4.6 Article

Plasma levels of trimethylamine-N-oxide are confounded by impaired kidney function and poor metabolic control

Journal

ATHEROSCLEROSIS
Volume 243, Issue 2, Pages 638-644

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.atherosclerosis.2015.10.091

Keywords

TMAO; Choline; Betaine; Kidney function; Metabolic control; Cardiovascular risk

Funding

  1. Framework Program 7 grant from the European Commission (RESOLVE) [305707]

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Background: After ingestion of phosphatidylcholine, L-carnitine or betaine, trimethylamine-N-oxide (TMAO) is formed by gut microbiota and liver enzymes. Elevated TMAO plasma levels were associated with increased cardiovascular risk and other diseases. Also betaine and choline itself were recently associated with increased cardiovascular risk. Methods: A newly developed LC-HRMS method was applied to measure the plasma concentrations of TMAO, betaine and choline in a cohort of 339 patients undergoing coronary angiography for the evaluation of suspected coronary artery disease. Results: Betaine concentrations in males were significantly higher than in females (42.0 vs. 35.9 mu mol/L; p < 0.001). Plasma concentrations of TMAO but not of betaine or choline were higher in patients with diabetes compared to euglycemic patients (2.39 vs. 0.980 mu mol/L; p = 0.001) as well as in patients with metabolic syndrome as compared to patients without metabolic syndrome (2.37 vs. 1.43 mu mol/L; p = 0.002). Plasma concentrations of TMAO or choline increased significantly with decreasing renal function (Spearman's rho: -0.281; p < 0.001). However, plasma levels of TMAO or betaine were associated with neither a history of myocardial infarction nor the angiographically assessed presence of coronary heart disease, nor incident cardiovascular events during 8 years of follow-up. Plasma levels of choline were significantly lower in patients with a history of acute myocardial infarction as compared to those without such history (10.0 vs. 10.8 mu mol/L; p = 0.045). Conclusions: Plasma levels of TMAO are confounded by impaired kidney function and poor metabolic control but are not associated with the history, presence or incidence of symptoms or events of coronary heart disease. (C) 2015 Elsevier Ireland Ltd. All rights reserved.

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