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匹伐他汀与阿托伐他汀治疗对动脉粥样硬化性心血管疾病高危高胆固醇血症患者的疗效比较

Outcome of pitavastatin versus atorvastatin therapy in patients with hypercholesterolemia at high risk for atherosclerotic cardiovascular disease.

作者信息

Moroi Masao, Nagayama Daiji, Hara Fumihiko, Saiki Atsuhito, Shimizu Kazuhiro, Takahashi Mao, Sato Naoko, Shiba Teruo, Sugimoto Hideki, Fujioka Toshiki, Chiba Tatsuo, Nishizawa Kosuke, Usui Shuki, Iwasaki Yasuo, Tatsuno Ichiro, Sugi Kaoru, Yamasaki Junichi, Yamamura Shigeo, Shirai Kohji

机构信息

Division of Cardiovascular Medicine (Ohashi), Department of Internal Medicine, Faculty of Medicine, Toho University, Tokyo, Japan.

Nagayama Clinic, Oyama City, Tochigi, Japan.

出版信息

Int J Cardiol. 2020 Apr 15;305:139-146. doi: 10.1016/j.ijcard.2020.01.006. Epub 2020 Jan 20.

Abstract

BACKGROUND

There has been no report about outcome of pitavastatin versus atorvastatin therapy in high-risk patients with hypercholesterolemia.

METHODS

Hypercholesterolemic patients with one or more risk factors for atherosclerotic diseases (n = 664, age = 65, male = 54%, diabetes = 76%, primary prevention = 74%) were randomized to receive pitavastatin 2 mg/day (n = 332) or atorvastatin 10 mg/day (n = 332). Follow-up period was 240 weeks. The primary end point was a composite of cardiovascular death, sudden death of unknown origin, nonfatal myocardial infarction, nonfatal stroke, transient ischemic attack, or heart failure requiring hospitalization. The secondary end point was a composite of the primary end point plus clinically indicated coronary revascularization for stable angina.

RESULTS

The mean low-density lipoprotein cholesterol (LDL-C) level at baseline was 149 mg/dL. The mean LDL-C levels at 1 year were 95 mg/dL in the pitavastatin group and 94 mg/dL in the atorvastatin group. There were no differences in LDL-C levels between both groups, however, pitavastatin significantly reduced the risk of the primary end point, compared to atorvastatin (pitavastatin = 2.9% and atorvastatin = 8.1%, HR, 0.366; 95% CI 0.170-0.787; P = 0.01 by multivariate Cox regression) as well as the risk of the secondary end point (pitavastatin = 4.5% and atorvastatin = 12.9%, HR = 0.350; 95%CI = 0.189-0.645, P = 0.001). The results for the primary and secondary end points were consistent across several prespecified subgroups. There were no differences in incidence of adverse events between the statins.

CONCLUSION

Pitavastatin therapy compared with atorvastatin more may prevent cardiovascular events in hypercholesterolemic patients with one or more risk factors for atherosclerotic diseases despite similar effects on LDL-C levels.

摘要

背景

关于匹伐他汀与阿托伐他汀治疗高危高胆固醇血症患者的疗效,尚无相关报道。

方法

将患有一种或多种动脉粥样硬化疾病危险因素的高胆固醇血症患者(n = 664,年龄65岁,男性占54%,糖尿病患者占76%,一级预防患者占74%)随机分为两组,分别接受每日2毫克匹伐他汀治疗(n = 332)或每日10毫克阿托伐他汀治疗(n = 332)。随访期为240周。主要终点是心血管死亡、不明原因猝死、非致命性心肌梗死、非致命性中风、短暂性脑缺血发作或需住院治疗的心力衰竭的复合终点。次要终点是主要终点加上因稳定型心绞痛进行临床指征性冠状动脉血运重建的复合终点。

结果

基线时低密度脂蛋白胆固醇(LDL-C)平均水平为149毫克/分升。1年时,匹伐他汀组LDL-C平均水平为95毫克/分升,阿托伐他汀组为94毫克/分升。两组LDL-C水平无差异,然而,与阿托伐他汀相比,匹伐他汀显著降低了主要终点风险(匹伐他汀组为2.9%,阿托伐他汀组为8.1%,风险比[HR]为0.366;95%置信区间[CI]为0.170 - 0.787;多因素Cox回归分析P = 0.01)以及次要终点风险(匹伐他汀组为4.5%,阿托伐他汀组为12.9%,HR = 0.350;95%CI = 0.189 - 0.645,P = 0.001)。在几个预先设定的亚组中,主要和次要终点的结果一致。两种他汀类药物不良事件发生率无差异。

结论

尽管匹伐他汀和阿托伐他汀对LDL-C水平的影响相似,但与阿托伐他汀相比,匹伐他汀治疗可能更能预防患有一种或多种动脉粥样硬化疾病危险因素的高胆固醇血症患者发生心血管事件。

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