他汀序贯疗法在择期经皮冠状动脉介入治疗患者中降脂和抗炎作用的疗效观察Efficacy of lipid-lowering and anti-inflammatory effects of statins sequential therapy in coronary heart disease patients undergoing elective PCI
王芍,张海涛,刘朝中
摘要(Abstract):
目的评估阿托伐他汀钙序贯治疗对择期经皮冠状动脉介入治疗(PCI)患者的血脂及特异性炎性因子的影响,同时评估其安全性。方法 88例择期PCI患者随机分为序贯组(43例)及常规组(45例)。在用药前及用药后3 d、1个月、3个月及6个月抽取外周静脉血,用双抗体夹心酶联免疫法(ELISA)检测血清中的髓过氧化物酶(MPO)及基质金属蛋白酶9(MMP-9),同时观察总胆固醇(TC)、三酰甘油(TG)、高密度脂蛋白胆固醇(HDL-C)、低密度脂蛋白胆固醇(LDL-C)、谷丙转氨酶(ALT)、总胆红素(BIL)、肌酸激酶(CK)、γ-谷氨酰转肽酶(γ-GGT)等指标,分别评估两组的抗炎作用、调脂疗效和不良反应及事件的发生率,分析其组间差异。结果序贯组和对照组的TC及LDL-C在治疗后均明显下降,差异有统计学意义(P<0.05)。研究比较发现,两组TC及LDL-C的在治疗后3 d均出现明显的下降趋势(下降幅度:TC 26.6%比14%;LDL-C 36.9%比19.4%),两组间比较差异有统计学意义(P<0.05)。在治疗1个月时,两组的TC及LDL-C进一步降低,其中LDL-C组间差异有统计学意义(45.0%比26.9%,P<0.05)在第3个月及第6个月时的差异仍具有统计学意义(P<0.05)。炎性指标:两组患者的MMP-9及MPO治疗后较治疗前相比,两者差异均有统计学意义(P<0.05)。序贯组的MPO在治疗后明显降低,与治疗前比较差异有统计学意义(F=18.455,P=0.000)。然而,MPO在治疗后两组间比较差异无统计学意义(P>0.05)。两组患者的MMP-9治疗后与治疗前比较,差异均有统计学意义(序贯组:F=46.911,P=0.000;对照组:F=19.156,P=0.000)。在治疗后3 d,序贯组和试验组MMP-9组间比较,差异有统计学意义(P<0.05);在治疗后1个月、3个月及6个月的差异均有统计学意义(P<0.05)。两组患者的不良反应及不良事件发生率比较,差异无统计学意义(P>0.05)。结论序贯治疗和常规治疗均可有效降低血脂,序贯治疗的降脂效果更强。两种疗法均能有效地抑制炎症因子,序贯治疗可更有效地抑制MMP-9,可能有利于进一步稳定斑块,防止其破裂。
关键词(KeyWords): 阿托伐他汀钙;序贯治疗;抗炎作用
基金项目(Foundation):
作者(Author): 王芍,张海涛,刘朝中
参考文献(References):
- [1]Paciaroni M,Bogousslavsky J.Statins and stroke prevention.Expert Rev Cardiovasc Ther,2009,7:1231-1243.
- [2]霍勇,葛均波,韩雅玲,等.急性冠状动脉综合征患者强化他汀治疗专家共识.中国介入心脏病学杂志,2014,22:4-6.
- [3]Ostadal P,Alan D,Hajek P,et al.The effect of early treatment by cerivastatin on the serum level of C-reactive protein,interleukin-6,and interleukin-8 in the patients with unstable angina and non-Qwave myocardial infarction.Mol Cell Biochem,2003,246:45-50.
- [4]刘健,王昭,王伟民.2012欧洲ST段抬高急性心肌梗死患者管理指南解读.中国医学前沿杂志(电子版),2013,5:55-60.
- [5]O'Gara PT,Kushner FG,Ascheim DD,et al.2013 ACCF/AHA Guideline for the Management of ST-Elevation Myocardial Infarction:A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines.J Am Coll Cardiol,2013,61:e78-e140.
- [6]Patti G,Pasceri V,Colonna G,et al.Atorvastain pretreatment improves outcomes in patients with acute coronary syndromes undergoing early percutaneous coronary intervention:results of the ARMYDA-ACS randomized trial.J Am Coll Cardiol,2007,49:1272-1278.
- [7]Vrints CJ.Pathophysiology of the no reflow phenomenon.Acute Card Care,2009,11:69-76.
