ApoA-I Event Reducing in Ischemic Syndromes II - AEGIS-II
Contribution To Literature:
Highlighted text has been updated as of September 13, 2024.
The AEGIS-II trial failed to show that CSL112 apoA-1 infusion reduces adverse CV outcomes after AMI.
Description:
The goal of the trial was to evaluate CSL112 apolipoprotein A-1 (apoA-1) infusion compared with placebo among patients with recent acute myocardial infarction (AMI). ApoA-1 increases cholesterol efflux capacity.
Study Design
- Randomized
- Parallel
- Blinded
- Placebo
- Stratified
Patients with recent AMI were randomized to CSL112 apoA-1 infusion, 4 infusions of 6 g (n = 9,112) vs. placebo (n = 9,107). The goal of CSL112 apoA-1 infusion is to improve high-density lipoprotein cholesterol (HDL-C) function and cholesterol efflux capacity.
- Total number of enrollees: 18,219
- Duration of follow-up: 12 months
- Mean patient age: 65.6 years
- Percentage female: 25.9%
- Percentage with diabetes: 68.7%
Inclusion criteria:
- AMI within the last 5 days
- ≥18 years of age
- Multivessel coronary disease and 1) diabetes, or 2) ≥65 years of age, prior MI, or peripheral arterial disease
Exclusion criteria:
- Hepatobiliary disease
- Hemodynamic instability
- Left ventricular ejection fraction <30%
- Estimated glomerular filtration rate <30 cc/min/1.73 m2
- Anticipated coronary artery bypass grafting
- Weight <50 kg (<110 lbs)
Other salient features/characteristics:
- Mean low-density lipoprotein cholesterol (LDL-C): 84 mg/dL
- Mean HDL-C: 9 mg/dL
Principal Findings:
The primary outcome (cardiovascular [CV] death, MI, or stroke) at 90 days was 4.8% in the CSL112 apoA-1 infusion group vs. 5.2% in the placebo group (p = 0.24). The findings were similar among tested subgroups.
Secondary outcomes:
- CV death, MI, or stroke at 365 days was 9.8% in the CSL112 apoA-1 infusion group vs. 10.5% in the placebo group (p = 0.14).
- Among patients with LDL-C ≥100 mg/dL, CV death, MI, or stroke at 365 days was 7.8% in the CSL112 apoA-1 infusion group vs. 9.9% in the placebo group (p = 0.006, p for interaction = 0.07).
Outcomes according to baseline LDL-C level:
- LDL-C ≥100 mg/dL: CSL112 was associated with a reduction in CV death, MI, or stroke vs. placebo at 12 months (hazard ratio [HR] 0.78, 95% confidence interval [CI] 0.65-0.93)
- LDL-C <100 mg/dL: CSL112 was not associated with a reduction in CV death, MI, or stroke vs. placebo at 12 months (HR 0.96, 95% CI 0.85-1.08)
Interpretation:
Among patients with AMI and multivessel disease with additional CV risk factors, 4 weekly infusions of CSL112 apoA-1 compared with placebo did not reduce major adverse CV events (CV death, MI, or stroke) through 90 days. The suggestion of benefit among those with elevated baseline LDL-C is hypothesis generating and deserves further evaluation.
References:
Gibson CM, Duffy D, Bahit MC, et al., for the AEGIS-II Committees and Investigators. Apolipoprotein A-I Infusions and Cardiovascular Outcomes in Acute Myocardial Infarction According to Baseline LDL-Cholesterol Levels: The AEGIS-II Trial. Eur Heart J 2024;Sep 2:[Epub ahead of print].
Gibson CM, Duffy D, Korjian S, et al., on behalf of the AEGIS-II Committees and Investigators. Apolipoprotein A1 Infusions and Cardiovascular Outcomes After Acute Myocardial Infarction. N Engl J Med 2024;390:1560-71.
Editorial: Ballantyne CM, Nambi V. HDL Therapeutics — Time for a Curtain Call or Time to Reconceptualize? N Engl J Med 2024;390:1622-3.
Povsic TJ, Korjian S, Bahit MC, et al., on behalf of the AEGIS-II Committees and Investigators. Effect of CSL112 on Recurrent Myocardial Infarction and Cardiovascular Death: Insights From the AEGIS-II Trial. J Am Coll Cardiol 2024;Apr 6:[Epub ahead of print].
Presented by Dr. C. Michael Gibson at the American College of Cardiology Annual Scientific Session (ACC.24), Atlanta, GA, April 6, 2024.
Clinical Topics: Acute Coronary Syndromes, Vascular Medicine
Keywords: ACC24, ACC Annual Scientific Session, Acute Coronary Syndrome, Myocardial Infarction, Novel Agents, Stroke
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