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Gut-microbe derived TMAO and its association with more progressed forms of AF: Results from the AF-RISK study
INTRODUCTION: The importance of gut microbiome in cardiovascular disease has been increasingly recognized. Trimethylamine N-oxide (TMAO) is a gut microbe-derived metabolite that is associated with cardiovascular disease, including atrial fibrillation (AF). The role of TMAO in clinical AF progression...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8167185/ https://www.ncbi.nlm.nih.gov/pubmed/34095450 http://dx.doi.org/10.1016/j.ijcha.2021.100798 |
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author | Nguyen, B.O. Meems, L.M.G. van Faassen, M. Crijns, H.J.G.M. van Gelder, I.C. Kuipers, F. Rienstra, M. |
author_facet | Nguyen, B.O. Meems, L.M.G. van Faassen, M. Crijns, H.J.G.M. van Gelder, I.C. Kuipers, F. Rienstra, M. |
author_sort | Nguyen, B.O. |
collection | PubMed |
description | INTRODUCTION: The importance of gut microbiome in cardiovascular disease has been increasingly recognized. Trimethylamine N-oxide (TMAO) is a gut microbe-derived metabolite that is associated with cardiovascular disease, including atrial fibrillation (AF). The role of TMAO in clinical AF progression however remains unknown. METHODS AND RESULTS: In this study we measured TMAO and its precursor (betaine, choline, and L- carnitine) levels in 78 patients using plasma samples from patients that participated in the AF-RISK study. 56 patients suffered from paroxysmal AF and 22 had a short history of persistent AF. TMAO levels were significantly higher in patients with persistent AF, as compared to those with paroxysmal AF (median [IQR] 5.65 [4.7–9.6] m/z versus 4.31 [3.2–6.2] m/z, p < 0.05), while precursor levels did not differ. In univariate analysis, we observed that for every unit increase in TMAO, the odds for having persistent AF increased with 0.44 [0.14–0.73], p < 0.01. Conclusion: These results suggest that higher levels of TMAO are associated with more progressed forms of AF. We therefore hypothesize that increased TMAO levels may reflect disease progression in humans. Larger studies are required to validate these preliminary findings. Trial Registration number: Clinicaltrials.gov NCT01510210. |
format | Online Article Text |
id | pubmed-8167185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-81671852021-06-05 Gut-microbe derived TMAO and its association with more progressed forms of AF: Results from the AF-RISK study Nguyen, B.O. Meems, L.M.G. van Faassen, M. Crijns, H.J.G.M. van Gelder, I.C. Kuipers, F. Rienstra, M. Int J Cardiol Heart Vasc Original Paper INTRODUCTION: The importance of gut microbiome in cardiovascular disease has been increasingly recognized. Trimethylamine N-oxide (TMAO) is a gut microbe-derived metabolite that is associated with cardiovascular disease, including atrial fibrillation (AF). The role of TMAO in clinical AF progression however remains unknown. METHODS AND RESULTS: In this study we measured TMAO and its precursor (betaine, choline, and L- carnitine) levels in 78 patients using plasma samples from patients that participated in the AF-RISK study. 56 patients suffered from paroxysmal AF and 22 had a short history of persistent AF. TMAO levels were significantly higher in patients with persistent AF, as compared to those with paroxysmal AF (median [IQR] 5.65 [4.7–9.6] m/z versus 4.31 [3.2–6.2] m/z, p < 0.05), while precursor levels did not differ. In univariate analysis, we observed that for every unit increase in TMAO, the odds for having persistent AF increased with 0.44 [0.14–0.73], p < 0.01. Conclusion: These results suggest that higher levels of TMAO are associated with more progressed forms of AF. We therefore hypothesize that increased TMAO levels may reflect disease progression in humans. Larger studies are required to validate these preliminary findings. Trial Registration number: Clinicaltrials.gov NCT01510210. Elsevier 2021-05-24 /pmc/articles/PMC8167185/ /pubmed/34095450 http://dx.doi.org/10.1016/j.ijcha.2021.100798 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Original Paper Nguyen, B.O. Meems, L.M.G. van Faassen, M. Crijns, H.J.G.M. van Gelder, I.C. Kuipers, F. Rienstra, M. Gut-microbe derived TMAO and its association with more progressed forms of AF: Results from the AF-RISK study |
title | Gut-microbe derived TMAO and its association with more progressed forms of AF: Results from the AF-RISK study |
title_full | Gut-microbe derived TMAO and its association with more progressed forms of AF: Results from the AF-RISK study |
title_fullStr | Gut-microbe derived TMAO and its association with more progressed forms of AF: Results from the AF-RISK study |
title_full_unstemmed | Gut-microbe derived TMAO and its association with more progressed forms of AF: Results from the AF-RISK study |
title_short | Gut-microbe derived TMAO and its association with more progressed forms of AF: Results from the AF-RISK study |
title_sort | gut-microbe derived tmao and its association with more progressed forms of af: results from the af-risk study |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8167185/ https://www.ncbi.nlm.nih.gov/pubmed/34095450 http://dx.doi.org/10.1016/j.ijcha.2021.100798 |
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