Abstract

To investigate the association of liver metabolite trimethylamine N-oxide (TMAO) with cardiovascular disease (CV)-related and all-cause mortality in patients with acute coronary syndrome (ACS) who underwent percutaneous coronary intervention. Our prospective observational study enrolled 292 patients with ACS. Plasma concentrations of TMAO were measured during the hospitalization for ACS. Observation period lasted seven yr in median. Adjusted Cox-regression analysis was used for prediction of mortality. ROC curve analysis revealed that increasing concentrations of TMAO levels assessed at the time point of ACS significantly predicted the risk of CV mortality (c-index=0.78, p < 0.001). The cut-off value of >4 μmol/L, labeled as high TMAO level (23% of study population), provided the greatest sum of sensitivity (85%) and specificity (80%) for the prediction of CV mortality and was associated with a positive predictive value of 16% and a negative predictive value of 99%. A multivariate Cox regression model revealed that high TMAO level was a strong and independent predictor of CV death (HR = 11.62, 95% CI: 2.26–59.67; p = 0.003). High TMAO levels as compared with low TMAO levels were associated with the highest risk of CV death in a subpopulation of patients with diabetes mellitus (27.3 vs. 2.6%; p = 0.004). Although increasing TMAO levels were also significantly associated with all-cause mortality, their estimates for diagnostic accuracy were low. High TMAO level is a strong and independent predictor of long-term CV mortality among patients presenting with ACS.

Highlights

  • Acute coronary syndrome (ACS) remains a leading cause of mortality worldwide [1]

  • Elevated concentration of circulating trimethylamine N-oxide (TMAO) has been associated with increased risk of cardiovascular disease (CVD) and major adverse cardiac events (MACE), including myocardial infarction (MI), stroke, major bleeding and all-cause mortality [12]

  • The present study was conducted to evaluate the association of and TMAO with cardiovascular disease (CV)-related and all-cause mortality in patients with ACS. It demonstrates that high concentration of TMAO in the plasma at the time of ACS is associated with 12-fold increased long-term CV mortality

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Summary

Introduction

Acute coronary syndrome (ACS) remains a leading cause of mortality worldwide [1]. Despite development of pharmacological treatment and percutaneous coronary intervention (PCI) [2,3,4,5], patients who experienced ACS are at high risk of future cardiovascular events and death [6,7,8]. Numerous studies revealed that intestinal microbial organisms (microbiota) and its metabolites, as TMA (oxidize trimethylamine) may play a pathogenic role in a wide range of diseases, including the onset and progression of cardiovascular disease (CVD) and ACS [10]. Elevated concentration of circulating TMAO has been associated with increased risk of CVD and major adverse cardiac events (MACE), including myocardial infarction (MI), stroke, major bleeding and all-cause mortality [12]. Data on the effect of TMAO on the circulatory system are conflicting [11, 13,14,15]

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