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Trimethylamine N‐oxide and cardiovascular outcomes in patients with chronic heart failure after myocardial infarction
AIM: Accumulating evidence has demonstrated that intestinal microbiota‐dependent trimethylamine N‐oxide (TMAO) is involved in the pathogenesis of various cardiovascular diseases. The present study was designed to investigate the prognostic value of TMAO in patients with chronic heart failure (CHF) a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7083407/ https://www.ncbi.nlm.nih.gov/pubmed/31960610 http://dx.doi.org/10.1002/ehf2.12552 |
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author | Zhou, Xiang Jin, Mengchao Liu, Lei Yu, Zongliang Lu, Xiang Zhang, Hao |
author_facet | Zhou, Xiang Jin, Mengchao Liu, Lei Yu, Zongliang Lu, Xiang Zhang, Hao |
author_sort | Zhou, Xiang |
collection | PubMed |
description | AIM: Accumulating evidence has demonstrated that intestinal microbiota‐dependent trimethylamine N‐oxide (TMAO) is involved in the pathogenesis of various cardiovascular diseases. The present study was designed to investigate the prognostic value of TMAO in patients with chronic heart failure (CHF) after myocardial infarction (MI). METHODS AND RESULTS: We included 1208 CHF patients after MI in a prospective cohort study and determined the association between plasma TMAO and cardiovascular outcomes using Cox regression analysis. Patients with elevated TMAO levels were more likely to be older and have histories of atrial fibrillation and diabetes. Cox regression analysis indicated that TMAO was a significant predictor of major adverse cardiac events (MACE) (hazard ratio = 2.31, 95% confidence interval 1.42–3.59, P < 0.01) following adjustment for conventional risk factors. Integrated discrimination and net reclassification improvements for MACE were markedly improved by addition of TMAO to the model of traditional risk factors. The Kaplan–Meier survival analysis showed that MACE risk increased with the elevation in TMAO levels and this positive correlation became more significant when TMAO levels were higher than the median. TMAO was also found to be an independent predictor of all‐cause mortality (hazard ratio = 2.15, 95% confidence interval 1.37–3.24, P < 0.01) after adjusting for traditional risk factors. CONCLUSIONS: Our study suggests that TMAO is a valuable prognostic indicator of MACE in patients with CHF after MI. |
format | Online Article Text |
id | pubmed-7083407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70834072020-03-24 Trimethylamine N‐oxide and cardiovascular outcomes in patients with chronic heart failure after myocardial infarction Zhou, Xiang Jin, Mengchao Liu, Lei Yu, Zongliang Lu, Xiang Zhang, Hao ESC Heart Fail Original Research Articles AIM: Accumulating evidence has demonstrated that intestinal microbiota‐dependent trimethylamine N‐oxide (TMAO) is involved in the pathogenesis of various cardiovascular diseases. The present study was designed to investigate the prognostic value of TMAO in patients with chronic heart failure (CHF) after myocardial infarction (MI). METHODS AND RESULTS: We included 1208 CHF patients after MI in a prospective cohort study and determined the association between plasma TMAO and cardiovascular outcomes using Cox regression analysis. Patients with elevated TMAO levels were more likely to be older and have histories of atrial fibrillation and diabetes. Cox regression analysis indicated that TMAO was a significant predictor of major adverse cardiac events (MACE) (hazard ratio = 2.31, 95% confidence interval 1.42–3.59, P < 0.01) following adjustment for conventional risk factors. Integrated discrimination and net reclassification improvements for MACE were markedly improved by addition of TMAO to the model of traditional risk factors. The Kaplan–Meier survival analysis showed that MACE risk increased with the elevation in TMAO levels and this positive correlation became more significant when TMAO levels were higher than the median. TMAO was also found to be an independent predictor of all‐cause mortality (hazard ratio = 2.15, 95% confidence interval 1.37–3.24, P < 0.01) after adjusting for traditional risk factors. CONCLUSIONS: Our study suggests that TMAO is a valuable prognostic indicator of MACE in patients with CHF after MI. John Wiley and Sons Inc. 2020-01-20 /pmc/articles/PMC7083407/ /pubmed/31960610 http://dx.doi.org/10.1002/ehf2.12552 Text en © 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Research Articles Zhou, Xiang Jin, Mengchao Liu, Lei Yu, Zongliang Lu, Xiang Zhang, Hao Trimethylamine N‐oxide and cardiovascular outcomes in patients with chronic heart failure after myocardial infarction |
title | Trimethylamine N‐oxide and cardiovascular outcomes in patients with chronic heart failure after myocardial infarction |
title_full | Trimethylamine N‐oxide and cardiovascular outcomes in patients with chronic heart failure after myocardial infarction |
title_fullStr | Trimethylamine N‐oxide and cardiovascular outcomes in patients with chronic heart failure after myocardial infarction |
title_full_unstemmed | Trimethylamine N‐oxide and cardiovascular outcomes in patients with chronic heart failure after myocardial infarction |
title_short | Trimethylamine N‐oxide and cardiovascular outcomes in patients with chronic heart failure after myocardial infarction |
title_sort | trimethylamine n‐oxide and cardiovascular outcomes in patients with chronic heart failure after myocardial infarction |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7083407/ https://www.ncbi.nlm.nih.gov/pubmed/31960610 http://dx.doi.org/10.1002/ehf2.12552 |
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