Increased Trimethylamine N-Oxide Portends High Mortality Risk Independent of Glycemic Control in Patients with Type 2 Diabetes Mellitus

被引:209
作者
Tang, W. H. Wilson [1 ,2 ]
Wang, Zeneng [1 ]
Li, Xinmin S. [1 ]
Fan, Yiying [3 ]
Li, Daniel S. [4 ]
Wu, Yuping [3 ]
Hazen, Stanley L. [1 ,2 ]
机构
[1] Cleveland Clin, Ctr Cardiovasc Diagnost & Prevent, Dept Cellular & Mol Med, Lerner Res Inst, Cleveland, OH 44106 USA
[2] Cleveland Clin, Dept Cardiovasc Med, Inst Heart & Vasc, Cleveland, OH 44106 USA
[3] Cleveland State Univ, Dept Math, Cleveland, OH 44115 USA
[4] Case Western Reserve Univ, Lerner Coll Med, Cleveland Clin, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
CONTAINING MONOOXYGENASE 3; GUT MICROBIOTA; PROGNOSTIC VALUE; PLASMA CHOLINE; L-CARNITINE; METABOLISM; BETAINE; GLUCOSE; PHOSPHATIDYLCHOLINE; ATHEROSCLEROSIS;
D O I
10.1373/clinchem.2016.263640
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BACKGROUND: Recent studies show a mechanistic link between intestinal microbial metabolism of dietary phosphatidylcholine and coronary artery disease pathogenesis. Concentrations of a proatherogenic gut microbe-generated metabolite, trimethylamine N-oxide (TMAO), predict increased incident cardiovascular disease risks in multiple cohorts. TMAO concentrations are increased in patients with type 2 diabetes mellitus (T2DM), but their prognostic value and relation to glycemic control are unclear. METHODS: We examined the relationship between fasting TMAO and 2 of its nutrient precursors, choline and betaine, vs 3-year major adverse cardiac events and 5-year mortality in 1216 stable patients with T2DM who underwent elective diagnostic coronary angiography. RESULTS: TMAO [4.4 mu mol/L (interquartile range 2.8 7.7 mu mol/L) vs 3.6 (2.3-5.7 mu mol/L); P < 0.001] and choline concentrations were higher in individuals with T2DM vs healthy controls. Within T2DM patients, higher plasma TMAO was associated with a significant 3.0-fold increased 3-year major adverse cardiac event risk (P < 0.001) and a 3.6-fold increased 5-year mortality risk (P < 0.00.1). Following adjustments for traditional risk factors and high-sensitivity C-reactive protein, glycohemoglobin, and estimated glomerular filtration rate, increased TMAO concentrations remained predictive of both major adverse cardiac events and mortality risks in T2DM patients [e.g., quartiles 4 vs 1, hazard ratio 2.05 (95% CI, 1.31-3.20), P < 0.001; and 2.07 (95% CI, 1.37-3.14), P < 0.001, respectively]. CONCLUSIONS: Fasting plasma concentrations of the proatherogenic gut microbe-generated metabolite TMAO are higher in diabetic patients and portend higher major adverse cardiac events and mortality risks independent of traditional risk factors, renal function, and relationship to glycemic control. (C) 2016 American Association for Clinical Chemistry
引用
收藏
页码:297 / 306
页数:10
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