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Different oral and gut microbial profiles in those with Alzheimer's disease consuming anti-inflammatory diets
The number of people living with Alzheimer's disease (AD) is increasing alongside with aging of the population. Systemic chronic inflammation and microbial imbalance may play an important role in the pathogenesis of AD. Inflammatory diets regulate both the host microbiomes and inflammatory stat...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9521405/ https://www.ncbi.nlm.nih.gov/pubmed/36185672 http://dx.doi.org/10.3389/fnut.2022.974694 |
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author | Chen, Lili Wang, Bixia Liu, Jinxiu Wu, Xiaoqi Xu, Xinhua Cao, Huizhen Ji, Xinli Zhang, Ping Li, Xiuli Hou, Zhaoyi Li, Hong |
author_facet | Chen, Lili Wang, Bixia Liu, Jinxiu Wu, Xiaoqi Xu, Xinhua Cao, Huizhen Ji, Xinli Zhang, Ping Li, Xiuli Hou, Zhaoyi Li, Hong |
author_sort | Chen, Lili |
collection | PubMed |
description | The number of people living with Alzheimer's disease (AD) is increasing alongside with aging of the population. Systemic chronic inflammation and microbial imbalance may play an important role in the pathogenesis of AD. Inflammatory diets regulate both the host microbiomes and inflammatory status. This study aimed to explore the impact of inflammatory diets on oral-gut microbes in patients with AD and the relationship between microbes and markers of systemic inflammation. The dietary inflammatory properties and the oral and gut microorganisms were analyzed using the dietary inflammatory index (DII) and 16S RNA in 60 patients with AD. The α-diversity was not related to the DII (p > 0.05), whereas the β-diversity was different in the oral microbiomes (R(2) = 0.061, p = 0.013). In the most anti-inflammatory diet group, Prevotella and Olsenella were more abundant in oral microbiomes and Alistipes, Ruminococcus, Odoribacter, and unclassified Firmicutes were in the gut microbiomes (p < 0.05). Specific oral and gut genera were associated with interleukin-6 (IL)-6, complement 3 (C3), high-sensitivity C-reactive protein (hs-CRP), IL-1β, IL-4, IL-10, IL-12, and tumor necrosis factor-α (TNF-α) (p < 0.05). In conclusion, anti-inflammatory diets seem to be associated with increased abundance of beneficial microbes, and specific oral and gut microbial composition was associated with inflammatory markers. |
format | Online Article Text |
id | pubmed-9521405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95214052022-09-30 Different oral and gut microbial profiles in those with Alzheimer's disease consuming anti-inflammatory diets Chen, Lili Wang, Bixia Liu, Jinxiu Wu, Xiaoqi Xu, Xinhua Cao, Huizhen Ji, Xinli Zhang, Ping Li, Xiuli Hou, Zhaoyi Li, Hong Front Nutr Nutrition The number of people living with Alzheimer's disease (AD) is increasing alongside with aging of the population. Systemic chronic inflammation and microbial imbalance may play an important role in the pathogenesis of AD. Inflammatory diets regulate both the host microbiomes and inflammatory status. This study aimed to explore the impact of inflammatory diets on oral-gut microbes in patients with AD and the relationship between microbes and markers of systemic inflammation. The dietary inflammatory properties and the oral and gut microorganisms were analyzed using the dietary inflammatory index (DII) and 16S RNA in 60 patients with AD. The α-diversity was not related to the DII (p > 0.05), whereas the β-diversity was different in the oral microbiomes (R(2) = 0.061, p = 0.013). In the most anti-inflammatory diet group, Prevotella and Olsenella were more abundant in oral microbiomes and Alistipes, Ruminococcus, Odoribacter, and unclassified Firmicutes were in the gut microbiomes (p < 0.05). Specific oral and gut genera were associated with interleukin-6 (IL)-6, complement 3 (C3), high-sensitivity C-reactive protein (hs-CRP), IL-1β, IL-4, IL-10, IL-12, and tumor necrosis factor-α (TNF-α) (p < 0.05). In conclusion, anti-inflammatory diets seem to be associated with increased abundance of beneficial microbes, and specific oral and gut microbial composition was associated with inflammatory markers. Frontiers Media S.A. 2022-09-15 /pmc/articles/PMC9521405/ /pubmed/36185672 http://dx.doi.org/10.3389/fnut.2022.974694 Text en Copyright © 2022 Chen, Wang, Liu, Wu, Xu, Cao, Ji, Zhang, Li, Hou and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Nutrition Chen, Lili Wang, Bixia Liu, Jinxiu Wu, Xiaoqi Xu, Xinhua Cao, Huizhen Ji, Xinli Zhang, Ping Li, Xiuli Hou, Zhaoyi Li, Hong Different oral and gut microbial profiles in those with Alzheimer's disease consuming anti-inflammatory diets |
title | Different oral and gut microbial profiles in those with Alzheimer's disease consuming anti-inflammatory diets |
title_full | Different oral and gut microbial profiles in those with Alzheimer's disease consuming anti-inflammatory diets |
title_fullStr | Different oral and gut microbial profiles in those with Alzheimer's disease consuming anti-inflammatory diets |
title_full_unstemmed | Different oral and gut microbial profiles in those with Alzheimer's disease consuming anti-inflammatory diets |
title_short | Different oral and gut microbial profiles in those with Alzheimer's disease consuming anti-inflammatory diets |
title_sort | different oral and gut microbial profiles in those with alzheimer's disease consuming anti-inflammatory diets |
topic | Nutrition |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9521405/ https://www.ncbi.nlm.nih.gov/pubmed/36185672 http://dx.doi.org/10.3389/fnut.2022.974694 |
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