Efficacy and Safety of Eicosapentaenoic Acid Ethyl Ester (AMR101) Therapy in Statin-Treated Patients With Persistent High Triglycerides (from the ANCHOR Study)

被引:281
作者
Ballantyne, Christie M. [1 ,2 ]
Bays, Harold E. [3 ]
Kastelein, John J. [4 ]
Stein, Evan [5 ]
Isaacsohn, Jonathan L. [5 ]
Braeckman, Rene A. [6 ]
Soni, Paresh N. [6 ]
机构
[1] Baylor Coll Med, Houston, TX 77030 USA
[2] Methodist DeBakey Heart & Vasc Ctr, Houston, TX USA
[3] Louisville Metab & Atherosclerosis Res Ctr, Louisville, KY USA
[4] Univ Amsterdam, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
[5] Medpace, Cincinnati, OH USA
[6] Amarin Pharma Inc, Bedminster, NJ USA
基金
美国国家卫生研究院;
关键词
DOUBLE-BLIND; OMEGA-3-FATTY-ACIDS; CHOLESTEROL; EVENTS;
D O I
10.1016/j.amjcard.2012.05.031
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
AMR101 is an omega-3 fatty acid agent containing >= 96% pure icosapent-ethyl, the ethyl ester of eicosapentaenoic acid. The efficacy and safety of AMR101 were evaluated in this phase 3, multicenter, placebo-controlled, randomized, double-blinded, 12-week clinical trial (ANCHOR) in high-risk statin-treated patients with residually high triglyceride (TG) levels (>= 200 and <500 mg/dl) despite low-density lipoprotein (LDL) cholesterol control (>= 40 and <100 mg/dl). Patients (n = 702) on a stable diet were randomized to AMR101 4 or 2 g/day or placebo. The primary end point was median percent change in TG levels from baseline versus placebo at 12 weeks. AMR101 4 and 2 g/day significantly decreased TG levels by 21.5% (p <0.0001) and 10.1% (p = 0.0005), respectively, and non-high-density lipoprotein (non-FIDL) cholesterol by 13.6% (p <0.0001) and 5.5% (p = 0.0054), respectively. AMR101 4 g/day produced greater TG and non-HDL cholesterol decreases in patients with higher-efficacy statin regimens and greater TG decreases in patients with higher baseline TG levels. AMR101 4 g/day decreased LDL cholesterol by 6.2% (p = 0.0067) and decreased apolipoprotein B (9.3%), total cholesterol (12.0%), very-low-density lipoprotein cholesterol (24.4%), lipoprotein-associated phospholipase A(2) (19.0%), and high-sensitivity C-reactive protein (22.0%) versus placebo (p <0.001 for all comparisons). AMR101 was generally well tolerated, with safety profiles similar to placebo. In conclusion, AMR101 4 g/day significantly decreased median placebo-adjusted TG, non-HDL cholesterol, LDL cholesterol, apolipoprotein B, total cholesterol, very-low-density lipoprotein cholesterol, lipoprotein-associated phospholipase A2, and high-sensitivity C-reactive protein in statin-treated patients with residual TG elevations. (C) 2012 Elsevier Inc. All rights reserved. (Am J Cardiol 2012;110:984-992)
引用
收藏
页码:984 / 992
页数:9
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