4.6 Article

Asymmetric dimethylarginine predicts clinical outcomes in ischemic chronic heart failure

期刊

ATHEROSCLEROSIS
卷 225, 期 2, 页码 504-510

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.atherosclerosis.2012.09.040

关键词

Asymmetric dimethylarginine; Coronary artery disease; Heart failure; Nitric oxide

资金

  1. National Science Council, Taipei, Taiwan, ROC [NSC96-2314-B-075-071-MY3]

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Background: Elevated plasma level of asymmetric dimethylarginine (ADMA) has been reported to be associated with endothelial dysfunction and atherosclerotic risk factors, and may predict adverse cardiovascular events in patients with coronary artery disease. In this study, we aimed to assess the association between plasma ADMA and long-term outcome in patients with angiography-documented ischemic chronic heart failure (HF). Methods and results: We evaluated 285 patients with ischemic chronic HF and measured their plasma ADMA levels by high performance liquid chromatography. The mean age was 70 +/- 12 years and the mean left ventricular ejection fraction was 36 + 8%. Plasma ADMA levels were positively correlated with NYHA functional class (p < 0.001) and log N-terminal pro-B type natriuretic peptide (NT-proBNP) level (p < 0.001). During the median follow-up period of 2.2 years, we observed 58 major adverse cardiovascular events (MACE) (20.4%) and 95 MACE plus cardiac decompensation (33.3%). Multivariate Cox regression analysis adjusted for age, ejection fraction, renal function and log NT-proBNP level revealed that ADMA might be a significant independent risk factor and the relative risk of MACE and MACE plus cardiac decompensation would increase by 23% and 25% respectively when plasma ADMA level increased by 1 SD of value (p = 0.05 and 0.007). Conclusions: In patients with ischemic chronic HF, elevated plasma ADMA levels might be associated with higher NYHA functional classes and elevated NT-proBNP level, and appear to be an independent predictor of long-term adverse clinical outcomes. (C) 2012 Elsevier Ireland Ltd. All rights reserved.

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