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LDL-C 目标的实现取决于基线 LDL-C 以及他汀类药物的选择和剂量:来自 VOYAGER 数据库的分析。

Achievement of LDL-C goals depends on baseline LDL-C and choice and dose of statin: an analysis from the VOYAGER database.

机构信息

University of Keele, UK.

出版信息

Eur J Prev Cardiol. 2013 Dec;20(6):1080-7. doi: 10.1177/2047487313489875. Epub 2013 May 3.

DOI:10.1177/2047487313489875
PMID:23644489
Abstract

BACKGROUND

Reducing low-density lipoprotein cholesterol (LDL-C) levels decreases cardiovascular risk in direct proportion to the decrease in LDL-C.

DESIGN

The aim of this study was to assess the importance of baseline LDL-C and choice and dose of statin in achievement of LDL-C goals of 100 and 70 mg/dl, using a novel statistical model. The analysis included 30,102 patient exposures to rosuvastatin 10-40 mg or atorvastatin 10-80 mg from 31 direct comparative trials in the VOYAGER database.

METHODS

For each statin dose, percentage goal achievement was plotted for 20 equally large subgroups defined by baseline LDL-C. Logistic regression analysis was then performed for each statin dose to estimate the percentage of patients reaching target. Best-fit logistic regression curves were plotted 'pair-wise', comparing each rosuvastatin dose with equal or higher doses of atorvastatin.

RESULTS

LDL-C <100 mg/dl was achieved by 53.7-85.5% of patients on rosuvastatin 10-40 mg and 43.3-80.0% of those on atorvastatin 10-80 mg, whereas LDL-C <70 mg/dl was achieved by 4.5-44.0% of rosuvastatin-treated patients and 6.5-41.4% of those on atorvastatin. Similar differences in efficacy favouring rosuvastatin over equal or double doses of atorvastatin were observed across the range of baseline LDL-C levels for both LDL-C goals, being more pronounced at higher baseline values.

CONCLUSIONS

Baseline LDL-C and choice and dose of statin are important for LDL-C goal achievement. The present analysis may allow prediction of individual patient response to different statins at different doses.

摘要

背景

降低低密度脂蛋白胆固醇(LDL-C)水平与 LDL-C 的降低成正比,可降低心血管风险。

设计

本研究旨在使用新的统计模型评估基线 LDL-C 以及他汀类药物的选择和剂量对 LDL-C 目标值 100mg/dl 和 70mg/dl 的重要性。该分析包括 31 项直接比较试验中来自 VOYAGER 数据库的 30102 例患者接受瑞舒伐他汀 10-40mg 或阿托伐他汀 10-80mg 的暴露情况。

方法

对于每个他汀类药物剂量,根据基线 LDL-C 将 20 个相等大小的亚组绘制为百分比目标实现图。然后,对每个他汀类药物剂量进行逻辑回归分析,以估计达到目标的患者比例。绘制最佳拟合逻辑回归曲线“两两”比较,比较每个瑞舒伐他汀剂量与相等或更高剂量的阿托伐他汀。

结果

瑞舒伐他汀 10-40mg 治疗的患者中 LDL-C<100mg/dl 的比例为 53.7-85.5%,而阿托伐他汀 10-80mg 治疗的患者中为 43.3-80.0%;瑞舒伐他汀治疗的患者中 LDL-C<70mg/dl 的比例为 4.5-44.0%,而阿托伐他汀治疗的患者中为 6.5-41.4%。对于两个 LDL-C 目标值,在整个基线 LDL-C 范围内,都观察到了瑞舒伐他汀优于同等或双倍剂量阿托伐他汀的疗效差异,在较高的基线值时更为明显。

结论

基线 LDL-C 以及他汀类药物的选择和剂量对 LDL-C 目标的实现很重要。本分析可能允许预测不同剂量的不同他汀类药物对个体患者的反应。

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