期刊文献+

阿托伐他汀对急性冠脉综合征患者血清基质金属蛋白酶-9的影响

The Atorvastatin Affect Serum Matrix Metalloproteinase-9 Level in Acute Coronary Syndrome Patients
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摘要 目的:观察急性冠脉综合征(ACS)患者经过阿托伐他汀治疗后其血清基质金属蛋白酶-9(MMP-9)的变化情况。方法:确诊为ACS患者90例为研究组,其中不稳定型心绞痛(UAP组)患者45例、急性心肌梗死(AMI组)患者45例入院后均在基础治疗的同时给予阿托伐他汀20 mg,每晚口服1次治疗,测定其治疗前后血清MMP-9水平。同时选取30例健康人为对照组,同样测定血清MMP-9水平。结果:研究组血清MMP-9水平明显高于对照组(P<0.01);治疗后,UAP组和AMI组血清MMP-9水平均比治疗前明显降低(P<0.01)。结论:阿托伐他汀能够明显降低ACS患者的血清MMP-9水平,在动脉粥样硬化斑块的稳定性方面可能发挥一定的作用。 Objective: To observe serum matrix metalloproteinase -9 ( MMP-9 ) level in the acute coronary syndrome ( ACS ) patients after atorvastatin therapy. Method: 90 ACS patients for the study group, unstable angina pectoris 45 cases ( UAP group ) and acute myocardial infarction 45 cases ( AMI group ), were admitted to hospital .except for the basic treatment, each patient was taken 20mg atorvastatin one day, and was measured the serum MMP-9 level before and after treatment. 30 patients healthy control group was measured serum MMP-9 level. Result: Study group serum MMP-9 levels was significantly higher than that in the control group ( P〈0.01 ) ; Both of the UAP group and AMI group serum level of MMP-9 was significantly lower than pretreatment ( P〈0.01 ) .Conclusion: Atorvastatin significantly reduces serum MMP-9 level in patients with ACS, and plays a role in atherosclerotic plaque stability.
出处 《中国医学创新》 CAS 2013年第31期15-17,共3页 Medical Innovation of China
关键词 基质金属蛋白酶-9 阿托伐他汀 急性冠脉综合征 Matrix metalloproteinase-9 Atorvastatin Acute coronary syndrome
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参考文献14

  • 1Rauch U, Osende J I, Chesebro J H.Statins and cardiovascular diseases: the mutiple .effects lipid-lowing therapy by statins[J]. Atherosclerosis, 2000, 153 ( 1 ) : 181-189.
  • 2Haroon Z A, Wannenburg T, Gupta M, et al.Localization of tissue transglutaminase in human carotid and coronary artery atherosclerosis: implications for plaque stability and progression[J].Laboratory investigation, 2001, 81 ( 1 ) : 83-93.
  • 3Riesen W F, Engler H, Risch M, et al.Short-term effects of atorvastatin on C-reactive protein[J].European heart journal, 2002, 23 ( 10) : 794-799.
  • 4Hansson G K.Immune mechanisms in atherosclerosis[J]. Arteriosclerosis, thrombosis, and vascular biology, 200 1, 21 (12): 1876-1890.
  • 5Dumont 0, Loufrani L, Henrion D.Key role of the NO pathway and matrix metalloprotease-9 in high blood flow induced remodeling of rat resistance arteries[J].Arterioscier Tbromb Vasc Bioi, 2007, 27 (2) : 317-324.
  • 6Kim S H, Kang Y J, Kim W J, et al.Tweak can induce proinflammatory cytokines and matrix metalloproteinase - 9 in macrophages[J].Cicr J, 2004, 68 (4) : 396-399.
  • 7Blankenberg S, Rupprecht H J, Poirier 0, et al.Plasma concentrations and genetic variation of matrix metalloproteinase 9 and prognosis of patients with cardiovascular disease[J].Circulation, 2003, 107 ( 12) : 1579-1585.
  • 8Fukumeto Y, Libby P, Rabkin E.Satins alter smooth muscle cell accumulation and collagen content in established a thermal of watanabeheritable hyperlipidemic rabbits[J].Circulation, 2001, 103 (7): 993.
  • 9Biasucci L M, Colizzi C, Rizzello V, et al.Role of inflammation in the pathogenesis of unstable coronary artery diseases[J].Scandinavian Journal of Clinical & Laboratory Investigation, 1999, 59 (230) : 12-22.
  • 10Tiefenbacher C P, Kapitza J, Dietz V, et al.Reduction of myocardial infarct size by fluvastatin[J].Am J Physiol Heart Cire Physio, 2003, 285 (3) : 59-64.

二级参考文献12

  • 1Brown BG,Zhao XQ.Importance of endothelial function in mediating the benefits of lipid-lowering therapy.Am J Cardiol,1998,82:49T-52T.
  • 2Williams JK,Sukhova GK,Herrington DM,et al.Pravastatin has cholesterol-lowering independent effects on the artery wall of atherosclerotic monkeys.J Am Coll Cardiol,1998,31:684-691.
  • 3Cannon CP,Braunwald E,McCabe CH,et aL Intensive versus moderato lipid lowering with statins after acute coronary syndromes.N Engl J Med,2004,350:1495-1504.
  • 4Waters DD,LaResa JC,Barter P,et al.Effects of high-dose atorvastatin on cerebrovaacular events in patients with stable coronary disease in the TNT (treating to now targets) study.J Am Coll Cardiol,2006,48:1793-1799.
  • 5The Scandinavian Simvnstatin Survival Study Group.Randomised trial of cholesterol lowering in 4444 patients with eoronary heart disease:the Scandinavian Simvastatin Survival Study (4S).Lancet,1994,344:1383-1389.
  • 6Piorkowski M,Fischer S,Stellbaum C,et al.Treatment with ezetimibe plus low-dose atorvastatin compared with higher-dose atorvastatin alone:is sufficient cholesterol-lowering enough to inhibit platclets? J Am Coil Cardio1,2007,49:1035-1042.
  • 7Loftus IM,Naylor AR,Goodail S,et al.Increased matrix metalloproteinase-9 activity in unstable carotid plaques.A potential role in acute plaque disruption.Stroke,2000,31:40-47.
  • 8Inoknho Y,Hanada H,Ishizaka H,et al.Plasma levels of matrix metalloprotoinase-9 and tissue inhibitor of mctalloproteinase-I are increased in the coronary circulation in patients with acute coronary syndrome.Am Heart J,2001,141:211-217.
  • 9Tziakas DN,Chalikias GK,Parissis JT,et al.Serum profiles of matrix metalloproteinases and their tissue inhibitor in patients with acute coronary syndromes.The effects of short-torm atorvastatin administration.Int J Cardiol,2004,94(2-3):269-277.
  • 10Crisby M,Nordin-Fredriksson C,Shah PK,et al.Pravastatin treatment increases collagen content and decreases lipid content,inflammation,mctalloproteinases,and cell death in human carotid plaques:implications for plaque stabilization.Circulation,2001,103:926-933.

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