Yu Xing Long, Zhang Hai Juan, Ren Shao Da, Geng Jing, Wu Ting Ting, Chen Wen Qiang, Ji Xiao Ping, Zhong Lin, Ge Zhi Ming
Department of Cardiology, Qilu Hospital, Shandong University, Key Laboratory of Cardiovascular Remodeling and Function Research, Chinese Ministry of Education and Chinese Ministry of Public Health, Jinan, PR China.
Coron Artery Dis. 2011 Mar;22(1):87-91. doi: 10.1097/MCA.0b013e328341baee.
To investigate the effects of loading dose of atorvastatin on periprocedural myocardial injury and inflammatory reaction in patients with non-ST segment elevation (NSTE) acute coronary syndromes (unstable angina or NSTE acute myocardial infarction).
A total of 81 patients with NSTE-acute coronary syndromes were randomly divided into the pretreatment with atorvastatin group [80 mg 12 h before percutaneous coronary intervention (PCI), with a further 40 mg preprocedure dose] (n=41) or the placebo group (n=40). The main end point was a 30-day incidence of major adverse cardiac events (cardiac death, nonfatal acute myocardial infarction, or revascularization with either PCI or coronary artery bypass grafting). Creatine kinase-MB, cardiac troponin I, and high-sensitivity C-reactive protein levels were measured at the baseline and at 8 and 24 h after the procedure.
Major adverse cardiac events occurred in 2.4% of patients in the atorvastatin group and 22.5% of those in the placebo group (P=0.0161). This difference was mostly because of reduction in the incidence of myocardial infarction (2.4 vs. 20.0%; P=0.0307). Markers of the two groups were elevated after PCI; however, the higher values of creatine kinase-MB, cardiac troponin I, and high-sensitivity C-reactive protein in the atorvastatin treatment group were significantly lower than those in the placebo group (P<0.01).
Short-term pretreatment with a high dose of atorvastatin significantly reduces procedural myocardial injury in early PCI.
探讨负荷剂量阿托伐他汀对非ST段抬高(NSTE)急性冠脉综合征(不稳定型心绞痛或NSTE急性心肌梗死)患者围手术期心肌损伤及炎症反应的影响。
将81例NSTE急性冠脉综合征患者随机分为阿托伐他汀预处理组[经皮冠状动脉介入治疗(PCI)前12小时给予80mg,术前再给予40mg](n = 41)或安慰剂组(n = 40)。主要终点是30天主要不良心脏事件(心源性死亡、非致命性急性心肌梗死或PCI或冠状动脉搭桥术血运重建)的发生率。在基线以及术后8小时和24小时测量肌酸激酶同工酶、心肌肌钙蛋白I和高敏C反应蛋白水平。
阿托伐他汀组2.4%的患者发生主要不良心脏事件,安慰剂组为22.5%(P = 0.0161)。这种差异主要是由于心肌梗死发生率的降低(2.4%对20.0%;P = 0.0307)。两组标志物在PCI后均升高;然而,阿托伐他汀治疗组肌酸激酶同工酶、心肌肌钙蛋白I和高敏C反应蛋白的较高值显著低于安慰剂组(P < 0.01)。
高剂量阿托伐他汀短期预处理可显著降低早期PCI术中的心肌损伤。