医学
射血分数
心肌梗塞
安慰剂
心脏病学
内科学
随机对照试验
精氨酸
梗塞
心力衰竭
病理
生物化学
化学
替代医学
氨基酸
作者
Steven P. Schulman,Lewis C. Becker,David A. Kass,Hunter C. Champion,Michael L. Terrin,Sandra Forman,K Ernst,Mark D. Kelemen,Susan N. Townsend,Anne Capriotti,Joshua M. Hare,Gary Gerstenblith
出处
期刊:JAMA
[American Medical Association]
日期:2006-01-04
卷期号:295 (1): 58-58
被引量:323
标识
DOI:10.1001/jama.295.1.58
摘要
The amino acid L-arginine is a substrate for nitric oxide synthase and is increasingly used as a health supplement. Prior studies suggest that L-arginine has the potential to reduce vascular stiffness.To determine whether the addition of L-arginine to standard postinfarction therapy reduces vascular stiffness and improves ejection fraction over 6-month follow-up in patients following acute ST-segment elevation myocardial infarction.Single-center, randomized, double-blind, placebo-controlled trial with enrollment from February 2002 to June 2004.A total of 153 patients following a first ST-segment elevation myocardial infarction were enrolled; 77 patients were 60 years or older.Patients were randomly assigned to receive L-arginine (goal dose of 3 g 3 times a day) or matching placebo for 6 months.Change in gated blood pool-derived ejection fraction over 6 months in patients 60 years or older randomized to receive L-arginine compared with those assigned to receive placebo. Secondary outcomes included change in ejection fraction in all patients enrolled, change in noninvasive measures of vascular stiffness, and clinical events.Baseline characteristics, vascular stiffness measurements, and left ventricular function were similar between participants randomized to receive placebo or L-arginine. The mean (SD) age was 60 (13.6) years; of the participants, 104 (68%) were men. There was no significant change from baseline to 6 months in the vascular stiffness measurements or left ventricular ejection fraction in either of the 2 groups, including those 60 years or older and the entire study group. However, 6 participants (8.6%) in the L-arginine group died during the 6-month study period vs none in the placebo group (P = .01). Because of the safety concerns, the data and safety monitoring committee closed enrollment.L-arginine, when added to standard postinfarction therapies, does not improve vascular stiffness measurements or ejection fraction and may be associated with higher postinfarction mortality. L-arginine should not be recommended following acute myocardial infarction. Clinical Trial Registration ClinicalTrials.gov, NCT00051376.
科研通智能强力驱动
Strongly Powered by AbleSci AI