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UNIQUE TRANSKINGDOM MICROBIOME SIGNATURES LINKED WITH COGNITIVE DECLINE IN OLDER ADULTS OF MIAGB CONSORTIUM COHORT

The prevalence of age-related cognitive disorders is increasing. Effective prevention and treatment interventions are unavailable due to a poor understanding of aging biology. Multiple emerging evidence indicates that the gut microbiome is linked with age-related disorders; however, their clinical i...

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Autores principales: Chaudhari, Diptaraj, Jain, Shalini, Yadav, Hariom, Masternak, Michal, Holland, Peter, Agronin, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9766942/
http://dx.doi.org/10.1093/geroni/igac059.2781
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author Chaudhari, Diptaraj
Jain, Shalini
Yadav, Hariom
Masternak, Michal
Holland, Peter
Agronin, Marc
author_facet Chaudhari, Diptaraj
Jain, Shalini
Yadav, Hariom
Masternak, Michal
Holland, Peter
Agronin, Marc
author_sort Chaudhari, Diptaraj
collection PubMed
description The prevalence of age-related cognitive disorders is increasing. Effective prevention and treatment interventions are unavailable due to a poor understanding of aging biology. Multiple emerging evidence indicates that the gut microbiome is linked with age-related disorders; however, their clinical importance in differentiating and predicting the risk of cognitive decline or dementia is largely elusive. Utilizing samples and data of a large, multi-site clinical study across the state of Florida called Microbiome in aging Gut and Brain (MiaGB) Consortium, our whole genome microbiome sequencing revealed that the viral and archaeal population was significantly reduced in the gut of older adults with dementia (n=8) compared to those with mild cognitive impairment (MCI) (n=25) and normal cognition (n=59). Whereas the fungi were exclusively detected in the controls only. Alpha diversity of the participants with MCI and dementia was lower than the cognitively healthy controls. The abundance of Actinobacteria and Verrucomicrobia phyla was higher, and Firmicutes phylum was lower in the participants with dementia. Bacteriophages Lactobacillus prophage Lj771 and Microbacterium phage Min1 were exclusively detected in the gut of the participants with dementia. The study also identifies key metabolic pathways altered in the controls versus the cognitive impairment state. Our biomarker discovery analyses also revealed that these unique microbiome signatures and pathways might have predictive power for cognitive decline and dementia risk and offer new targets for future therapeutic interventions.
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spelling pubmed-97669422022-12-21 UNIQUE TRANSKINGDOM MICROBIOME SIGNATURES LINKED WITH COGNITIVE DECLINE IN OLDER ADULTS OF MIAGB CONSORTIUM COHORT Chaudhari, Diptaraj Jain, Shalini Yadav, Hariom Masternak, Michal Holland, Peter Agronin, Marc Innov Aging Late Breaking Abstracts The prevalence of age-related cognitive disorders is increasing. Effective prevention and treatment interventions are unavailable due to a poor understanding of aging biology. Multiple emerging evidence indicates that the gut microbiome is linked with age-related disorders; however, their clinical importance in differentiating and predicting the risk of cognitive decline or dementia is largely elusive. Utilizing samples and data of a large, multi-site clinical study across the state of Florida called Microbiome in aging Gut and Brain (MiaGB) Consortium, our whole genome microbiome sequencing revealed that the viral and archaeal population was significantly reduced in the gut of older adults with dementia (n=8) compared to those with mild cognitive impairment (MCI) (n=25) and normal cognition (n=59). Whereas the fungi were exclusively detected in the controls only. Alpha diversity of the participants with MCI and dementia was lower than the cognitively healthy controls. The abundance of Actinobacteria and Verrucomicrobia phyla was higher, and Firmicutes phylum was lower in the participants with dementia. Bacteriophages Lactobacillus prophage Lj771 and Microbacterium phage Min1 were exclusively detected in the gut of the participants with dementia. The study also identifies key metabolic pathways altered in the controls versus the cognitive impairment state. Our biomarker discovery analyses also revealed that these unique microbiome signatures and pathways might have predictive power for cognitive decline and dementia risk and offer new targets for future therapeutic interventions. Oxford University Press 2022-12-20 /pmc/articles/PMC9766942/ http://dx.doi.org/10.1093/geroni/igac059.2781 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of The Gerontological Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Late Breaking Abstracts
Chaudhari, Diptaraj
Jain, Shalini
Yadav, Hariom
Masternak, Michal
Holland, Peter
Agronin, Marc
UNIQUE TRANSKINGDOM MICROBIOME SIGNATURES LINKED WITH COGNITIVE DECLINE IN OLDER ADULTS OF MIAGB CONSORTIUM COHORT
title UNIQUE TRANSKINGDOM MICROBIOME SIGNATURES LINKED WITH COGNITIVE DECLINE IN OLDER ADULTS OF MIAGB CONSORTIUM COHORT
title_full UNIQUE TRANSKINGDOM MICROBIOME SIGNATURES LINKED WITH COGNITIVE DECLINE IN OLDER ADULTS OF MIAGB CONSORTIUM COHORT
title_fullStr UNIQUE TRANSKINGDOM MICROBIOME SIGNATURES LINKED WITH COGNITIVE DECLINE IN OLDER ADULTS OF MIAGB CONSORTIUM COHORT
title_full_unstemmed UNIQUE TRANSKINGDOM MICROBIOME SIGNATURES LINKED WITH COGNITIVE DECLINE IN OLDER ADULTS OF MIAGB CONSORTIUM COHORT
title_short UNIQUE TRANSKINGDOM MICROBIOME SIGNATURES LINKED WITH COGNITIVE DECLINE IN OLDER ADULTS OF MIAGB CONSORTIUM COHORT
title_sort unique transkingdom microbiome signatures linked with cognitive decline in older adults of miagb consortium cohort
topic Late Breaking Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9766942/
http://dx.doi.org/10.1093/geroni/igac059.2781
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