Asymmetrical dimethylarginine independently predicts total and cardiovascular mortality in individuals with angiographic coronary artery disease (The Ludwigshafen Risk and Cardiovascular Health Study)

被引:198
作者
Meinitzer, Andreas
Seelhorst, Ursula
Wellnitz, Britta
Halwachs-Baumann, Gabriele
Boehm, Bernhard O.
Winkelmann, Bernhard R.
Maerz, Winfried
机构
[1] Med Univ Graz, Clin Inst Med & Chem Lab Diagnost, Graz, Austria
[2] LURIC Database Nonprofit LLC, Freiberg, Germany
[3] Univ Hosp, Dept Med, Div Endocrinol, Ulm, Germany
[4] Frankfurt Sachsenhausen, Cardiol Grp, Frankfurt, Germany
[5] Synlab Ctr Lab Diagnost Heidelberg, Heidelberg, Germany
关键词
D O I
10.1373/clinchem.2006.076711
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: Asymmetrical dimethylarginine (ADMA) is increased in conditions associated with increased risk of atherosclerosis. We investigated the use of ADMA to predict total and cardiovascular mortality in patients scheduled for coronary angiography. Methods: In 2543 persons with and 695 without coronary artery disease (CAD) identified by angiography we measured ADMA and recorded total and cardiovascular mortality during a median follow-up of 5.45 years. Results: ADMA was correlated positively to age, female sex, diabetes mellitus, former and current smoking, and C-reactive protein and inversely to HDL cholesterol and triglycerides. ADMA was not associated with body mass index, hypertension, LDL cholesterol, or the presence or absence of angiographic CAD. Glomerular filtration rate and homocysteine were the strongest predictors of ADMA. At the 2nd, 3rd and 4th quartile of ADMA, hazard ratios for all-cause mortality adjusted for age, sex, and cardiovascular risk factors were 1.12 [95% confidence interval (CI) 1.83-1.52], 1.35 (95% Cl 1.01- 1.81), and 1.87 (95% Cl 1.43-2.44), respectively, compared with the 1st quartile. Hazard ratios for cardiovascular death were 1.13 (95% Cl 0.78-1.63), 1.42 (95% Cl 1.00-2.02), and 1.81 (95% CI 1.31-2.51). ADMA in the highest quartile remained predictive of mortality after accounting for medication at baseline. The predictive value of ADMA was similar to that in the entire cohort in persons with CAD, stable or unstable, but was not statistically significant in persons without angiographic CAD. Conclusions: ADMA concentration predicts all-cause and cardiovascular mortality in individuals with CAD independently of established and emerging cardiovascular risk factors. (c) 2007 American Association for Clinical Chemistry
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页码:273 / 283
页数:11
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