- [8]Walter DH,Fichtlscherer S,Britten MB,et al.Benefi ts of immediate initiation of statin therapy following successful coronary stent implantation in patients with stable and unstable angina pectoris and Q-wave acute myocardial infarction.Am J Cardiol,2002,89:1-6.
- [9]HanPP,ChenYG,WangJL,et al.Meta-analysis of the role of high dose statins administered prior to percutaneous coronary intervention in reducing major adverse cardiac events in patients with coronary artery disease.Clln Exp Pharmacol Physid,2010,37:496-500.
- [10]Yu XL,Zhang HJ,Ren SD,et al.Effects of loading dose of atorvastatin before percutaneous coronary intervention on periprocedural myocardial injury.Coron Artery Dis,2011,22:87-91.
- [11]周滔,周胜华,祁述善,等.阿托伐他汀对单核细胞髓过氧化物酶和过氧化物增殖活化剂受体表达的影响.临床心血管病杂志,2007,23:59-61.
- [12]Liu C,Xie G,Huang W,et al.Elevated serum myeloperoxidase activities are signifi cantly associated with the prevalence of ACS and High LDL-C levels in CHD patients.J Atheroscler Thromb,2012,19:435-443.
- [13]Poderze A,Febbraio M,Sheibani N,et al.The macrophage scavenger receptor CD36 is the major receptor for LDL recogniton following modification by monocyte-generated reactive nitrogen species.J Clin Invest,2000,105:1095-1108.
- [14]Tang WH,Wu Y,Nicholls SJ,et al.Plasma Myeloperoxidase Predicts Incident Cardiovascular Risks in Stable Patients Undergoing Medical Management for Coronary Artery Disease.Clin Chem,2011,57:33-39.
- [15]Kulach A,Dabek J,Glogowska-Ligus J,et al.Effects of standard treatment on the dynamics of matrix metalloproteinases gene expression in patients with acute coronary syndromes.Pharmacol Rep,2010,62:1108-1116.
- [16]Luan Z,Chase AJ,Newby AC.Statins inhibit secretion of metalloprotei n-Asse-1,-2,-3,and-9 from vascular smooth muscle cells and macrophages.Arterioscler Thromb Vasc Biol,2003,23:769-775.
- [17]吴春芳,贺维亚.阿托伐他汀钙对急性脑梗死患者血清hs-CRP和MMP-9水平的影响.中国实用医刊,2013,40:59-60.
- [18]艾民,张清华,颜昌福,等.阿托伐他汀干预对急性心肌梗死患者血清IL-l8和MMP-9水平的影响.实用医学杂志,2013,29:105-107.
- [19]Pedersen TR,Faergeman O,Kastelein JJ,et al.High-dose atorvastatin vs usual-dose simvastatin for secondary prevention after myocardial infarction:the IDEAL study:a randomized controlled trial.JAMA,2005,294:2437-2445.
- [20]Reiner Z,Catapano AL,De Backer G,et al.ESC/EAS Guidelines for the management of dyslipidaemias:the Task Force for the management of dyslipidaemias of the European Society of Cardiology(ESC)and the European Atherosclerosis Society(EAS).Eur Heart J.2011,32:1769-1818.
- [21]Baigent C,Blackwell L,Emberson J,et al.Effi cacy and safety of more intensive low ering of LDL cholesterol:a mete-analysis of datea from 170 000 participants in 26 randomised trials.Lancet,2010,376:1670-1681.
- [22]Lee SW,Hau WK,Kong SL,et al.Virtual histology findings and effects of varying doses of atorvastatin on coronary plaque volume and composition in statin-naive patients:the VENUS study.Circ J,2012,76:2662-2672.
- [23]Sardella G,Lucisano L,Mancone M,et al.Comparison of high reloading RO suvastatin and Atorvastatin pretreatment in patients undergoing elective PCI to reduce the incidence of MyocArdial periprocedural necrosis.The ROMA II trial.Int J Cardiol,2013,168:3715-3720.
- [24]Newman C,Tsai J,Szarek M,et al.Comparative safety of atorvastatin 80 mg versus 10 mg derived from analysis of 49completed trials in 14,236 patients.Am J Cardiol,2006,97:61-67.
- [25]He GX,Tan W.High-dose atorvastatin pretreatment could diminishes microvascular impairment in patients undergoing elective percutaneous coronary intervention.J Geriatr Cardiol,2013,10:355-360.