期刊文献+

改良他汀序贯治疗对PCI术后斑块稳定性的影响 被引量:1

Effects of Modified Sequential Therapy Regimen with Atorvastatin on Postoperative Stability of Coronary Atherosclerotic Plaque after Percutaneous Coronary Intervention
原文传递
导出
摘要 目的评价改良的阿托伐他汀序贯治疗对经皮冠状动脉介入治疗(PCI)术患者血清高敏C反应蛋白(hs-CRP)、基质金属蛋白酶-9(MMP-9)及其内皮功能的影响。方法选取PCI患者100例随机分组:A组,PCI术前起始负荷量阿托伐他汀80 mg,后40 mg×7 d,以后20 mg qd;B组,PCI术前术后均每日阿托伐他汀20 mg。分别于服药前及术后24 h,服药后7 d分别测定hs-CRP、MMP-9及NO水平。同时观察药物不良反应及血管事件。结果服药前两组患者hs-CRP、MMP-9、NO水平比较差异无统计学意义,术后24 h,hs-CRP、MMP-9较术前升高,NO较术前降低(自身对比,P<0.05,组间对比,P>0.05);服药7 d后两组hs CRP及MMP-9均较术后24 h下降,NO较术后24 h升高(自身对比,P<0.05,组间对比,P<0.05)。结论改良阿托伐他汀序贯治疗可显著降低PCI术后体内炎症反应,稳定斑块,并改善内皮功能,并不增加肌溶解等不良事件发生。 Objective To assess the effects of modified sequential therapy regimen with atorvastatin on the serum hypersensitive C-reactive protein(hs-CRP),matrix metalloprotease-9(MMP-9) and endothelium function after percutaneous coronary intervention(PCI) in patients with coronary heart disease(CHD).Methods A total of 100 patients with CHD were randomly divided into two groups.In group A,80 mg of atorvastatin was given once time before PCI,and after PCI,40 mg/d×7 d,then 20 mg qd;in group B,20 mg/d of atorvastatin was given.Blood were taken at baseline,24 h and 7 day after PCI for serum hs-CRP,MMP-9 and NO tests.The major adverse cardiac events and drug side effect were observed.Results There was no significant difference in the level of serum hs-CRP,MMP-9 and NO at base(P0.05);24 hours after PCI,the level of hs-CRP and MMP-9 increased,while NO decreased(P0.05);7 d after taking atorvastatin,the level of hs-CRP and MMP-9 decreased while NO increased as compared to the value at 24 h after PCI(P0.05).Conclusion The modified sequential therapy regimen with atorvastatin can significantly reduce the inflammatory response in vivo after PCI,increase plaque stability,improve endothelial function and does not increase adverse events such as muscle dissolved.
出处 《中华全科医学》 2011年第12期1872-1872,1922,共2页 Chinese Journal of General Practice
关键词 阿托伐他汀 经皮冠状动脉介入治疗 高敏血清C反应蛋白 一氧化氮 基质金属蛋白酶9 Atorvastatin Percutaneous coronary intervention Hypersensitive C-reactive protein Nitric oxide Matrix metalloprotease-9
  • 相关文献

参考文献10

  • 1谢晓竞,杨解人,王安才.阿托伐他汀的降血压作用及其机制实验研究[J].中华全科医学,2008,6(9):882-884. 被引量:10
  • 2关英,陶莹,张微,李丽华.阿托伐他汀对冠心病患者血清细胞因子水平影响的研究[J].实用全科医学,2006,4(4):408-409. 被引量:11
  • 3Chitkara K, Pujara K. Drug-eluting Stents in Acute Coronary Syn- drome:Is There 'a Risk of Stent Thrombosis with Second-Generation Stents? [J]. Eur J Cardiovasc Med,2010,1 (2) :20-24.
  • 4Y'eh RW, Chandra M, McCulloch CE, et al. Accounting for the mortali- ty benefit of drug-eluting stents in percutaneous coronary intervention : a comparison of methods in a retrospective cohort study [ J ]. BMC Med,2011,9( 1 ) :78-80.
  • 5Emma Link, Sarah Parish, John Danesh, et al. C-reactive protein con- centration and the vascular benefits of statin therapy : an analysis of 20, 536 patients in the Heart Protection Study [ J ]. Lancet, 2011,377 (9764) :469-476.
  • 6Sakata K, Hamaoka K, Ozawa S, et al. Matrix metalloproteinase-9 in vascular lesions and endothelial regulation in Kawasakl disease [ J ]. Circ J,2010,74(8) :1670-1675.
  • 7Clearfield M. Statins and the primary prevention of cardiovascular e- vents [ J ]. Curr Atheroscler Rep,2006,8 ( 5 ) :390-396.
  • 8陶国华,金恒,吴红萍,赵刚.阿托伐他汀对慢性心衰sCD40L、BNP水平的影响[J].中华全科医学,2011,9(4):534-536. 被引量:12
  • 9Chien S. Effects of disturbed flow on endothelial cells [ J ]. Ann Biomed Eng,2008 ,36(4) :554-562.
  • 10Green D J, Jones H ,Thijssen D, et al. Flow-mediated dilation and car- diovascular event prediction: does nitric oxide matter? [ J ]. Hyper- tension ,2011,57 (3) :363-369.

