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与将他汀类药物剂量加倍相比,依折麦布联合他汀类药物附加治疗或转换治疗实现目标血脂水平的一项汇总分析。

Achieving goal lipid levels with ezetimibe plus statin add-on or switch therapy compared with doubling the statin dose. A pooled analysis.

作者信息

Ambegaonkar Baishali M, Tipping Diane, Polis Adam B, Tomassini Joanne E, Tershakovec Andrew M

机构信息

Merck & Co., Inc., One Merck Drive, Whitehouse Station, NJ 07090, USA.

出版信息

Atherosclerosis. 2014 Dec;237(2):829-37. doi: 10.1016/j.atherosclerosis.2014.10.105. Epub 2014 Nov 4.

Abstract

OBJECTIVE

Evaluate the lipid-altering effects of ezetimibe added to ongoing statin therapy, statin titration, switching from statin monotherapy to a more potent statin or to ezetimibe/simvastatin.

METHODS

A pooled analysis of patient-level data from 17 double-blind, active or placebo-controlled studies of 8667 hypercholesterolemic adults randomized to ezetimibe 10 mg added to ongoing statins, statin titration (doubling), or switching from ongoing statins to rosuvastatin (10 mg) or to ezetimibe/simvastatin (10/20 and 40 mg). Percent change from baseline in low-density lipoprotein cholesterol (LDL-C) was estimated by analysis of variance. Percent of patients who achieved LDL-C and other guideline-recommended targets, and target lipid levels by baseline distance to goal were evaluated.

RESULTS

LDL-C percent change from baseline was -26.0 for ezetimibe added to ongoing statin therapy, -27.6 for switching from ongoing statin to ezetimibe/simvastatin, -19.7 for switching to rosuvastatin 10 mg, and -9.7 for dose doubling of the ongoing statin. For patients within 0.8 mmol/L (30 mg/dL) of the target at baseline, LDL-C target attainment rates were 75.9% for adding ezetimibe to ongoing statin, 72.8% for switching to ezetimibe/simvastatin, 61.8% for switching to rosuvastatin, and 44.3% for statin dose-doubling. Similarly, improvements in other lipids and achievement of non-high-density lipoprotein cholesterol and apolipoprotein B targets among this patient group were largest for ezetimibe added to ongoing statins and switching to ezetimibe/simvastatin; switching to rosuvastatin 10 mg and statin dose-doubling were less effective.

CONCLUSIONS

Adding ezetimibe to ongoing statin therapy appeared to be an effective option for patients who do not achieve lipid-lowering goals on statins alone.

摘要

目的

评估在正在进行的他汀类药物治疗基础上加用依折麦布、他汀类药物滴定、从他汀类单药治疗换用更强效的他汀类药物或依折麦布/辛伐他汀的调脂效果。

方法

对来自17项双盲、活性药物或安慰剂对照研究的患者水平数据进行汇总分析,这些研究涉及8667名高胆固醇血症成年人,他们被随机分配接受在正在进行的他汀类药物治疗基础上加用10毫克依折麦布、他汀类药物滴定(剂量加倍),或从正在进行的他汀类药物换用瑞舒伐他汀(10毫克)或依折麦布/辛伐他汀(10/20和40毫克)。通过方差分析估计低密度脂蛋白胆固醇(LDL-C)相对于基线的变化百分比。评估达到LDL-C和其他指南推荐目标的患者百分比,以及根据距目标的基线距离得出的目标血脂水平。

结果

在正在进行的他汀类药物治疗基础上加用依折麦布时,LDL-C相对于基线的变化百分比为-26.0;从正在进行的他汀类药物换用依折麦布/辛伐他汀时为-27.6;换用10毫克瑞舒伐他汀时为-19.7;正在进行的他汀类药物剂量加倍时为-9.7。对于基线时距目标在0.8毫摩尔/升(30毫克/分升)以内的患者,在正在进行的他汀类药物治疗基础上加用依折麦布时LDL-C目标达成率为75.9%,换用依折麦布/辛伐他汀时为72.8%,换用瑞舒伐他汀时为61.8%,他汀类药物剂量加倍时为44.3%。同样,在这组患者中,在正在进行的他汀类药物治疗基础上加用依折麦布和换用依折麦布/辛伐他汀时,其他血脂的改善以及非高密度脂蛋白胆固醇和载脂蛋白B目标的达成情况最为显著;换用10毫克瑞舒伐他汀和他汀类药物剂量加倍的效果较差。

结论

对于仅使用他汀类药物未达到降脂目标的患者,在正在进行的他汀类药物治疗基础上加用依折麦布似乎是一种有效的选择。

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