Journal
JACC-CARDIOVASCULAR IMAGING
Volume 15, Issue 7, Pages 1308-1321Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.jcmg.2022.03.002
Keywords
acute coronary syndromes; atherosclerosis; clinical trials; lipid lowering; PCSK9 inhibitor
Funding
- Amgen Inc.
- National Health and Medical Research Council of Australia
- AstraZeneca
- Amgen
- Anthera
- CSL Behring
- Cerenis
- Eli Lilly
- Esperion
- Resverlogix
- Novartis
- InfraReDx
- Sanofi-Regeneron
- Akcea
- Boehringer Ingelheim
- Kowa
- Merck
- Takeda
- Pfizer
- SanofiRegeneron
- Novo Nordisk
- AbbVie
- Medtronic
- MyoKardia
- Medicines Company
- Silence Therapeutics
- Orexigen
- Abbott
- Abiomed
- Bayer
- Bristol Myers Squibb
- Boston Scientific
- Biotronik
- Cardiovalve
- Edwards Lifesciences
- MedAlliance
- Polares
- Sinomed
- V-Wave
- Xeltis
- National Heart Foundation of Australia [FLF102056]
- National Health and Medical Research Council of Australia [CDF1161506]
- 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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