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The gut microbiome as mediator between diet and its impact on immune function
Dietary habits may affect inflammatory status in humans. Here we explore this interaction as well as the potential mediating role of the gut microbiome (GM), given that the GM is both involved in processing of dietary components and influences the immune system. A cross-sectional analysis of a sampl...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8956630/ https://www.ncbi.nlm.nih.gov/pubmed/35338162 http://dx.doi.org/10.1038/s41598-022-08544-y |
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author | Shi, Huiqing ter Horst, Rob Nielen, Suzanne Bloemendaal, Mirjam Jaeger, Martin Joosten, Irma Koenen, Hans Joosten, Leo A. B. Schweren, Lizanne J. S. Vasquez, Alejandro Arias Netea, Mihai G. Buitelaar, Jan |
author_facet | Shi, Huiqing ter Horst, Rob Nielen, Suzanne Bloemendaal, Mirjam Jaeger, Martin Joosten, Irma Koenen, Hans Joosten, Leo A. B. Schweren, Lizanne J. S. Vasquez, Alejandro Arias Netea, Mihai G. Buitelaar, Jan |
author_sort | Shi, Huiqing |
collection | PubMed |
description | Dietary habits may affect inflammatory status in humans. Here we explore this interaction as well as the potential mediating role of the gut microbiome (GM), given that the GM is both involved in processing of dietary components and influences the immune system. A cross-sectional analysis of a sample of 482 healthy participants (207 males and 275 females) was performed. Dietary intake was assessed by a semiquantitative food questionnaire. Adipokines and soluble inflammatory mediators were assayed with multiple immunoassays and ELISA. Microbial DNA was extracted from frozen stool samples of 471 participants. Polychoric correlation analysis was used to establish dietary patterns, and joint multivariate associations between these dietary patterns and immune biomarkers were studied using regression analyses with adjustment for sex, age, BMI, smoking, education levels and physical exercise and other dietary patterns. Non-parametric entropy mediation was applied to investigate whether diet-immune relationships are mediated by abundance of microbial species. In this cohort, we identified three dietary patterns, characterized as “high-meat” (meat and sweetened drink), “prudent diet” (fish, fruit, legumes and vegetables) and “high alcohol” (higher alcohol consumption). Higher adherence to prudent diet was associated with a higher adiponectin level. The high alcohol pattern was associated with high concentrations of circulating concentrations of pro-inflammatory markers (CRP, IL-6, VEGF). Dialister invisus was found to mediate the relationship between a prudent dietary pattern and adiponectin, AAT, CRP, IL-6, and VEGF. In conclusion, a meat-based diet and a diet with high alcohol consumption were associated with high concentrations of biomarkers of chronic low-grade inflammation, and conversely, a prudent diet was associated with anti-inflammatory biomarkers. Diet-inflammation regulation may differ between sexes. Mediation analyses revealed that the association between prudent diet and immune function was partially mediated by the GM. The study adds to our understanding of the associations between diet, the immune system and the GM in a healthy population. |
format | Online Article Text |
id | pubmed-8956630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89566302022-03-28 The gut microbiome as mediator between diet and its impact on immune function Shi, Huiqing ter Horst, Rob Nielen, Suzanne Bloemendaal, Mirjam Jaeger, Martin Joosten, Irma Koenen, Hans Joosten, Leo A. B. Schweren, Lizanne J. S. Vasquez, Alejandro Arias Netea, Mihai G. Buitelaar, Jan Sci Rep Article Dietary habits may affect inflammatory status in humans. Here we explore this interaction as well as the potential mediating role of the gut microbiome (GM), given that the GM is both involved in processing of dietary components and influences the immune system. A cross-sectional analysis of a sample of 482 healthy participants (207 males and 275 females) was performed. Dietary intake was assessed by a semiquantitative food questionnaire. Adipokines and soluble inflammatory mediators were assayed with multiple immunoassays and ELISA. Microbial DNA was extracted from frozen stool samples of 471 participants. Polychoric correlation analysis was used to establish dietary patterns, and joint multivariate associations between these dietary patterns and immune biomarkers were studied using regression analyses with adjustment for sex, age, BMI, smoking, education levels and physical exercise and other dietary patterns. Non-parametric entropy mediation was applied to investigate whether diet-immune relationships are mediated by abundance of microbial species. In this cohort, we identified three dietary patterns, characterized as “high-meat” (meat and sweetened drink), “prudent diet” (fish, fruit, legumes and vegetables) and “high alcohol” (higher alcohol consumption). Higher adherence to prudent diet was associated with a higher adiponectin level. The high alcohol pattern was associated with high concentrations of circulating concentrations of pro-inflammatory markers (CRP, IL-6, VEGF). Dialister invisus was found to mediate the relationship between a prudent dietary pattern and adiponectin, AAT, CRP, IL-6, and VEGF. In conclusion, a meat-based diet and a diet with high alcohol consumption were associated with high concentrations of biomarkers of chronic low-grade inflammation, and conversely, a prudent diet was associated with anti-inflammatory biomarkers. Diet-inflammation regulation may differ between sexes. Mediation analyses revealed that the association between prudent diet and immune function was partially mediated by the GM. The study adds to our understanding of the associations between diet, the immune system and the GM in a healthy population. Nature Publishing Group UK 2022-03-25 /pmc/articles/PMC8956630/ /pubmed/35338162 http://dx.doi.org/10.1038/s41598-022-08544-y Text en © The Author(s) 2022 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 | Article Shi, Huiqing ter Horst, Rob Nielen, Suzanne Bloemendaal, Mirjam Jaeger, Martin Joosten, Irma Koenen, Hans Joosten, Leo A. B. Schweren, Lizanne J. S. Vasquez, Alejandro Arias Netea, Mihai G. Buitelaar, Jan The gut microbiome as mediator between diet and its impact on immune function |
title | The gut microbiome as mediator between diet and its impact on immune function |
title_full | The gut microbiome as mediator between diet and its impact on immune function |
title_fullStr | The gut microbiome as mediator between diet and its impact on immune function |
title_full_unstemmed | The gut microbiome as mediator between diet and its impact on immune function |
title_short | The gut microbiome as mediator between diet and its impact on immune function |
title_sort | gut microbiome as mediator between diet and its impact on immune function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8956630/ https://www.ncbi.nlm.nih.gov/pubmed/35338162 http://dx.doi.org/10.1038/s41598-022-08544-y |
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