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贝特类药物联合他汀类药物治疗混合性血脂异常患者的疗效和安全性:三项为期 12 周的 3 期随机对照研究的汇总分析。

Efficacy and safety of fenofibric acid in combination with a statin in patients with mixed dyslipidemia: Pooled analysis of three phase 3, 12-week randomized, controlled studies.

机构信息

Baylor College of Medicine, 6565 Fannin St. #A601, Houston, TX 77030 USA.

出版信息

J Clin Lipidol. 2009 Apr;3(2):125-37. doi: 10.1016/j.jacl.2009.02.007. Epub 2009 Feb 11.

Abstract

BACKGROUND

Patients with mixed dyslipidemia often require combination therapy to manage multiple lipid abnormalities.

OBJECTIVE

To evaluate fenofibric acid in combination with a statin across three studies of patients with mixed dyslipidemia.

METHODS

As prospectively planned, data were pooled from three randomized, double-blind, phase 3 studies of patients with low-density lipoprotein cholesterol (LDL-C) ≥130mg/dL, triglycerides (TG) ≥150mg/dL, and high-density lipoprotein cholesterol (HDL-C) <40mg/dL (men) or <50mg/dL (women). A total of 2715 patients were randomly assigned to 12-week treatment with fenofibric acid 135mg monotherapy; low-, moderate-, or high-dose statin (rosuvastatin, simvastatin, or atorvastatin, depending on study) monotherapy; or fenofibric acid + low- or moderate-dose statin. The primary efficacy comparisons were mean percent change in HDL-C and TG (combination therapy vs. statin) and LDL-C (combination therapy vs. fenofibric acid).

RESULTS

Fenofibric acid + low-dose statin increased HDL-C (18.1% vs. 7.4%) and reduced TG (-43.9% vs. -16.8%) versus low-dose statin monotherapy and reduced LDL-C (-33.1% vs. -5.1%) versus fenofibric acid monotherapy (P <.001 for all). Fenofibric acid + moderate-dose statin increased HDL-C (17.5% vs. 8.7%) and reduced TG (-42.0% vs. -23.7%) versus moderate-dose statin monotherapy and reduced LDL-C (-34.6% vs. -5.1%) versus fenofibric acid monotherapy (P <.001 for all). Combination therapy was generally well tolerated, and safety profiles were similar to monotherapies. No rhabdomyolysis was reported.

CONCLUSION

In patients with mixed dyslipidemia, combination therapy simultaneously improved multiple lipid abnormalities more effectively than fenofibric acid or statin monotherapies.

摘要

背景

患有混合性血脂异常的患者通常需要联合治疗来控制多种脂质异常。

目的

评估在三项混合性血脂异常患者的研究中,使用非诺贝特酸联合他汀类药物的效果。

方法

根据预先计划,对三项随机、双盲、3 期研究中患有低密度脂蛋白胆固醇(LDL-C)≥130mg/dL、甘油三酯(TG)≥150mg/dL 和高密度脂蛋白胆固醇(HDL-C)<40mg/dL(男性)或<50mg/dL(女性)的患者的数据进行了汇总。共 2715 例患者被随机分配至 12 周的治疗期,接受非诺贝特酸 135mg 单药治疗;低、中或高剂量他汀(依研究而定,为瑞舒伐他汀、辛伐他汀或阿托伐他汀)单药治疗;或非诺贝特酸+低或中剂量他汀。主要疗效比较为 HDL-C 和 TG(联合治疗与他汀类药物)及 LDL-C(联合治疗与非诺贝特酸)的平均百分比变化。

结果

与低剂量他汀类药物单药治疗相比,非诺贝特酸+低剂量他汀治疗使 HDL-C 增加(18.1% vs. 7.4%)和 TG 降低(-43.9% vs. -16.8%),使 LDL-C 降低(-33.1% vs. -5.1%);与非诺贝特酸单药治疗相比,非诺贝特酸+中剂量他汀治疗使 HDL-C 增加(17.5% vs. 8.7%)和 TG 降低(-42.0% vs. -23.7%),使 LDL-C 降低(-34.6% vs. -5.1%)(所有比较均<.001)。联合治疗通常具有良好的耐受性,且安全性与单药治疗相似。未报告横纹肌溶解症。

结论

在患有混合性血脂异常的患者中,与非诺贝特酸或他汀类药物单药治疗相比,联合治疗更有效地同时改善多种脂质异常。

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