Bempedoic acid vs ezetimibe added to statin therapy: Cardiovascular outcomes in the real-world-The BEYOND-REAL Study

Scritto il 12/03/2026
da Raechel T White

J Clin Lipidol. 2026 Feb 20:S1933-2874(26)00047-4. doi: 10.1016/j.jacl.2026.02.014. Online ahead of print.

ABSTRACT

BACKGROUND: Residual atherosclerotic cardiovascular disease (ASCVD) risk remains common among adults treated with moderate-intensity statins, necessitating nonstatin therapy. Ezetimibe is the preferred first-line oral nonstatin therapy. However, bempedoic acid is emerging as an alternative, particularly in patients with statin intolerance. Cardiovascular outcomes with bempedoic acid among patients receiving moderate-intensity statins in routine care are not well-established.

OBJECTIVE: To compare cardiovascular outcomes associated with bempedoic acid vs ezetimibe when added to background moderate-intensity statin therapy in the real world.

METHODS: This retrospective cohort study used the TriNetX global federated health research network. Adults aged 18 years or older receiving moderate-intensity statin therapy with add-on bempedoic acid or ezetimibe were included. The primary outcome was a composite of stroke, myocardial infarction, ischemic heart disease, new-onset heart failure, or peripheral artery disease. Risk ratios (RRs) with 95% CIs were calculated.

RESULTS: After matching, 6706 patients were included (n = 3353 per cohort). Bempedoic acid was associated with a significantly lower risk of the composite outcome compared with ezetimibe (16.7% vs 22.8%; RR: 0.73; 95% CI: 0.63-0.84). All individual cardiovascular endpoints favored bempedoic acid. Low-density lipoprotein cholesterol (LDL-C) reduction was greater with ezetimibe.

CONCLUSION: Among adults on moderate-intensity statins, bempedoic acid was associated with significantly lower cardiovascular event rates compared with ezetimibe, despite smaller LDL-C reductions. These findings complement Cholesterol Lowering via Bempedoic Acid, an ACL-Inhibiting Regimen (CLEAR) Outcomes and suggest greater ASCVD risk-reducing potential for bempedoic acid than currently reflected in clinical guidelines.

PMID:41820083 | DOI:10.1016/j.jacl.2026.02.014