4.4 Article

Effects of icosapent ethyl on lipoprotein particle concentration and size in statin-treated patients with persistent high triglycerides (the ANCHOR Study)

期刊

JOURNAL OF CLINICAL LIPIDOLOGY
卷 9, 期 3, 页码 377-383

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacl.2014.11.009

关键词

Apolipoprotein B; Eicosapentaenoic acid; High-density lipoproteins; Hypertriglyceridemia; Icosapent ethyl; Low-density lipoproteins; Omega-3 fatty acid; Statin; Triglycerides

资金

  1. Abbott
  2. Amarin Pharma Inc.
  3. Amgen
  4. AstraZeneca
  5. GlaxoSmithKline
  6. Merck
  7. Novartis
  8. Roche
  9. Sanofi-Synthelabo
  10. NIH
  11. ADA
  12. AHA
  13. Alere
  14. Ardea
  15. Boehringer Ingelheim
  16. Bristol-Myers Squibb
  17. California Raisin Board
  18. Catabasis
  19. Cymabay
  20. Eisai
  21. Elcelyx
  22. Eli Lilly
  23. Esperion
  24. Forest
  25. Gilead
  26. Given
  27. Hanmi
  28. Hisun
  29. High Point Pharmaceuticals LLC
  30. Hoffmann-La Roche
  31. Home Access
  32. Janssen
  33. Metabolex
  34. Nektar
  35. Novo Nordisk
  36. Omthera
  37. Orexigen
  38. Pfizer
  39. Pronova
  40. Regeneron
  41. Sanofi
  42. Takeda
  43. TIMI
  44. Transtech Pharma
  45. Trygg
  46. Vivus
  47. WPU Pharmaceutical

向作者/读者索取更多资源

BACKGROUND: Icosapent ethyl (IPE) is a high-purity prescription form of eicosapentaenoic acid ethyl ester approved at a dose of 4 g/day as an adjunct to diet to reduce triglyceride (TG) levels in adult patients with severe hypertriglyceridemia (TG >= 500 mg/dL). OBJECTIVE: In this prespecified exploratory analysis from the ANCHOR study of patients at high cardiovascular risk with TG >= 200 and <500 mg/dL despite statin control of low-density lipoprotein cholesterol, we assessed the effects of IPE on lipoprotein particle concentration and size and examined correlations of atherogenic particles with apolipoprotein B (ApoB). METHODS: Nuclear magnetic resonance spectroscopy was used to measure lipoprotein particle concentration and size. RESULTS: Compared with placebo (n = 211), IPE 4 g/day (n = 216) significantly reduced concentrations of: total (12.2%, P = .0002), large (46.4%, P < .0001), and medium (12.1%, P = .0068) very-low-density lipoprotein (VLDL) particles; total (7.7%, P = .0017) and small (13.5%, P < .0001) LDL particles; and total (7.4%, P < .0001) and large (31.0%, P < .0001) high-density lipoprotein particles. Atherogenic lipoprotein particles (total VLDL and total LDL) correlated with ApoB at baseline (R-2 = 0.57) and week 12 (R-2 = 0.65) as did total LDL particle concentration at baseline (R-2 = 0.53) and week 12 (R-2 = 0.59). Compared with placebo, IPE 4 g/day significantly reduced VLDL (7.7%, P < .0001) and high-density lipoprotein (1.2%, P = .0014) particle sizes with a modest but significant increase in LDL particle size (0.5%, P = .0031). CONCLUSIONS: Compared with placebo, treatment with WE 4 g/day for 12 weeks reduced key atherogenic lipoprotein particle concentrations. At both baseline and end of study, atherogenic lipoprotein concentrations correlated with ApoB. (C) 2015 National Lipid Association. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).

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