Key result
Elevated TMAO predicts ~131% greater MACE risk in chronic heart failure after MI.
Why the study?
Trimethylamine N-oxide (TMAO) is implicated in cardiovascular disease pathogenesis, but its prognostic value in chronic heart failure after myocardial infarction is unclear.
Does elevated plasma TMAO predict MACE and all-cause mortality in patients with chronic heart failure after myocardial infarction?
Cohort (n=1,208)
Does elevated plasma TMAO predict MACE and all-cause mortality in patients with chronic heart failure after myocardial infarction?
Hazard Ratio: 2.31 (95% CI 1.42–3.59)
p-value: p=< 0.01
Elevated plasma TMAO is an independent prognostic indicator for MACE and all-cause mortality in patients with chronic heart failure post-myocardial infarction.
May aid post-MI HF risk stratification; hypothesis-generating and requires prospective validation before practice change.
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.
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Zhou et al. (2020) conducted a cohort in Chronic heart failure (CHF) after myocardial infarction (MI) (n=1,208). Elevated plasma trimethylamine N-oxide (TMAO) vs. Lower TMAO levels was evaluated on Major adverse cardiac events (MACE) (HR 2.31, 95% CI 1.42-3.59, p=< 0.01). Elevated plasma TMAO levels significantly predicted major adverse cardiac events in patients with chronic heart failure after myocardial infarction (HR 2.31; 95% CI 1.42-3.59; P<0.01).
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