# Ezetimibe alone for over 75 years old as a primary prevention to decrease cardiovascular events

**Authors:** Alpo Vuorio, Petri T. Kovanen, Timo Strandberg

PMC · DOI: 10.1080/07853890.2026.2634484 · Annals of Medicine · 2026-02-24

## TL;DR

Ezetimibe alone can reduce cardiovascular risk in older adults without prior heart disease, possibly due to its effect on cholesterol absorption.

## Contribution

The study provides evidence that ezetimibe monotherapy is effective in reducing ASCVD events in elderly individuals without statin use.

## Key findings

- Ezetimibe reduces cardiovascular events in older adults without coronary artery disease.
- Cholesterol absorption efficiency increases with age, making ezetimibe particularly beneficial in the elderly.

## Abstract

The EWTOPIA 75 (Ezetimibe Lipid-Lowering Trial on Prevention of Atherosclerotic Cardiovascular Disease in 75 or Older) study supports the reduction in the risk of atherosclerotic cardiovascular disease (ASCVD) events with ezetimibe without statin therapy in persons aged ≥75 years without a history of coronary artery disease. This evidence has also been incorporated into the 2025 Focused Update of the 2019 ESC/EAS Guidelines for the management of dyslipidaemias. What might then be the potential explanations for the observed benefit of ezetimibe to prevent ASCVD in the EWTOPIA 75 study? First, cholesterol absorption efficiency generally increases with age. Therefore, cholesterol absorption-lowering medications, such as ezetimibe, are particularly beneficial in individuals aged 75 years and older, in whom low cholesterol absorption has been associated with fewer recurrent ASCVD events. It is also worth noting that ezetimibe may be more effective than a particular statin in reducing non-high-density lipoprotein cholesterol (non-HDL-C), which includes lipoprotein remnant particles. Therefore, the benefits of the achieved low-density lipoprotein cholesterol (LDL-C) levels are not directly comparable between ezetimibe and statin therapy. It remains to be verified in future studies whether ezetimibe monotherapy would be helpful, specifically in older patients. If so, one possible explanation is that, even in the absence of clinical ASCVD, ezetimibe slows and stabilizes the atherosclerotic process that is still advancing. Finally, a trade-off between a less effective LDL-C lowering but a low frequency of adverse effects and drug interactions could lead to better long-term adherence in the setting of primary prevention.

Cholesterol absorption efficiency generally increases with age.

Ezetimibe alone reduces the risk of cardiovascular events in persons aged ≥75 years without a history of coronary artery disease.

## Linked entities

- **Chemicals:** ezetimibe (PubChem CID 150311)
- **Diseases:** atherosclerotic cardiovascular disease (MONDO:1060134), coronary artery disease (MONDO:0005010)

## Full-text entities

- **Genes:** APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}, NPC1L1 (NPC1 like intracellular cholesterol transporter 1) [NCBI Gene 29881] {aka LDLCQ7, NPC11L1, SLC65A2}
- **Diseases:** stroke (MESH:D020521), metabolic disease (MESH:D008659), frailty (MESH:D000073496), hepatic impairment (MESH:D008107), inflammation (MESH:D007249), diabetes (MESH:D003920), endothelial dysfunction (MESH:D014652), renal insufficiency (MESH:D051437), hypercholesterolemia (MESH:D006937), coronary artery disease (MESH:D003324), atherosclerotic plaques (MESH:D058226), ASCVD (MESH:D050197), cardiac death (MESH:D003643), Cardiovascular Disorders (MESH:D002318), myocardial infarction (MESH:D009203)
- **Chemicals:** Cholesterol (MESH:D002784), campesterol (MESH:C021273), Ezetimibe (MESH:D000069438), phytosterol (MESH:D010840), Lipid (MESH:D008055), lathosterol (MESH:C001521), Ezetimibe Phytosterol (-), atorvastatin (MESH:D000069059), cholestanol (MESH:D004083), Pravastatin (MESH:D017035)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12934334/full.md

## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC12934334/full.md

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Source: https://tomesphere.com/paper/PMC12934334