Oka Roberta K, Szuba Andrzej, Giacomini John C, Cooke John P
University of California San Francisco, Department of Community Health Systems, School of Nursing 2 Koret Way, Box 0608, San Francisco, CA 94143-0608, USA.
Vasc Med. 2005 Nov;10(4):265-74. doi: 10.1191/1358863x05vm637oa.
Peripheral arterial disease (PAD) impairs walking capacity and is often associated with a profound endothelial vasodilator dysfunction, characterized by reduced bioactivity and/or synthesis of endothelium-derived nitric oxide (NO). Previous studies have suggested that dietary supplementation of L-arginine, the precursor of NO, improves endothelium-dependent vasodilation, limb blood flow and walking distance. However, these studies have been small, and have used large intravenous doses of L-arginine. The optimal dose of L-arginine has not been determined. Accordingly, this pilot study was conducted to establish the lowest effective oral dose of L-arginine to improve walking distance in preparation for the definitive study. Patients with PAD and intermittent claudication (n = 80) participated in this study. Eligibility criteria included: (1) ankle-brachial index (ABI) at rest < or = 0.90; (2) post-exercise reduction in ABI > or = 25%; and (3) difference in absolute claudication distance of < or = 25% between two consecutive treadmill tests. Treadmill testing was performed using the Skinner-Gardner protocol and community-based walking was assessed using the walking impairment questionnaire. Patients were randomly assigned to oral doses of 0, 3, 6 or 9 g of L-arginine daily in three divided doses for 12 weeks. Treadmill testing was performed prior to administration of the study drug and again after 12 weeks of treatment. The study drug was well tolerated, with no significant adverse effects of L-arginine therapy. The safety laboratory studies were unremarkable, except for a statistically significant reduction in hematocrit in the L-arginine-treated groups. There was no significant difference observed in absolute claudication distance between the groups. However, a trend was observed for a greater increase in walking distance in the group treated with 3 g L-arginine daily, and there was a trend for an improvement in walking speed in patients treated with L-arginine. This pilot study provided data for safety, for power calculation and for dosing for the larger definitive trial that is now underway.
外周动脉疾病(PAD)会损害行走能力,且常与严重的内皮血管舒张功能障碍相关,其特征为内皮源性一氧化氮(NO)的生物活性降低和/或合成减少。先前的研究表明,补充膳食中的L-精氨酸(NO的前体)可改善内皮依赖性血管舒张、肢体血流量和行走距离。然而,这些研究规模较小,且使用的是大剂量静脉注射L-精氨酸。L-精氨酸的最佳剂量尚未确定。因此,开展了这项初步研究,以确定改善行走距离的L-精氨酸最低有效口服剂量,为确定性研究做准备。患有PAD和间歇性跛行的患者(n = 80)参与了本研究。入选标准包括:(1)静息踝臂指数(ABI)≤0.90;(2)运动后ABI降低≥25%;(3)两次连续跑步机测试之间绝对跛行距离的差异≤25%。使用Skinner-Gardner方案进行跑步机测试,并使用步行障碍问卷评估基于社区的步行情况。患者被随机分配,每日口服0、3、6或9克L-精氨酸,分三次服用,持续12周。在服用研究药物前和治疗12周后再次进行跑步机测试。研究药物耐受性良好,L-精氨酸治疗未产生明显不良反应。除L-精氨酸治疗组的血细胞比容有统计学显著降低外,安全性实验室研究无异常。各组之间在绝对跛行距离上未观察到显著差异。然而,观察到每日服用3克L-精氨酸的组行走距离增加幅度更大,且服用L-精氨酸的患者行走速度有改善趋势。这项初步研究为正在进行的更大规模确定性试验的安全性、功效计算和给药提供了数据。