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匹伐他汀在治疗老年原发性高胆固醇血症或混合性血脂异常患者时,在 12 周内的降脂疗效优于普伐他汀。

Pitavastatin shows greater lipid-lowering efficacy over 12 weeks than pravastatin in elderly patients with primary hypercholesterolaemia or combined (mixed) dyslipidaemia.

机构信息

Department of Clinical Biochemistry, Gentofte University Hospital, University of Copenhagen, Hellerup, Denmark.

出版信息

Eur J Prev Cardiol. 2013 Feb;20(1):40-53. doi: 10.1177/2047487312451251. Epub 2012 Jun 7.

Abstract

AIM

To compare the safety and efficacy of once-daily pitavastatin (1, 2, and 4 mg) and pravastatin (10, 20, and 40 mg) in elderly patients (≥ 65 years of age) with primary hypercholesterolaemia or combined (mixed) dyslipidaemia.

DESIGN

After a 6-8-week washout/dietary period, patients were randomized to six treatment groups (1, 2, or 4 mg pitavastatin vs. 10, 20, or 40 mg pravastatin) in a 12-week multicentre double-blind study. Patients (n = 942; men, 44.3%; Caucasian, 99.3%; mean age, 70 years; age range, 65-89 years) in all groups were well matched for duration of disease and diagnosis.

RESULTS

Mean decreases in low-density lipoprotein cholesterol over 12 weeks were 31.4-44.3% with pitavastatin 1-4 mg and 22.4-34.0% with pravastatin 10-40 mg (p < 0.001 for all dose comparisons). Compared with pravastatin, pitavastatin provided greater decreases in total cholesterol and apolipoprotein B in all dose groups (p < 0.001) and triglycerides in the low-dose (p = 0.001) and higher-dose (p = 0.016) groups, and greater increases in high-density lipoprotein cholesterol in the intermediate-dose (p = 0.013) and higher-dose (p = 0.023) groups. The proportions of patients achieving the European Atherosclerosis Society target with pitavastatin and pravastatin, respectively, were: low doses, 59.9 and 37.9%; intermediate doses, 79.5 and 51.0%; higher doses, 88.1 and 65.7% (p < 0.001 for all comparisons). Both statins were well tolerated, with no reports of myopathy or rhabdomyolysis.

CONCLUSION

Pitavastatin provides superior efficacy and comparable tolerability to pravastatin in elderly patients.

摘要

目的

比较每日一次匹伐他汀(1、2 和 4mg)和普伐他汀(10、20 和 40mg)在患有原发性高胆固醇血症或混合性血脂异常的老年患者(≥65 岁)中的安全性和疗效。

设计

经过 6-8 周的洗脱/饮食期后,患者被随机分配到六个治疗组(1、2 或 4mg 匹伐他汀与 10、20 或 40mg 普伐他汀),进行为期 12 周的多中心双盲研究。所有组的患者(n=942;男性,44.3%;白种人,99.3%;平均年龄 70 岁;年龄范围 65-89 岁)在疾病持续时间和诊断方面均匹配良好。

结果

12 周内,匹伐他汀 1-4mg 组的低密度脂蛋白胆固醇平均降低 31.4-44.3%,普伐他汀 10-40mg 组降低 22.4-34.0%(所有剂量比较均 p<0.001)。与普伐他汀相比,匹伐他汀在所有剂量组中均能更大程度地降低总胆固醇和载脂蛋白 B(p<0.001),并在低剂量(p=0.001)和高剂量(p=0.016)组中降低甘油三酯,在中剂量(p=0.013)和高剂量(p=0.023)组中增加高密度脂蛋白胆固醇。分别使用匹伐他汀和普伐他汀达到欧洲动脉粥样硬化学会目标的患者比例为:低剂量组,59.9%和 37.9%;中剂量组,79.5%和 51.0%;高剂量组,88.1%和 65.7%(所有比较均 p<0.001)。两种他汀类药物均耐受良好,无肌病或横纹肌溶解的报告。

结论

匹伐他汀在老年患者中的疗效优于普伐他汀,且耐受性相当。

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