Stone Peter H, Lloyd-Jones Donald M, Kinlay Scott, Frei Balz, Carlson William, Rubenstein Joel, Andrews Thomas C, Johnstone Michael, Sopko George, Cole Holly, Orav John, Selwyn Andrew P, Creager Mark A
Cardiovascular Division, Brigham & Women's Hospital, Boston, Mass 02115, USA.
Circulation. 2005 Apr 12;111(14):1747-55. doi: 10.1161/01.CIR.0000160866.90148.76. Epub 2005 Apr 4.
Lipid lowering with statins prevents adverse cardiac events. Both lipid-lowering and antioxidant therapies may favorably affect vasomotor function and thereby improve ischemia.
In a randomized, double-blind, placebo-controlled trial, 300 patients with stable coronary disease, a positive exercise treadmill test, 48-hour ambulatory ECG with > or =1 episode of ischemia, and fasting total cholesterol of 180 to 250 mg/dL were assigned to 1-year treatment with intensive atorvastatin to reduce LDL to <80 mg/dL (n=96), intensive atorvastatin to reduce LDL to <80 mg/dL plus antioxidant vitamins C (1000 mg/d) and E (800 mg/d) (n=101), or diet and low-dose lovastatin, if needed, to reduce LDL to <130 mg/dL (n=103; control group). Ischemia end points, including ambulatory ECG monitoring and exercise treadmill testing, and endothelial assessment using brachial artery flow-mediated dilation were obtained at baseline and at 6 and 12 months. Baseline characteristics were similar in all groups. LDL decreased from approximately 153 mg/dL at baseline in the 2 atorvastatin groups to approximately 83 mg/dL at 12 months (each P<0.0001) and from 147 to 120 mg/dL in the control group (P<0.0001). During ambulatory ECG monitoring, mean number of ischemic episodes per 48 hours decreased 31% to 61% in each group (each P<0.001; P=0.15 across groups), without a change in daily heart rate activity. Mean duration of ischemia for 48 hours decreased 26% to 62% in each group (each P<0.001; P=0.06 across groups). Mean exercise duration to 1-mm ST-segment depression significantly increased in each group, but total exercise duration and mean sum of maximum ST depression were unchanged. Angina frequency decreased in each group. There was no incremental effect of supplemental vitamins C and E on any ischemia outcome. Flow-mediated dilation studies indicated no meaningful changes.
Intensive lipid lowering with atorvastatin to an LDL level of 80 mg/dL, with or without antioxidant vitamins, does not provide any further benefits in ambulatory ischemia, exercise time to onset of ischemia, and angina frequency than moderate lipid lowering with diet and low-dose lovastatin to an LDL level of <120 mg/dL.
使用他汀类药物降低血脂可预防不良心脏事件。降脂治疗和抗氧化治疗均可对血管舒缩功能产生有利影响,从而改善局部缺血。
在一项随机、双盲、安慰剂对照试验中,300例稳定型冠心病患者,运动平板试验阳性,动态心电图监测48小时内有≥1次缺血发作,空腹总胆固醇为180至250mg/dL,被分配接受为期1年的强化阿托伐他汀治疗以使低密度脂蛋白降至<80mg/dL(n = 96),强化阿托伐他汀治疗以使低密度脂蛋白降至<80mg/dL并加用抗氧化维生素C(1000mg/d)和E(800mg/d)(n = 101),或饮食及必要时使用低剂量洛伐他汀以使低密度脂蛋白降至<130mg/dL(n = 103;对照组)。在基线、6个月和12个月时获取缺血终点指标,包括动态心电图监测和运动平板试验,以及使用肱动脉血流介导的扩张进行内皮功能评估。所有组的基线特征相似。两个阿托伐他汀组的低密度脂蛋白从基线时的约153mg/dL降至12个月时的约83mg/dL(各P<0.0001),对照组从147mg/dL降至120mg/dL(P<0.000)。在动态心电图监测期间,每组每48小时缺血发作的平均次数减少31%至61%(各P<0.001;组间P = 0.15),每日心率活动无变化。每组48小时缺血的平均持续时间减少26%至62%(各P<0.001;组间P = 0.06)。每组达到1mm ST段压低的平均运动持续时间显著增加,但总运动持续时间和最大ST段压低的平均总和未改变。每组心绞痛频率均降低。补充维生素C和E对任何缺血结局均无额外作用。血流介导的扩张研究显示无有意义的变化。
使用阿托伐他汀强化降脂使低密度脂蛋白水平降至80mg/dL,无论是否加用抗氧化维生素,在动态缺血、缺血发作的运动时间和心绞痛频率方面,与饮食及低剂量洛伐他汀适度降脂使低密度脂蛋白水平降至<120mg/dL相比,并无任何进一步益处。