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阿托伐他汀对急性冠脉综合征患者hs-CRP和IL-6的影响
引用本文:戴增斌,孟明,张文博,葛小丽. 阿托伐他汀对急性冠脉综合征患者hs-CRP和IL-6的影响[J]. 河北职工医学院学报, 2012, 0(4): 13-16
作者姓名:戴增斌  孟明  张文博  葛小丽
作者单位:1. 河北大学医学部,河北保定071000
2. 东方地球物理公司职工中心医院,河北徐水072555
摘    要:目的探讨阿托伐他汀对急性冠脉综合征(ACS)患者高敏C反应蛋白(hs-CRP)和白细胞介素-6(IL-6)的影响。方法 86例ACS患者随机分为2组,治疗组(46例)予常规药物治疗+阿托伐他汀20 mg/d,对照组(40例)仅予以常规治疗,随访1个月。在入选时及观察结束后检测丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)、肌酸激酶(CK)、hs-CRP及IL-6。结果经1个月治疗后,两组患者治疗前后AST、ALT、CK差异无统计学意义(P〉0.05);对照组hs-CRP及IL-6较治疗前有所降低(P〈0.05);治疗组hs-CRP及IL-6较治疗前显著降低(P〈0.01);与对照组比较,治疗后治疗组hs-CRP及IL-6均有所降低(P〈0.01)。结论阿托伐他汀可以降低ACS患者hs-CRP及IL-6水平,抑制冠状动脉粥样斑块的炎症反应。

关 键 词:阿托伐他汀  急性冠脉综合征  炎症

Effects of Atorvastatin on hs-CRP and IL-6 in patients with acute coronary syndrome
DAI Zengbin,MENG Ming,ZHANG Wenbo,GE Xiaoli. Effects of Atorvastatin on hs-CRP and IL-6 in patients with acute coronary syndrome[J]. Journal of Hebei Medical College for Continuing Education, 2012, 0(4): 13-16
Authors:DAI Zengbin  MENG Ming  ZHANG Wenbo  GE Xiaoli
Affiliation:1. Public Health Science Center of Hebei University, Baoding 071000, China 2. Central Hospital of Workers of Oriental Geophysics Company, Xushui 072555, China.)
Abstract:Objective To investigate the effects of Atorvastatin on hs-CRP and IL-6 in acute coronary syndrome. Methods 86 patients with ACS were divided randomly into statin group (n=46) and control group (n=40). Statin group received Atorvastatin (20rag/d) on the basis of conventional treatment of control group. The levers ofAST, ALT, CK, hs-CRP and IL-6 were detected before and after for 1 treatment months. Results There were no significant differences in the levels ofAST, ALT, and CK between the two groups before and after treatment (P〉0.05). After treatment the levels of hs-CRP and IL-6 in control group were significantly lower than that before treatment(P〈0.05). After treatment the levels of hs-CRP and IL-6 in statin group were significantly lower than that of control and before treatment(P〈0.01 and P〈0.001). Conclusion Atorvastatin can decrease hs-CRP and IL-6 levels in patients with ACS, which contributes to suppression of inflammation response.
Keywords:Atorvastatin  ACS  inflammation
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