# Evaluation of bempedoic acid in elderly patients: real-world evidence from the REALIST study

**Authors:** Saverio Muscoli, Emanuele Di Marco, Fiorella Puttini, Sara Sposini Ghezzi, Mihaela Ifrim, Mobina Amtaeh, Emanuele Maria Renga, Caterina Cappello, Giulio Barone, Gaetano Chiricolo, Giuseppe Massimo Sangiorgi, Andrea Natale, David Della-Morte

PMC · DOI: 10.3389/fragi.2026.1675989 · Frontiers in Aging · 2026-03-11

## TL;DR

Bempedoic acid effectively lowers cholesterol in elderly patients without major side effects, offering a new option for those who can't take statins.

## Contribution

Demonstrates bempedoic acid's efficacy and safety in elderly patients with high cardiovascular risk.

## Key findings

- Bempedoic acid significantly reduced LDL-C, triglycerides, and total cholesterol in elderly patients.
- Renal and hepatic function remained stable, with only a slight increase in uric acid observed.
- No treatment discontinuations occurred, indicating good tolerability in this high-risk group.

## Abstract

Statin intolerance and PCSK9 inhibitor reimbursement restrictions limit lipid-lowering options for elderly patients at high cardiovascular (CV) risk. Bempedoic acid (BA), an ATP-citrate lyase inhibitor, is a promising alternative. This study analyzed 54 patients over 81 years, selected from 2,564 individuals with medium to very high CV risk, who received BA for 52 weeks. Lipid profiles, renal and hepatic function, and adverse events were assessed. BA significantly reduced Low-Density Lipoprotein Cholesterol (LDL-C), triglycerides, and total cholesterol while maintaining stable HDL-C levels. Renal and hepatic function remained unchanged, with increased uric acid as the only notable adverse event. No treatment discontinuations occurred. During follow-up, five patients underwent coronary angiography, two developed atrial fibrillation, and two were hospitalized for heart failure. BA demonstrated efficacy and tolerability in this high-risk, elderly population. It represents a viable lipid-lowering option for statin-intolerant patients or those ineligible for PCSK9 inhibitors. Further studies are needed to confirm long-term cardiovascular benefits.

## Linked entities

- **Chemicals:** bempedoic acid (PubChem CID 10472693), uric acid (PubChem CID 1175)
- **Diseases:** atrial fibrillation (MONDO:0004981), heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** PCSK9 (proprotein convertase subtilisin/kexin type 9) [NCBI Gene 255738] {aka FH3, FHCL3, HCHOLA3, LDLCQ1, NARC-1, NARC1}, ACLY (ATP citrate lyase) [NCBI Gene 47] {aka ACL, ATPCL, CLATP}
- **Diseases:** atrial fibrillation (MESH:D001281), heart failure (MESH:D006333)
- **Chemicals:** cholesterol (MESH:D002784), BA (MESH:C581236), Lipid (MESH:D008055), triglycerides (MESH:D014280), uric acid (MESH:D014527)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13013346/full.md

## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC13013346/full.md

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Source: https://tomesphere.com/paper/PMC13013346