二级参考文献21

  • 1Aukrust P, Gullestad L, Ueland T, et al. Inflammatory and anti-inflam- matory cytokines in chronic heart failure:potential therapeutic implica- tions [ J ]. Annals of Medicine,2005,37:74-85.
  • 2Mueller C, Laule-Kilian K, Christ A, et al. Inflammation and long-term mortality in acute congestive heart failure[ J]. American Heart Journal, 2006,151 (4) :845-850.
  • 3Gong KZ, Song G, Spiers JP, et al. Activation of immune and inflamma- tory systems in chronic heart failure:novel therapeutic approaches[ J]. International Journal of Clinical Practice, 2007,61 ( 4 ) : 611-621.
  • 4Thor Ueland, Pal Aukrust, Arne Yndestad, et al. Soluble CIMO ligand in acute and chronic heart failure[ J]. European Heart Journal,2005, 26(11) :1101-1107.
  • 5Heart Protection Study Collaborative Group. MRC/BHF Heart Protection Study of cholesterol lowering with simvastatin in 20,536 high-risk individuals : a randomised placebo-controlled trial [ J ]. Lancet, 2002, 360:7 -22.
  • 6Parissis JT, Nikolaou M, Farmakis D, et al. Clinical and prognostic im- plications of self-rating depression scales and plasma B-type nat riuret- ic peptide in hospitalized patients with chronic heart failure [ J ]. Heart, 2008,94(5 ) :585-589.
  • 7Cort6s R, Rivera M, Salvador A, et al. Urinary B-type natriuretic pep- tide levels in the diagnosis and prognosis of heart failure [ J ]. Journal of Cardiac FailUre,2007,13 (7) :549-555.
  • 8Nickenig G,Jung O,Strehlow K,et al.Hypercholesterolemia is associ-ated with enhanced angiotensin AT1-receptor expression[].American Journal of Physiology.1997
  • 9Wassmann S,Laufs U,Baumer AT,et al.Inhibition of geranylgeranyla-tion reduces angiotensinⅡ-mediated free radical production in vascu-lar smooth muscle cells:involvement of angiotensin AT1-receptor ex-pression an rac1GTPase[].Molecular Pharmacology.2001
  • 10Warnholtz A,Nickenig G,Schulz E,et al.Increased NADH-oxidase-mediated superoxide production in the early stages of atherosclerosis: evidence for involvement of the rennin-angiotensin system[].Circulation.1999

共引文献30

同被引文献11

  • 1聂绍平,蒋桔泉,曹林生,曾秋棠,杨光敏,薛毅,王祥.心肌内控制释放碱性成纤维细胞生长因子血管再生机制的探讨[J].临床心血管病杂志,2005,21(1):49-51. 被引量:3
  • 2Ohshima M, Yamaguchi Y, Kappert K, et al. bFGF rescues imatinib/ STI571-induced apoptosis of sis-NIH333 fibroblasts[ J]. Biochem Bio- phys Res Commun,2009,381 (2) :165-170.
  • 3O ' Driscoll C, Wallace D, Cotter TG. bFGF promotes photoreceptor cell survival in vitro by PKA-mediated inactivation of glycogen synthase ki- nase 3beta and CREB-dependent Bcl-2 up-regulation [ J ]. J Neuro- chem,2007,103 (3) :860-870.
  • 4Wang Y, Liu XC, Zhang GW, et al. A new transmyocardial degradable stent combined with growth factor, heparin, and stem cells in acute my- ocardial infarction [ J ]. Cardiovascular Research, 2009,84 ( 3 ) : 461- 469.
  • 5Xiao-Cheng Liu, Jian Zhao, Ying Wang. Heparin-and Basic Fibroblast Growth Factor-incorporated Stent:A New Promising Method for Myo- cardial Revascularization [ J ]. Journal of Surgical Research,2010,164 : 204-213.
  • 6Guang-Wei Zhang, Xiao-Cheng Liu, Yun Luan. Mechanisms of the pro- tective effects of BMSCs promoted by TMDR with heparinized bFGF- incorporated stent in pig model of acute myocardial ischemia [ J ]. J Cell Mol Med,2011,15 ( 5 ) : 1075-1086.
  • 7Mehmet A, Benjamin C, Frazier O, et al. Use of magnetic resonance imaging to assess myocardial perfusion after transmyocardiallaser re- vascularization [ J ]. The heart surgery forum,2009,12 (4) : E199-201.
  • 8Olsson R, Maxhuni A, Carlsson PO. Revascularization of transplanted pancreatic islets following culture with stimulators ofangiogenesis [ J ]. Transplantation, 2006,82 ( 3 ) :340-347.
  • 9Chang PY, Lu SC, Lee CM, et al. Homocysteine inhibits arterial endo- liethial cell growth through transcriptional downregulation of fibroblast growth factor-2 involving G protein and DNA methylation [ J ]. Circ Res,2008,102 (8) :933-941.
  • 10Iwakura A, Fujita M, Kataoka K, et al. Intramyocardial sustained de- livery of basic fibroblast growth factor improves angiogenesis and ven- tricular function in a rat infacrtion model [ J ]. Heart Vessels,2003,18 (4) :93-99.

引证文献1

二级引证文献5

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