期刊文献+

不同强度阿托伐他汀对急性冠脉综合征患者高敏C反应蛋白的影响 被引量:3

Effects of atorvastatin with different doses on high-sensitivity C reactive protein's concentration in patients with acute coronary syndrome
在线阅读 下载PDF
导出
摘要 目的:研究不同强度阿托伐他汀对急性冠脉综合征(Acute coronary syndrome,ACS)患者高敏C反应蛋白(Highsensitivity C reactive protein,hs-CRP)的影响。方法:将2012年1月-2014年12月在遂宁市中心医院就诊的100例急性冠脉综合征患者和50例健康体检者分为阿托伐他汀中等强度组(20mg·d-1)、阿托伐他汀高强度组(40mg·d-1)和对照组,每组各50例,分别测定治疗前及治疗7天后急性冠脉综合征患者hs-CRP的浓度并进行比较分析。结果:治疗前ACS患者的hs-CRP的浓度显著高于对照组(P<0.05)。治疗7天后中等强度组和高强度组的hs-CRP较治疗前显著降低(P<0.05),并且高强度组较中等强度组的降低幅度更大(P<0.05)。但是两组治疗7天后的hs-CRP仍高于对照组(P<0.05)。结论:炎症反应贯穿ACS发展过程,阿托伐他汀明显降低ACS患者hs-CRP浓度,高强度阿托伐他汀更能显著抑制ACS的炎症反应。 Objective:To investigate the effect of atorvastatin with different doses on high-sensitivity C reactive protein(hsCRP)'s concentration in patients with acute coronary syndrome(ACS).Methods:One hundred patients with ACS and 50 health peoples in Suining Central Hospital from January 2012 to December 2014 were randomly divided into medium dose group(20mg·d-1atorvastatin),high dose group(40mg·d-1 atorvastatin)and control group.Concentration of plasma hs-CRP was detected and compared before treatment and after 7days treatment.Results:Concentration of plasma hs-CRP in ACS patients before treatment was notably higher than control group(P〈0.05).After 7days treatment,concentrations of plasma hs-CRP was decreased significantly in both medium dose group and high dose group(P〈0.05),and concentrations of plasma hs-CRP in high dose group decreased more significantly than medium dose group(P〈0.05).But concentrations of plasma hs-CRP in both medium dose group and high dose group after 7days treatment were still higher than control group(P〈0.05).Conclusions:The inflammatory reaction plays critical role in ACS.Atorvastatin can significantly decrease the concentration of plasma hs-CRP in patients with ACS.High dose atorvastatin can more notably suppress inflammatory reaction in ACS.
出处 《四川生理科学杂志》 2015年第3期118-120,共3页 Sichuan Journal of Physiological Sciences
关键词 冠状动脉疾病 炎症 C反应蛋白 阿托伐他汀 Coronary artery disease Inflammation C reactive protein Atorvastatin
  • 相关文献

参考文献9

  • 1Wasserman EJ, and Shipley NM. Atherothrombosis in acute coro- nary syndrome: mechanisms, markers, and mediators of vulnerabil- ity[J]. Mt Sinai J IVied, 2006, 73(1) : 431-439.
  • 2Ridker PM. High-sensitivity C-reactive protein: potential adjunct for global risk assessment in the primary prevention of cardiovascular disease[J]. Circulation, 2001, 103(13) : 1813-1818.
  • 3Thygesen K, Alpert JS, Jaffe AS, et al. Third universal definition of myocardial infarction[J]. J Am Coll Cardiol, 2012, 60(16) : 1581 -1598.
  • 4Shin J, Edelberg JE, Hong MK. Vulnerable atherosclerotic plaque: clinical implications[J]. Curt Vasc Pharrnacol, 2003, 1 (2): 183- 204.
  • 5Sugamura K, Ishii N, Weinberg AD. Therapeutic targeting of the effeetor T cell eo-stimulatory molecule OX40[J]. Nat Rev Immunol, 2004, 4(6): 420-431.
  • 6Higgins LM, McDonald SA, Whittle N, et al. Regulation of T cell activation in vitro and in vivo by targeting the OX40-OX40 ligand in- teraction: amelioration of ongoing inflammatory bowel disease with an OX40-IgG fusion protein, but not with an OX40 ligand-IgG fu- sion protein[J]. J Immunol, 1999, 162(1): 486-493.
  • 7高润霖.他汀类药物在急性冠状动脉综合征的应用[J].中华心血管病杂志,2003,31(8):635-636. 被引量:150
  • 8Rabar S, Harker M, O'Flynn N, et al. Lipid modification and car- diovascular risk assessment for the primary and secondary preven- tion of cardiovascular disease: summary of updated NICE guidance[J]. BMJ, 2014, 3491 g4356.
  • 9Jacobson TA, Ito MK, Maki KC, et al. National Lipid Association recommendations for patient-centered management of dyslDpidemia: part 1-executive summary[J]. J Clln Lipidol, 2014, 8(5): 473- 488.

共引文献149

同被引文献33

引证文献3

二级引证文献12

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