Key result
Evolocumab reduces 3P-major cardiovascular events risk ~29% in patients with high-risk diabetes.
Why the study?
Does evolocumab reduce cardiovascular events in patients with high-risk diabetes without prior MI or stroke?
RCT (n=6,002)
Randomized
Does evolocumab reduce cardiovascular events in patients with high-risk diabetes without prior MI or stroke?
Answers are grounded in this paper and cite their sources.
Evolocumab significantly reduces the risk of major adverse cardiovascular events in patients with high-risk diabetes without prior MI or stroke, regardless of background cardioprotective therapies.
OBJECTIVE This prespecified analysis of Effect of Evolocumab in Patients at High Cardiovascular Risk Without Prior Myocardial Infarction or Stroke (VESALIUS-CV) evaluated the efficacy of the PCSK9 inhibitor evolocumab for preventing first cardiovascular events in patients with high-risk diabetes. RESEARCH DESIGN AND METHODS VESALIUS-CV randomized patients with high-risk diabetes (microvascular disease, insulin use, or duration ≥10 years) or qualifying atherosclerosis, but no prior myocardial infarction (MI) or stroke, and LDL cholesterol (LDL-C) ≥90 mg/dL to evolocumab 140 mg or matching placebo every 2 weeks. The dual primary end points were a composite of coronary heart disease death, MI or ischemic stroke (three-point major adverse cardiovascular event [3P-MACE]) and 3P-MACE plus ischemia-driven arterial revascularization (four-point [4P]-MACE). RESULTS Of the 6,002 patients with high-risk diabetes, 67% were on a high-intensity statin and 24% were on an sodium–glucose cotransporter 2 inhibitor (SGLT2i) or a glucagon-like peptide 1 receptor agonist (GLP-1RA) at baseline. The median LDL-C at 48 weeks was 47 mg/dL and 109 mg/dL in the evolocumab and placebo arms, respectively (P < 0.0001). After a median follow-up of 4.6 years, evolocumab decreased the relative rates of 3P-MACE and 4P-MACE by 29% (hazard ratio [HR] 0.71; 95% CI 0.59, 0.86; P = 0.0004) and 21% (HR 0.79; 95% CI 0.69, 0.91; P = 0.0013), respectively. These findings were consistent regardless of the presence or absence of qualifying atherosclerosis, baseline LDL-C, statin intensity, and SGLT2i or GLP-1RA use (Pint > 0.05 for each). The porportion of patients with all-cause death was 8.8% vs. 11.0% in the evolocumab versus placebo arms (HR 0.79; 95% CI 0.67, 0.93). CONCLUSIONS Evolocumab reduced the rate of cardiovascular events in patients with high-risk diabetes, regardless of the presence or absence of qualifying atherosclerosis and background use of other cardioprotective agents.
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Leiter et al. (2026) conducted an RCT in High-risk diabetes (n=6,002). Evolocumab vs. Placebo was evaluated on Composite of coronary heart disease death, MI or ischemic stroke (3P-MACE) and 3P-MACE plus ischemia-driven arterial revascularization (4P-MACE) (HR 0.71, 95% CI 0.59, 0.86, p=0.0004). Evolocumab reduced the risk of 3P-major cardiovascular events and 4P-major cardiovascular events in patients with high-risk diabetes over 4.6 years.
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