Prognostic Value of Elevated Levels of Intestinal Microbe-Generated Metabolite Trimethylamine-N-Oxide in Patients With Heart Failure: Refining the Gut Hypothesis

Altered intestinal function is prevalent in patients with heart failure (HF), but its role in adverse outcomes is unclear. This study investigated the potential pathophysiological contributions of intestinal microbiota in HF. We examined the relationship between fasting plasma trimethylamine-N-oxide...

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Published inJournal of the American College of Cardiology Vol. 64; no. 18; pp. 1908 - 1914
Main Authors TANG, W. H. Wilson, ZENENG WANG, YIYING FAN, LEVISON, Bruce, HAZEN, Jennie E, DONAHUE, Lillian M, YUPING WU, HAZEN, Stanley L
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier 04.11.2014
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Summary:Altered intestinal function is prevalent in patients with heart failure (HF), but its role in adverse outcomes is unclear. This study investigated the potential pathophysiological contributions of intestinal microbiota in HF. We examined the relationship between fasting plasma trimethylamine-N-oxide (TMAO) and all-cause mortality over a 5-year follow-up in 720 patients with stable HF. The median TMAO level was 5.0 μM, which was higher than in subjects without HF (3.5 μM; p < 0.001). There was modest but significant correlation between TMAO concentrations and B-type natriuretic peptide (BNP) levels (r = 0.23; p < 0.001). Higher plasma TMAO levels were associated with a 3.4-fold increased mortality risk. Following adjustments for traditional risk factors and BNP levels, elevated TMAO levels remained predictive of 5-year mortality risk (hazard ratio [HR]: 2.2; 95% CI: 1.42 to 3.43; p < 0.001), as well as following the addition of estimated glomerular filtration rate to the model (HR: 1.75; 95% CI: 1.07 to 2.86; p < 0.001). High TMAO levels were observed in patients with HF, and elevated TMAO levels portended higher long-term mortality risk independent of traditional risk factors and cardiorenal indexes.
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ISSN:0735-1097
1558-3597
1558-3597
DOI:10.1016/j.jacc.2014.02.617