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    Icosapent ethyl, a pure EPA omega-3 fatty acid: Effects on lipoprotein particle concentration and size in patients with very high triglyceride levels (the MARINE

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    BACKGROUND: Icosapent ethyl (IPE; formerly AMR101) is a high-purity prescription form of eicosapentaenoic acid ethyl ester. In the MARINE study we evaluated the efficacy and safety of IPE in patients with very high triglycerides (TG; 500mg/dL)andpreviouslydemonstratedsignificantreductionsinTGlevelswithnosignificantincreasesinlowβˆ’densitylipoprotein(LDL)cholesterollevels.OBJECTIVES:Inthisfollowβˆ’up,exploratoryanalysis,wereporttheeffectsofIPEonlipoproteinparticleconcentrationandsize.METHODS:MARINEwasaphase3,multicenter,placeboβˆ’controlled,randomized,doubleβˆ’blind,12βˆ’weekstudy.Hypertriglyceridemicpatients(N5229)wererandomizedtothreetreatmentgroups:IPE4g/day,IPE2g/day,orplacebo.Lipoproteinparticleconcentrationsandsizesweremeasuredbynuclearmagneticresonancespectroscopy.RESULTS:Comparedwithplacebo,IPE4g/daysignificantlyreducedmedianconcentrationsoflargeveryβˆ’lowβˆ’densitylipoprotein(VLDL;227.9500 mg/dL) and previously demonstrated significant reductions in TG levels with no significant increases in low-density lipoprotein (LDL) cholesterol levels. OBJECTIVES: In this follow-up, exploratory analysis, we report the effects of IPE on lipoprotein particle concentration and size. METHODS: MARINE was a phase 3, multicenter, placebo-controlled, randomized, double-blind, 12-week study. Hypertriglyceridemic patients (N 5 229) were randomized to three treatment groups: IPE 4 g/day, IPE 2 g/day, or placebo. Lipoprotein particle concentrations and sizes were measured by nuclear magnetic resonance spectroscopy. RESULTS: Compared with placebo, IPE 4 g/day significantly reduced median concentrations of large very-low-density lipoprotein (VLDL; 227.9%; P 5 .0211), total LDL (216.3%; P 5 .0006), small LDL (225.6%; P , .0001), and total high-density lipoprotein (HDL; 27.4%; P 5 .0063) particles and reduced VLDL particle size (28.6%; P 5 .0017). In this patient population with TG 500 mg/dL, IPE did not significantly change the overall sizes of LDL or HDL particles. CONCLUSION: IPE 4 g/day significantly reduced large VLDL, total LDL, small LDL, and total HDL particle concentrations and VLDL particle size in patients with TG $500 mg/dL. Changes in VLDL particle concentration and size reflect the TG-lowering effects of eicosapentaenoic acid. The reduction in LDL particle concentration with IPE is novel among u-3 therapies and is consistent with the previously reported reduction in apolipoprotein B and lack of LDL-C increase with IPE in patients with very high TG levels. Clinical trial registration number: NCT01047683
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