期刊文献+

不同剂量辛伐他汀对急性冠状动脉综合征患者炎症因子的影响

Effects of different dose of simvastatin on plaque stability and eudothelial function in patients with acute coronary syndrome
下载PDF
导出
摘要 目的观察不同剂量辛伐他汀对急性冠状动脉综合征(ACS)患者血清高敏C一反应蛋白(hs-CRP)、内皮素-1(ET-1)及血脂的影响,探讨不同剂量辛伐他汀在血管内皮功能、斑块稳定性和炎症反应中的作用。方法选取临床确诊为ACS患者80例,均总胆固醇(TC)≥4.68mmol/L和(或)低密度脂蛋白胆固醇(LDL-C)≥2.6mmol/L,年龄52岁~75岁。入院48h内空腹采静脉血测定血脂等生化指标及hsCRP、ET-1,将患者随机分为20mg组(A组,40例)和40mg组(B组,40例),均为每晚服药1次,分别于用药前,用药后4、12周测定TC、LDL-C、高密度脂蛋白胆固醇(HDL-C)、甘油三脂(TG)及hsCRP、ET-1,随访3个月内所有不良反应,观察终点为6个月后心脏事件的发生率。结果(1)两组服药后4、12周后TC、LDL-C、hsCRP、ET-1水平均较治疗前明显降低(P<0.05),B组较A组降低更明显,P<0.05;(2)B组累及心脏事件发生率较A组明显减少(P<0.05);(3)两组均无严重不良反应。结论ACS患者应用辛伐他汀40mg/d,能更有效地降脂,提高达标率,明显抑制炎症因子,改善内皮功能,稳定粥样斑块,减少住院率及心脏血管事件的发生率,且安全、耐受性好。 Objectives To explore the effects of different dose of simvastatin on plaque stability and inflammatory reaction (such as the changes of high sensitive-C reaction protein (hsCRP), endothlin-1 (ET-1) and blood lipid) in patients with acute coronary syndrome. Method Eighty patients with ACS, age 52 to 75 years, the total cholesterol (TC) 〈4.68 mmol. L-1 and/or low-density lipoprotein(LDL) 〈2.6 mmol.L-1,were randomly divided into 2 groups: group A (n=40) gave simvastatin 20mg.d-1, group B (n=40) 40mg. d-1. The levels of blood triglycerides (TC), LDL, high-density lipoprotein (HDL), TG, and high sensititivity C-reactive protein(hsCRP), endothlin-1 (ET-1) were all detected before and after 1 month, 3 months of the treament. All adverse reaction in 3 months were followed up. The primary ending point is the incidence of the cardiovascular disease. Restult After 1 month or 3 months of the treatment, the levels of blood TC, LDL, HDL, TG, hsCRP and ET-1 in the two groups were decreased significantly than those before the treatment, especially in group B(P 〈0.05 (. During the follow-up the incidence of cardiac events in group B was less than that in group A markedly, ( P 〈 0.05 (. No severe adverce effects were found in the two groups. Conclusion Early treatment with sinmvastatin 40 mg.d-1 had a good effect on the lowering of blood lipid , inhibiting the product of inflammatory factors , ameliorating endothelial function and reducing the incidence of cardiac events , while it is safe for the patients with ACS.
出处 《实用心脑肺血管病杂志》 2008年第8期7-10,共4页 Practical Journal of Cardiac Cerebral Pneumal and Vascular Disease
关键词 急性冠状动脉综合征 辛伐他汀 C-反应蛋白 内皮素-1 Acute coronary syndrome Simvastatin C-reactive protein Endothelin-1
  • 相关文献

参考文献7

  • 1Kinlay S, Selwyn AP, Delagrange D, et al. Biological mechanisms for the clinical success of hpid-lowering in coronary artery disease and the use of surrogate end points [J]. Curr Opin Lipidol , 1996,7:389-397.
  • 2杨胜利,何作云,何秉贤.C-反应蛋白和急性冠脉综合征[J].中国急救医学,2003,23(9):641-642. 被引量:18
  • 3Alberolaaguilar A M,Revert F,Moya A, et al. Intravenous BQ-123 and phosphoramidon reduce ventricular ectopic beats and myocardial infarct size in dogs submitted to coronary occlusion and reperfusion [J]. Gen Pharmacol,2000,35:143-147.
  • 4Waters DD, Azar RR.Should intensive cholesterol lowering play a role in the management of acute coronary syndromes [J].Am J Cardiol,2000,86 (8B): 35J-42J.
  • 5Liuzzo G, Biasucci LM, Gallimore JR, et al. The prognostic value of C-reactive protein and serum amyloid-A ptrotein in severe unstable angina [J]. N Engl J Med, 1994,331:417-424.
  • 6王增武,满荣海,史平,武阳丰,陆宗良.他汀类药物预防心血管病事件的非调脂机制[J].心血管病学进展,2003,24(1):1-4. 被引量:63
  • 7Heart protection Study Collaborative Group.MRC/BHF Heart protection study of cholesterol loweringe with simvastatin in 20536 high-risk individuals : a randomized placebo-controlled trial [J], Lancet, 2002, 360:7-22.

二级参考文献23

  • 1Masexi A. Inflammation, atherosclerosis, and ischemie events-exploring the hidden side of the moon[l].N Engl J Med, 1997,336:1014-1016.
  • 2Kuller LH,Tracy RP, Shaten J, et al. Relation of C-reactive protein and coronary heart disease in the MRFIT nested case-control study[J]. Am J Epidemiol, 1996,144:537-547.
  • 3Anderson JL, Carlquist JF, Muhlestein JB, et al. Evaluation of C-reactive protein, an inflammation marker, and infections serology as risk factors for coronary artery disease and myocardial infaretion[J]. J Am Coll Cardiol,1998,32:35-41.
  • 4Rus H, Niculescu FI. Inflammation, aspirin, and the risk of cardiovascular disease[J]. N Engl J Med,1997,337:423.
  • 5Torzewski J, Torzewski M, Bowyer DE, et al. C-reactive protein frequently colocalizes with the terminal complement complex in the intima of early atherosclerotic lesions of human coronary arteries[J]. Arterioscler Thromb Vase Bid, 1998,18:1386-1392.
  • 6Ridker PM. High-sensitivity C-reactive protein: potential adjunct for global risk assessment in the primary prevention of cardiovascular disease[J]. Circulation,2001,103:1813-1818.
  • 7Haverkate F, Thompson SG, Pyke SDM, et al. Production of C-reactive protein and risk of coronary events in stable and unstable angina [J]. Lancet, 1997,349:462-466.
  • 8Ridker PM, Cushman M, Stampfer MJ, et al Inflammation, aspirin, and the risk of cardiovascular disease in apparently health men[J]. N Engl J Med, 1997,336:973-979.
  • 9Ahdelmouttaled I, Danchin N, Ilardo C, et al. C-reactive protein and coronary artery disease: additional evidence of the implication of an inflammatory process in acute coronary syndromes[J]. Am Heart J, 1999,137:346-351.
  • 10Marrow DA, Rifai N, Antman EM, et al . C reactive protein is a potent predictor of mortality independently of and in combination with troponin T in acute coronary syndromes: a TIMI 11 A substudy [J]. J Am Coll Cardiol, 1998,31 : 1460-1465.

共引文献79

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部