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依折麦布/辛伐他汀与缓释烟酸联合给药对IIa型或IIb型高脂血症患者的血脂调节疗效及安全性

Lipid-altering efficacy and safety of ezetimibe/simvastatin coadministered with extended-release niacin in patients with type IIa or type IIb hyperlipidemia.

作者信息

Guyton John R, Brown B Greg, Fazio Sergio, Polis Adam, Tomassini Joanne E, Tershakovec Andrew M

机构信息

Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

J Am Coll Cardiol. 2008 Apr 22;51(16):1564-72. doi: 10.1016/j.jacc.2008.03.003.

Abstract

OBJECTIVES

This study evaluated the safety and lipid-altering efficacy of ezetimibe/simvastatin (E/S) coadministered with extended-release niacin (N) in patients with type IIa or IIb hyperlipidemia.

BACKGROUND

Current guidelines recommend consideration of combination drug therapy to achieve optimal low-density lipoprotein cholesterol (LDL-C) lowering and broader lipid-altering effects when treating hypercholesterolemic patients at high risk for atherosclerotic cardiovascular events.

METHODS

In this 24-week multicenter, randomized, double-blind study, 1,220 type IIa or IIb hyperlipidemic patients were randomized to treatment with E/S (10/20 mg/day) + N (titrated to 2 g/day), or N (titrated to 2 g/day), or E/S (10/20 mg/day). Changes from baseline in LDL-C (primary) and other secondary variables were assessed in the completers and modified intent-to-treat populations.

RESULTS

Coadministered E/S with N resulted in significantly greater reductions in LDL-C, non-high-density lipoprotein cholesterol, triglycerides, apolipoprotein B, and lipid/lipoprotein ratios, compared with either agent alone (p < 0.001). The combination increased levels of apolipoprotein A-I and high-density lipoprotein cholesterol significantly more than E/S (p < 0.001), and reduced high-sensitivity C-reactive protein levels significantly more than N (p = 0.005). A significantly greater percentage of patients discontinued the study in the N (25.0%) and N + E/S (23.3%) groups, compared with E/S (9.6%, p < 0.001) because of clinical adverse experiences (primarily flushing). Incidences of other clinical and laboratory adverse experiences (liver-, muscle-, and gastrointestinal-related) were similar for all groups.

CONCLUSIONS

Combination treatment with E/S plus N showed superior lipid-altering efficacy compared with N or E/S in type IIa or IIb hyperlipidemia patients and was generally well tolerated aside from N-associated flushing. This combination offers an effective, broad, lipid-altering therapy with improvements in lipid effects beyond LDL-C in these patients. (To Evaluate Ezetimibe/Simvastatin and Niacin [Extended Release Tablet] in Patients With High Cholesterol.

摘要

目的

本研究评估了依折麦布/辛伐他汀(E/S)与缓释烟酸(N)联合应用于IIa或IIb型高脂血症患者的安全性和调脂疗效。

背景

当前指南建议,在治疗具有动脉粥样硬化性心血管事件高风险的高胆固醇血症患者时,考虑联合药物治疗以实现最佳的低密度脂蛋白胆固醇(LDL-C)降低和更广泛的调脂效果。

方法

在这项为期24周的多中心、随机、双盲研究中,1220例IIa或IIb型高脂血症患者被随机分配接受E/S(10/20毫克/天)+ N(滴定至2克/天)、或N(滴定至2克/天)、或E/S(10/20毫克/天)治疗。在完成治疗者和改良意向性治疗人群中评估LDL-C(主要指标)和其他次要变量相对于基线的变化。

结果

与单独使用任何一种药物相比,E/S与N联合使用导致LDL-C、非高密度脂蛋白胆固醇、甘油三酯、载脂蛋白B以及脂质/脂蛋白比率的降低幅度显著更大(p < 0.001)。联合用药使载脂蛋白A-I和高密度脂蛋白胆固醇水平的升高幅度显著大于E/S(p < 0.001),且使高敏C反应蛋白水平的降低幅度显著大于N(p = 0.005)。由于临床不良事件(主要是潮红),N组(25.0%)和N + E/S组(23.3%)中止研究的患者百分比显著高于E/S组(9.6%,p < 0.001)。所有组的其他临床和实验室不良事件(与肝脏、肌肉和胃肠道相关)发生率相似。

结论

在IIa或IIb型高脂血症患者中,E/S加N的联合治疗显示出优于N或E/S的调脂疗效,除了与N相关的潮红外,总体耐受性良好。这种联合治疗提供了一种有效、广泛的调脂疗法,在这些患者中除了降低LDL-C外,还改善了脂质效应。(评估依折麦布/辛伐他汀和烟酸[缓释片]治疗高胆固醇血症患者的疗效)

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