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Effects of high versus low-dose atorvastatin on high sensitive C-reactive protein in acute coronary syndrome

机译:大剂量阿托伐他汀与小剂量阿托伐他汀对急性冠脉综合征高敏C反应蛋白的影响

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Background:Cardiovascular disease is the leading cause of mortality. The previous findings which suggest the reduction in C-reactive protein (CRP) levels by statin encouraged us to conduct the present study in which we tested the effects of atorvastatin, on levels of hs-CRP in a prospective randomised clinical trial study on patients with acute coronary syndrome.Materials and Methods:Present prospective randomised clinical trial study conducted on 180 patients who had developed coronary artery disease and presented in emergency departments of Educational-Medical centers of Tabriz University of Medical Sciences. The patients were divided randomly into two groups and then two therapeutic protocols were given to them. One group medicated by high-dose atorvastatin (40 mg) and the other group received low-dose atorvastatin (20 mg). All variables were collected by questionnaires and were analyzed.Results:There were 180 patients consisted of 34 females and 56 males in low-dose atorvastatin group (L-DA group), and 30 females and 60 males in high-dose atorvastatin group (H-DA group) (P = 0.533). In this study atorvastatin in high doses decreased hs-CRP levels about 40% and in low doses it only caused decrease of 13.3%, and significant correlation was observed between two groups (Paired Sample T-test) (P = 0.001). Also atorvastatin in high doses decreased LDL levels about 23% and in low doses it only decreased 10%, and significant correlation was observed between two groups (Paired Sample T-test) (P = 0.001). Atorvastatin in high doses decreased HDL levels about 9% and in low doses it only decreased 6%, and again significant correlation was observed between two groups (P = 0.009).Conclusion:The present study confirms the novel observation that atorvastatin therapy results in a significant reduction in hs-CRP levels.
机译:背景:心血管疾病是导致死亡的主要原因。以前的发现提示他汀类药物降低了C反应蛋白(CRP)水平,这鼓励我们开展本研究,在一项前瞻性随机临床试验中,我们测试了阿托伐他汀对hs-CRP水平的影响。材料与方法:现有的前瞻性随机临床试验研究是针对180例患有冠状动脉疾病并在大不里士医科大学教育医学中心急诊科就诊的患者进行的。将患者随机分为两组,然后给予两种治疗方案。一组用大剂量阿托伐他汀(40毫克)服药,另一组接受小剂量阿托伐他汀(20毫克)。结果:小剂量阿托伐他汀组(L-DA组)180例,其中女34例,男56例,大剂量阿托伐他汀组30例,男60例(H)。 -DA组)(P = 0.533)。在这项研究中,阿托伐他汀在高剂量时可降低hs-CRP水平约40%,在低剂量时仅可导致13.3%下降,并且观察到两组之间存在显着相关性(配对T检验)(P = 0.001)。同样,高剂量的阿托伐他汀可降低LDL水平约23%,低剂量时仅可降低10%,两组之间存在显着相关性(配对T检验)(P = 0.001)。大剂量阿托伐他汀可降低HDL水平约9%,而小剂量阿托伐他汀仅可降低6%,两组之间又存在显着相关性(P = 0.009)。结论:本研究证实了新发现:阿托伐他汀治疗导致hs-CRP水平显着降低。

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