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Submitted on May 30, 2006
Accepted on August 8, 2006
From the Department of Clinical Pharmacology (F.M., M.M., M.W.), Medical University Vienna; the Department of Internal Medicine I (K.K.), Rudolfstiftung Hospital, Vienna; the Clinical Institute for Medical and Chemical Laboratory Diagnostics (M.E.), Medical University Vienna; and the Department of Internal Medicine II (W.M., J.A., S.S., E.M., M.S.), Division of Angiology, Medical University Vienna, Austria.
* To whom correspondence should be addressed. E-mail: friedrich.mittermayer{at}meduniwien.ac.at.
Objective--Circulating concentrations of asymmetrical dimethylarginine (ADMA), an endogenous inhibitor of nitric oxide synthesis, are elevated in conditions associated with increased cardiovascular risk. We investigated whether elevated ADMA concentrations predict major adverse cardiovascular events (MACE) in patients with advanced peripheral artery disease (PAD).
Methods and Results--We prospectively enrolled 496 of 533 consecutive patients with PAD (median age 70 years, 279 males). ADMA and L-arginine were assessed at baseline by high performance liquid chromatography. The occurrence of MACE (myocardial infarction, percutaneous coronary intervention, coronary artery bypass graft, stroke, carotid revascularization, death) was evaluated during a follow-up of median 19 months (interquartile range 11 to 25). One hundred eighty-two MACE were observed in 141 patients (28%). MACE occurred in 39% of the patients in the highest quartile and 26% of those in the lowest quartile of ADMA (P=0.016, log-rank test for all quartiles). Adjusted hazard ratios for occurrence of MACE for increasing quartiles of ADMA compared with the lowest quartile were 0.87 (95% confidence interval [CI], 0.51 to 1.48), 1.12 (95% CI, 0.62 to 1.90), and 1.70 (95% CI, 1.02 to 2.88), respectively. We observed no association between cardiovascular outcome and L-arginine.
Conclusions--High ADMA plasma concentrations independently predict MACE in patients with advanced PAD. This indicates that ADMA may be a new cardiovascular risk marker in these patients.
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