Rosuvastatin and atorvastatin in patients with acute coronary syndromes: head-to-head comparison of lipid-lowering and anti-inflammatory effects

P. Caravelli, E. Orsini, R. Pedrinelli, L. Bertini, Enrico Calogero, M. Marzilli
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Abstract

Background. Hypercholesterolemia and inflammation both contribute to the pathogenesis of atherosclerosis and its clinical manifestations. Statins, possessing both lipid-lowering and anti-inflammatory properties, are currently recommended in all ischemic syndromes. Purpose. To compare the effects of atorvastatin and rosuvastatin on lipid and inflammatory markers in patients with acute coronary syndromes (ACS). Methods. Two hundred thirty-nine consecutive patients with ACS, without familial hypercholesterolaemia and no statin treatment in the preceding 4 weeks, were randomly assigned within 24 hours after hospital admission to either atorvastatin 80 mg (119 patients) or rosuvastatin 20 mg (120 patients). Lipid and inflammatory markers were assessed before randomization and after 4 and 12 weeks of treatment. Results. Both statins similarly reduced total cholesterol and LDL-cholesterol at 4 weeks, with substantial stability at 12 weeks. At 4 weeks, LDL-cholesterol decreased from 129 mg/dL to 71 mg/dL in atorvastatin group and from 126 mg/dL to 71 mg/dL in rosuvastatin group. Apolipoprotein B significantly decreased in both groups. Otherwise, apolipoprotein A1 increased in rosuvastatin group only. As a consequence, ApoB/ApoA1 ratio decreased more in rosuvastatin group. No significant differences were seen in triglycerides, HDL-cholesterol and Lipoprotein (a) levels. Among inflammatory markers, hs-CRP, interleukin-6, interleukin 1-RA, TGF-β1, and MMP-9 significantly and similarly decreased at 4 and 12 weeks in both groups. Interleukin-10 levels decreased only in patients randomized to atorvastatin. Conclusions. A moderate dose of rosuvastatin provided similar effects, as compared to a high dose of atorvastatin, on a large series of lipid and inflammatory markers. Rosuvastatin was more effective than atorvastatin in reducing ApoB/ApoA1. Considering these findings, rosuvastatin 20 mg daily may be an alternative to atorvastatin 80 mg in acute coronary syndromes.
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瑞舒伐他汀和阿托伐他汀在急性冠状动脉综合征患者中的降脂和抗炎作用的正面比较
背景。高胆固醇血症和炎症都与动脉粥样硬化的发病机制和临床表现有关。他汀类药物具有降脂和抗炎特性,目前被推荐用于所有缺血性综合征。目的。比较阿托伐他汀和瑞舒伐他汀对急性冠脉综合征(ACS)患者血脂和炎症指标的影响。方法。239例ACS患者,无家族性高胆固醇血症且在入院前4周未接受他汀类药物治疗,在入院后24小时内随机分配到阿托伐他汀80 mg(119例)或瑞舒伐他汀20 mg(120例)组。在随机分组前和治疗4周和12周后评估脂质和炎症标志物。结果。两种他汀类药物在4周时同样降低了总胆固醇和低密度脂蛋白胆固醇,在12周时基本稳定。4周时,阿托伐他汀组ldl -胆固醇从129 mg/dL降至71 mg/dL,瑞舒伐他汀组从126 mg/dL降至71 mg/dL。两组载脂蛋白B均显著降低。此外,载脂蛋白A1仅在瑞舒伐他汀组升高。因此,瑞舒伐他汀组ApoB/ApoA1比值下降更多。甘油三酯、高密度脂蛋白胆固醇和脂蛋白(a)水平无显著差异。炎症标志物中,两组hs-CRP、白细胞介素-6、白细胞介素- 1-RA、TGF-β1和MMP-9在第4周和第12周均明显下降。白细胞介素-10水平仅在随机接受阿托伐他汀治疗的患者中下降。结论。与高剂量的阿托伐他汀相比,中等剂量的瑞舒伐他汀在一系列血脂和炎症标志物上提供了类似的效果。瑞舒伐他汀降低ApoB/ApoA1的效果优于阿托伐他汀。考虑到这些发现,瑞舒伐他汀20mg /天可能是急性冠状动脉综合征中阿托伐他汀80mg的替代方案。
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