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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.
Afiliación
  • Nguyen BO; Department of Cardiology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
  • Meems LMG; Department of Cardiology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
  • van Faassen M; Department of Laboratory Medicine, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
  • Crijns HJGM; Maastricht University Medical Center+ and Cardiovascular Research Institute Maastricht, Maastricht, the Netherlands.
  • van Gelder IC; Department of Cardiology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
  • Kuipers F; Department of Laboratory Medicine, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
  • Rienstra M; Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Int J Cardiol Heart Vasc ; 34: 100798, 2021 Jun.
Article en En | MEDLINE | ID: mdl-34095450
ABSTRACT

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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Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Etiology_studies / Risk_factors_studies Idioma: En Revista: Int J Cardiol Heart Vasc Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Etiology_studies / Risk_factors_studies Idioma: En Revista: Int J Cardiol Heart Vasc Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos