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Association of the human gut microbiota with vascular stiffness
Gut microbiota metabolites have been mechanistically linked to inflammatory pathway activation and atherosclerosis, which are major causes of vascular stiffness (VS). Aiming to investigate if the gut microbiome might be involved in VS development, we performed a cross-sectional study (n = 3,087), ne...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10432492/ https://www.ncbi.nlm.nih.gov/pubmed/37587126 http://dx.doi.org/10.1038/s41598-023-40178-6 |
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author | Cuadrat, Rafael R. C. Goris, Tobias Birukov, Anna Eichelmann, Fabian Andrade, Bruno G. N. Bang, Corinna Franke, Andre Wittenbecher, Clemens Schulze, Matthias B. |
author_facet | Cuadrat, Rafael R. C. Goris, Tobias Birukov, Anna Eichelmann, Fabian Andrade, Bruno G. N. Bang, Corinna Franke, Andre Wittenbecher, Clemens Schulze, Matthias B. |
author_sort | Cuadrat, Rafael R. C. |
collection | PubMed |
description | Gut microbiota metabolites have been mechanistically linked to inflammatory pathway activation and atherosclerosis, which are major causes of vascular stiffness (VS). Aiming to investigate if the gut microbiome might be involved in VS development, we performed a cross-sectional study (n = 3,087), nested within the population-based European Prospective Investigations into Cancer and Nutrition (EPIC) Potsdam. We investigated the correlation of the gut microbiota (alpha diversity and taxa abundance) with 3 vascular stiffness measures: carotid-femoral (PWV), aortic augmentation index (AIX) and ankle-brachial index (ABI). Shannon index was not significantly associated with VS but the number of observed Amplicon Sequence Variants (ASV) was positively associated with PWV and AIX. We found a total of 19 ASVs significantly associated with at least one VS measure in multivariable-adjusted models. One ASV (classified as Sutterella wadsworthensis) was associated with 2 VS measures, AIX (− 0.11 ± 0.04) and PWV (-0.14 ± 0.03). Other examples of ASVs associated with VS were Collinsella aerofaciens, previously reported to be affected by diet and Bacteroides uniformis, commercially available as probiotics. In conclusion, our study suggests a potential role of individual components of the gut microbiota in the aetiology of VS. |
format | Online Article Text |
id | pubmed-10432492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104324922023-08-18 Association of the human gut microbiota with vascular stiffness Cuadrat, Rafael R. C. Goris, Tobias Birukov, Anna Eichelmann, Fabian Andrade, Bruno G. N. Bang, Corinna Franke, Andre Wittenbecher, Clemens Schulze, Matthias B. Sci Rep Article Gut microbiota metabolites have been mechanistically linked to inflammatory pathway activation and atherosclerosis, which are major causes of vascular stiffness (VS). Aiming to investigate if the gut microbiome might be involved in VS development, we performed a cross-sectional study (n = 3,087), nested within the population-based European Prospective Investigations into Cancer and Nutrition (EPIC) Potsdam. We investigated the correlation of the gut microbiota (alpha diversity and taxa abundance) with 3 vascular stiffness measures: carotid-femoral (PWV), aortic augmentation index (AIX) and ankle-brachial index (ABI). Shannon index was not significantly associated with VS but the number of observed Amplicon Sequence Variants (ASV) was positively associated with PWV and AIX. We found a total of 19 ASVs significantly associated with at least one VS measure in multivariable-adjusted models. One ASV (classified as Sutterella wadsworthensis) was associated with 2 VS measures, AIX (− 0.11 ± 0.04) and PWV (-0.14 ± 0.03). Other examples of ASVs associated with VS were Collinsella aerofaciens, previously reported to be affected by diet and Bacteroides uniformis, commercially available as probiotics. In conclusion, our study suggests a potential role of individual components of the gut microbiota in the aetiology of VS. Nature Publishing Group UK 2023-08-16 /pmc/articles/PMC10432492/ /pubmed/37587126 http://dx.doi.org/10.1038/s41598-023-40178-6 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 | Article Cuadrat, Rafael R. C. Goris, Tobias Birukov, Anna Eichelmann, Fabian Andrade, Bruno G. N. Bang, Corinna Franke, Andre Wittenbecher, Clemens Schulze, Matthias B. Association of the human gut microbiota with vascular stiffness |
title | Association of the human gut microbiota with vascular stiffness |
title_full | Association of the human gut microbiota with vascular stiffness |
title_fullStr | Association of the human gut microbiota with vascular stiffness |
title_full_unstemmed | Association of the human gut microbiota with vascular stiffness |
title_short | Association of the human gut microbiota with vascular stiffness |
title_sort | association of the human gut microbiota with vascular stiffness |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10432492/ https://www.ncbi.nlm.nih.gov/pubmed/37587126 http://dx.doi.org/10.1038/s41598-023-40178-6 |
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