摘要
目的:观察血管紧张素转换酶抑制剂(ACEI)和/或醛固酮受体拮抗剂对冠心病患者介入治疗(PCI)后血浆骨桥蛋白(OPN)的影响。方法因冠心病接受 PCI治疗的100例患者随机分为常规治疗组、福新普利组(10 mg/d),依普利酮组(10 mg/d),联合用药组(各5 mg/d)。治疗1次/d,持续14d。因冠心病行冠脉造影但无需PCI术患者25例作为对照组。分别于术前、术后3d和术后14d测定血浆OPN浓度。结果各组间介入治疗前血浆OPN表达无显著差异,术后呈时间依赖性升高。给予ACEI及醛固酮受体拮抗剂干预后,术后14d OPN表达水平显著降低,以联合用药组下降最为明显。结论 PCI术后血浆OPN水平升高,而ACEI与醛固酮受体拮抗剂均能降低OPN表达,且联合用药最为明显。 ACEI与醛固酮受体拮抗剂联合应用可降低血浆 OPN表达,抑制血管内皮损伤,防治PCI术后再狭窄。
Objective:This study was to investigate the ef ect of fosinopril and eplerenone on the plasma level of osteopontin(OPN)in coronary artery disease(CAD)patients receiving percutaneous coronary intervention(PCI).Method:A total of 100 patients with coronary artery disease receiving PCI were randomly divided into 4 groups:PCI group,fosinopril(F;10 mg/d)group,eplerenone(E;10 mg/d)group and F+E group(5 mg/d for each)(n=25 per group).Another 25 CAD patients receiving coronary angiography alone were also recruited as controls.The plasma OPN levels were measured preoperatively and 3 and 14 days postoperatively.Results:There was no significant dif erence in preoperative plasma OPN level among al groups.After PCI,the plasma OPN increased with a time-dependent manner.After treatment with fosinopril and/or eplerenone,the postoperative plasma OPN level decreased markedly at 14 days,and the highest reduction was found in the F+E group.Conclusion:PCI may lead to an increase in plasma OPN,and ACEI and/or aldosterone receptor antagonist can decrease the PCI-induced OPN increase.ACEI and/or aldosterone receptor antagonist can exert synergistic ef ect to prevent postoperative restenosis in CAD patients receiving PCI.
作者
刘丽敏
谭力力
高宁
LIU Li-min;TAN Li-li;GAO Ning(Shenyang Medical College Shenzhou Hospital,Department of Cardiology,Shenyang Liaoning110000,China;Shenyang Medical College Shenzhou Hospital North Branch Department of Cardiology,Shenyang Liaoning110000,China;Shenyang Normal University Outpatient Department,Shenyang Liaoning110000,China)
基金
沈阳市科技局科技支撑项目(2011F11-264-1-48).
关键词
冠心病
骨桥蛋白
血管紧张素转换酶抑制剂
醛固酮受体拮抗剂
冠状动脉介入治疗
Coronary artery disease
Osteopontin
Angiotensin converting enzyme inhibitor
Percutaneous coronary intervention
Aldosterone receptor antagonist