Key result
Alirocumab cuts MACE ~15% vs. placebo, independent of triglyceride lowering.
Why the study?
Does alirocumab reduce major adverse cardiovascular events in patients with recent acute coronary syndrome and elevated atherogenic lipoproteins on optimized statin therapy?
RCT (n=18,924)
Randomized
Does alirocumab reduce major adverse cardiovascular events in patients with recent acute coronary syndrome and elevated atherogenic lipoproteins on optimized statin therapy?
Hazard Ratio: 0.85 (95% CI 0.78–0.93)
While baseline triglyceride levels are associated with cardiovascular risk in ACS patients, the clinical benefit of alirocumab is not driven by its triglyceride-lowering effect.
It is unknown whether clinical benefit of proprotein convertase subtilisin/kexin type 9 inhibitors is associated with baseline or on-treatment triglyceride concentrations. This study sought to examine relations between triglyceride levels and the effect of alirocumab vs placebo on cardiovascular outcomes using prespecified and post hoc analyses of the ODYSSEY OUTCOMES (Evaluation of Cardiovascular Outcomes After an Acute Coronary Syndrome During Treatment With Alirocumab) trial. Patients with recent acute coronary syndrome (ACS) (n = 18,924) and elevated atherogenic lipoproteins despite optimized statin therapy were randomized to alirocumab 75 to 150 mg or matching placebo every 2 weeks subcutaneously. Major adverse cardiovascular events (MACE) were examined in relation to continuous or dichotomous triglyceride concentrations. Median baseline triglyceride concentration was 129 mg/dL. In both treatment groups, a 10-mg/dL higher baseline concentration was associated with an adjusted MACE HR of 1.008 (95% CI: 1.003-1.013; P < 0.005). Baseline triglycerides ≥150 vs <150 mg/dL were associated with a HR of 1.184 (95% CI: 1.080-1.297; P < 0.005). Versus placebo, alirocumab reduced low-density lipoprotein cholesterol from baseline (average, 54.7%) and reduced MACE (HR: 0.85; 95% CI: 0.78-0.93). At month 4, triglyceride levels were reduced from baseline by median 17.7 mg/dL (P < 0.001) and 0.9 mg/dL (P = NS) with alirocumab and placebo, respectively. A 10-mg/dL decline from baseline in triglycerides was associated with lower subsequent risk of MACE with placebo (HR: 0.988; 95% CI: 0.982-0.995; P < 0.005) but not with alirocumab (HR: 0.999; 95% CI: 0.987-1.010; P = 0.82). Among patients with recent ACS on optimized statin therapy, baseline triglycerides was associated with cardiovascular risk. However, the reduction in triglycerides with alirocumab did not contribute to its clinical benefit. (ODYSSEY Outcomes: Evaluation of Cardiovascular Outcomes After an Acute Coronary Syndrome During Treatment With Alirocumab; NCT01663402)
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Zahger et al. (2024) conducted an RCT in Acute coronary syndrome with elevated atherogenic lipoproteins (n=18,924). Alirocumab vs. Placebo was evaluated on Major adverse cardiovascular events (MACE) (HR 0.85, 95% CI 0.78-0.93). Alirocumab reduced MACE compared to placebo (HR 0.85; 95% CI 0.78-0.93), but the reduction in triglycerides with alirocumab did not contribute to this clinical benefit.
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