4.6 Article

Effect of Evolocumab on Coronary Plaque Phenotype and Burden in Statin-Treated Patients Following Myocardial Infarction

Journal

JACC-CARDIOVASCULAR IMAGING
Volume 15, Issue 7, Pages 1308-1321

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jcmg.2022.03.002

Keywords

acute coronary syndromes; atherosclerosis; clinical trials; lipid lowering; PCSK9 inhibitor

Funding

  1. Amgen Inc.
  2. National Health and Medical Research Council of Australia
  3. AstraZeneca
  4. Amgen
  5. Anthera
  6. CSL Behring
  7. Cerenis
  8. Eli Lilly
  9. Esperion
  10. Resverlogix
  11. Novartis
  12. InfraReDx
  13. Sanofi-Regeneron
  14. Akcea
  15. Boehringer Ingelheim
  16. Kowa
  17. Merck
  18. Takeda
  19. Pfizer
  20. SanofiRegeneron
  21. Novo Nordisk
  22. AbbVie
  23. Medtronic
  24. MyoKardia
  25. Medicines Company
  26. Silence Therapeutics
  27. Orexigen
  28. Abbott
  29. Abiomed
  30. Bayer
  31. Bristol Myers Squibb
  32. Boston Scientific
  33. Biotronik
  34. Cardiovalve
  35. Edwards Lifesciences
  36. MedAlliance
  37. Polares
  38. Sinomed
  39. V-Wave
  40. Xeltis
  41. National Heart Foundation of Australia [FLF102056]
  42. National Health and Medical Research Council of Australia [CDF1161506]
  43. Abbott Vascular

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The study on the use of evolocumab in combination with statins for patients with non-ST-segment elevation myocardial infarction showed that it can improve plaque composition in coronary arteries, with a stabilizing and regressive effect.
BACKGROUND The proprotein convertase subtilisin kexin type-9 inhibitor evolocumab produced coronary atheroma regression in statin-treated patients. OBJECTIVES The purpose of this study was to determine the effect of evolocumab on optical coherence tomography (OCT) measures of plaque composition. METHODS Patients with a non-ST-segment elevation myocardial infarction were treated with monthly evolocumab 420 mg (n = 80) or placebo (n = 81) for 52 weeks. Patients underwent serial OCT and intravascular ultrasound imaging within a matched arterial segment of a nonculprit vessel. The primary analysis determined the change in the minimum fibrous cap thickness and maximum lipid arc throughout the imaged arterial segment. Additional analyses determined changes in OCT features in lipid-rich plaque regions and plaque burden. Safety and tolerability were evaluated. RESULTS Among treated patients (age 60.5 +/- 9.6 years; 28.6% women; low-density lipoprotein cholesterol [LDL-C], 141.3 +/- 33.1 mg/dL), 135 had evaluable imaging at follow-up. The evolocumab group achieved lower LDL-C levels (28.1 vs 87.2 mg/dL; P < 0.001). The evolocumab group demonstrated a greater increase in minimum fibrous cap thickness (+42.7 vs +21.5 mm; P = 0.015) and decrease in maximum lipid arc (-57.5 degrees vs.-31.4 degrees; P = 0.04) and macrophage index (-3.17 vs-1.45 mm; P = 0.04) throughout the arterial segment. Similar benefits of evolocumab were observed in lipid-rich plaque regions. Greater regression of percent atheroma volume was observed with evolocumab compared with placebo (-2.29% +/- 0.47% vs-0.61% +/- 0.46%; P = 0.009). The groups did not differ regarding changes in microchannels or calcium. CONCLUSIONS The combination of statin and evolocumab after a non-ST-segment elevation myocardial infarction produces favorable changes in coronary atherosclerosis consistent with stabilization and regression. This demonstrates a potential mechanism for the improved clinical outcomes observed achieving very low LDL-C levels following an acute coronary syndrome. (C) 2022 by the American College of Cardiology Foundation.

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