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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...

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Autores principales: Nguyen, B.O., Meems, L.M.G., van Faassen, M., Crijns, H.J.G.M., van Gelder, I.C., Kuipers, F., Rienstra, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
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.
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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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