith Velazquez, Ramon Acta Neuropathol Original Paper Deficiency of dietary choline, an essential nutrient, is observed worldwide, with ~ 90% of Americans being deficient. Previous work highlights a relationship between decreased choline intake and an increased risk for cognitive decline and Alzheimer’s disease (AD). The associations between blood circulating choline and the pathological progression in both mild cognitive impairment (MCI) and AD remain unknown. Here, we examined these associations in a cohort of patients with MCI with presence of either sparse or high neuritic plaque density and Braak stage and a second cohort with either moderate AD (moderate to frequent neuritic plaques, Braak stage = IV) or severe AD (frequent neuritic plaques, Braak stage = VI), compared to age-matched controls. Metabolomic analysis was performed on serum from the AD cohort. We then assessed the effects of dietary choline deficiency (Ch−) in 3xTg-AD mice and choline supplementation (Ch+) in APP/PS1 mice, two rodent models of AD. The levels of circulating choline were reduced while pro-inflammatory cytokine TNFα was elevated in serum of both MCI sparse and high pathology cases. Reduced choline and elevated TNFα correlated with higher neuritic plaque density and Braak stage. In AD patients, we found reductions in choline, its derivative acetylcholine (ACh), and elevated TNFα. Choline and ACh levels were negatively correlated with neuritic plaque load, Braak stage, and TNFα, but positively correlated with MMSE, and brain weight. Metabolites L-Valine, 4-Hydroxyphenylpyruvic, Methylmalonic, and Ferulic acids were significantly associated with circuiting choline levels. In 3xTg-AD mice, the Ch− diet increased amyloid-β levels and tau phosphorylation in cortical tissue, and TNFα in both blood and cortical tissue, paralleling the severe human-AD profile. Conversely, the Ch+ diet increased choline and ACh while reducing amyloid-β and TNFα levels in brains of APP/PS1 mice. Collectively, low circulating choline is associated with AD-neuropathological progression, illustrating the importance of adequate dietary choline intake to offset disease. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00401-023-02616-7. Springer Berlin Heidelberg 2023-08-07 2023 /pmc/articles/PMC10499952/ /pubmed/37548694 http://dx.doi.org/10.1007/s00401-023-02616-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Paper
Judd, Jessica M.
Jasbi, Paniz
Winslow, Wendy
Serrano, Geidy E.
Beach, Thomas G.
Klein-Seetharaman, Judith
Velazquez, Ramon
Inflammation and the pathological progression of Alzheimer’s disease are associated with low circulating choline levels
title Inflammation and the pathological progression of Alzheimer’s disease are associated with low circulating choline levels
title_full Inflammation and the pathological progression of Alzheimer’s disease are associated with low circulating choline levels
title_fullStr Inflammation and the pathological progression of Alzheimer’s disease are associated with low circulating choline levels
title_full_unstemmed Inflammation and the pathological progression of Alzheimer’s disease are associated with low circulating choline levels
title_short Inflammation and the pathological progression of Alzheimer’s disease are associated with low circulating choline levels
title_sort inflammation and the pathological progression of alzheimer’s disease are associated with low circulating choline levels
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499952/
https://www.ncbi.nlm.nih.gov/pubmed/37548694
http://dx.doi.org/10.1007/s00401-023-02616-7
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