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首页> 外文期刊>American journal of cardiovascular drugs: drugs, devices, and other interventions >Icosapent ethyl, a pure ethyl ester of eicosapentaenoic acid: Effects on circulating markers of inflammation from the MARINE and ANCHOR studies
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Icosapent ethyl, a pure ethyl ester of eicosapentaenoic acid: Effects on circulating markers of inflammation from the MARINE and ANCHOR studies

机译:二十碳五烯酸乙酯,二十碳五烯酸的纯乙酯:对海洋和锚固研究的炎症循环标志物的影响

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Background: Icosapent ethyl (IPE) is a high-purity prescription form of eicosapentaenoic acid ethyl ester approved by the US Food and Drug Administration as an adjunct to diet to reduce triglyceride (TG) levels in adult patients with severe (≥500 mg/dL) hypertriglyceridemia. In addition to TG-lowering effects, IPE also reduces non-high-density lipoprotein cholesterol and apolipoprotein B levels without significantly increasing low-density lipoprotein cholesterol (LDL-C) in patients with very high TG levels ≥500 mg/dL (MARINE study) and in patients with well-controlled LDL-C and residually high TG levels 200-500 mg/dL (ANCHOR study). This analysis examined the effect of IPE on inflammatory markers in patients from MARINE and ANCHOR. Methods: MARINE (N = 229) and ANCHOR (N = 702) were Phase III, double-blind studies that randomized hypertriglyceridemic patients to IPE 4 g/day, 2 g/day, or placebo. This analysis assessed the median placebo-adjusted percentage change from baseline in markers representing various stages of atherosclerotic inflammation such as intercellular adhesion molecule-1 (ICAM-1), oxidized low-density lipoprotein (Ox-LDL), lipoprotein-associated phospholipase A2 (Lp-PLA2), interleukin-6 (IL-6), and high-sensitivity C-reactive protein (hsCRP). Results: Compared to placebo, IPE 4 g/day significantly decreased Ox-LDL (13 %, p 0.0001, ANCHOR), Lp-PLA2 (14 %, p 0.001, MARINE; 19 %, p 0.0001, ANCHOR), and hsCRP levels (36 %, p 0.01, MARINE; 22 %, p 0.001, ANCHOR), but did not significantly change ICAM-1 and IL-6 levels. In the MARINE study, IPE 2 g/day did not significantly change ICAM-1, Ox-LDL, Lp-PLA2, IL-6, or hsCRP levels. Also, compared to placebo in the ANCHOR study, IPE 2 g/day significantly decreased Lp-PLA 2 levels (8 %, p 0.0001), but did not significantly change levels of other assessed inflammatory markers. Conclusion: Compared to placebo, in hypertriglyceridemic patients, IPE 4 g/day significantly decreased Ox-LDL, Lp-PLA2, and hsCRP levels.
机译:背景:二十碳五烯酸乙酯(IPE)是二十碳五烯酸乙酯的高纯度处方形式,已被美国食品和药物管理局批准,可作为饮食的辅助剂,以降低重度(≥500mg / dL)成年患者的甘油三酸酯(TG)水平)高甘油三酯血症。除了降低TG的作用外,对于TG≥500 mg / dL很高的患者,IPE还可以降低非高密度脂蛋白胆固醇和载脂蛋白B水平,而不会显着增加低密度脂蛋白胆固醇(LDL-C)(MARINE研究),以及LDL-C受到良好控制且TG浓度持续高至200-500 mg / dL的患者(ANCHOR研究)。该分析检查了IPE对MARINE和ANCHOR患者炎症标记的影响。方法:MARINE(N = 229)和ANCHOR(N = 702)是III期双盲研究,将高甘油三酯血症患者IPE随机分为4 g /天,2 g /天或安慰剂。这项分析评估了代表动脉粥样硬化炎症各个阶段的标志物(例如细胞间粘附分子1(ICAM-1),氧化的低密度脂蛋白(Ox-LDL),脂蛋白相关的磷脂酶A2( Lp-PLA2),白介素6(IL-6)和高敏感性C反应蛋白(hsCRP)。结果:与安慰剂相比,IPE 4 g / day显着降低Ox-LDL(13%,p <0.0001,ANCHOR),Lp-PLA2(14%,p <0.001,MARINE; 19%,p <0.0001,ANCHOR),和hsCRP水平(36%,p <0.01,海洋; 22%,p <0.001,ANCHOR),但未显着改变ICAM-1和IL-6水平。在海洋研究中,每天2 g IPE不会显着改变ICAM-1,Ox-LDL,Lp-PLA2,IL-6或hsCRP水平。此外,与ANCHOR研究中的安慰剂相比,IPE 2 g /天可显着降低Lp-PLA 2水平(8%,p <0.0001),但不会显着改变其他评估的炎症标志物的水平。结论:与安慰剂相比,高甘油三酯血症患者IPE 4 g /天可显着降低Ox-LDL,Lp-PLA2和hsCRP水平。

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