Why the study?
Trimethylamine N-oxide has been considered an independent risk factor of HF, but its plasma levels and relationship with HFpEF risk required further determination.
Are plasma levels of Trimethylamine N-oxide (TMAO) associated with the risk of heart failure with preserved ejection fraction (HFpEF)?
Case-Control (n=118)
Are plasma levels of Trimethylamine N-oxide (TMAO) associated with the risk of heart failure with preserved ejection fraction (HFpEF)?
Absolute Event Rate: 6.84% vs 1.63%
p-value: p=<.01
Elevated plasma levels of TMAO are significantly associated with the risk of heart failure with preserved ejection fraction and correlate with markers of renal function and myocardial stress.
BACKGROUND: Trimethylamine N-oxide (TMAO) has been considered to be an independent risk factor of heart failure (HF). OBJECTIVES: To further determine the plasma levels of TMAO in patients who have HF with preserved ejection fraction (HFpEF), and to analyze the relationship between TMAO and HFpEF risk. METHODS: A total of 57 control participants and 61 patients with HFpEF were recruited. We measured and analyzed plasma levels of TMAO and performed biochemical examination of all patients. RESULTS: The mean (SD) plasma levels of TMAO in patients with HFpEF (6.84 [1.12] μmol/L) were significantly higher than in controls (1.63 [0.08] μmol/L; P <.01). The area under the curve (AUC) of TMAO and N-terminal pro b-type natriuretic peptide (NT-proBNP) was 0.817 and 0.924, respectively, which were determined by receiver operating characteristic (ROC) analysis. TMAO was an independent risk factor in patients with HFpEF, as revealed by univariate and multivariate logistic regression analysis. The level of TMAO was correlated with blood urea nitrogen (BUN), creatinine, and NT-proBNP. CONCLUSIONS: TMAO level was highly associated with HFpEF risk.
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Dong et al. (2020) conducted a case-control in Heart Failure with Preserved Ejection Fraction (HFpEF) (n=118). Heart failure with preserved ejection fraction (HFpEF) vs. Controls was evaluated on Plasma levels of TMAO (μmol/L) (p=<.01).
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