# Implementation of risk-based lipid-lowering therapies in older (age ≥ 65 years) and very-old adults (age ≥ 75 years) with ischemic heart disease in the greater Salzburg region

**Authors:** Kristen Kopp, Lukas J. Motloch, Bernhard Wernly, Alexander E. Berezin, Victoria Maringgele, Anna Dieplinger, Uta C. Hoppe, Michael Lichtenauer

PMC · DOI: 10.3389/fphar.2024.1357334 · Frontiers in Pharmacology · 2024-06-19

## TL;DR

This study examines how well lipid-lowering therapies are used in older and very-old adults with heart disease in Salzburg, finding suboptimal treatment and LDL cholesterol target achievement.

## Contribution

The study provides new insights into the implementation of lipid-lowering therapies in older and very-old adults with ischemic heart disease in a specific regional population.

## Key findings

- Less than 40% of high-/very-high-risk patients had prior lipid-lowering therapy use, with no significant age differences.
- Only 22%–30% of older/very-old adults met stricter LDL-C targets (<55 mg/dL) despite being on low-/moderate-intensity statins.
- Oldest adults (≥75 years) met risk-based LDL-C targets more frequently than younger groups, despite limited use of advanced therapies.

## Abstract

Introduction: European guidelines recommend the implementation of lipid-lowering therapies (LLTs) in adults (≥ 65 years) with established atherosclerotic cardiovascular disease (ASCVD) and for risk-based primary prevention in older adults (≤ 75 years), yet their use in very-old adults (> 75 years) is controversial, discretionary, and oriented on the presence of risk factors. The aim of this retrospective study is to assess guideline-directed LLT implementation and low-density lipoprotein cholesterol (LDL-C) target achievement in high-/very-high-risk older/very-old adults (65–74 and ≥ 75 years) at presentation for ST-segment elevation myocardial infarction (STEMI) and also to assess evidence-based care delivery to older adults in our region.

Methods: All STEMI patients with available LDL-C and total cholesterol presenting for treatment at a large tertiary center in Salzburg, Austria, 2018–2020, were screened (n = 910). High-risk/very-high-risk patients (n = 369) were classified according to European guidelines criteria and divided into cohorts by age: < 65 years (n = 152), 65–74 years (n = 104), and ≥ 75 years (n = 113).

Results: Despite being at high-/very-high-risk, prior LLT use was < 40% in the total cohort, with no significant difference by age. Statin monotherapy predominated; 20%–23% of older/very-old adults in the entire cohort were using low-/moderate-intensity stains, 11%–13% were using high-intensity statins, 4% were on ezetimibe therapy, and none were taking proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors. In the secondary prevention cohort, 53% of older/very-old patients used prior LLTs. Significantly higher percentages of older/oldest ASCVD patients (43% and 49%) met LDL-C targets < 70 mg/dL compared to patients < 65 years (29%; p = 0.033), although just 22% and 30% of these older groups attained stricter LDL-C targets of < 55 mg/dL. Low LLT uptake (16%) among older adults aged 64–74 years for primary prevention resulted in 17% and 10% attainment of risk-based LDL-C targets < 70 mg/dL and < 55 mg/dL, respectively. Oldest adults (≥ 75 years) in both primary and secondary prevention groups more often met risk-based targets than older and younger adults, despite predominantly receiving low-/moderate-intensity statin monotherapy.

Conclusion: Secondary prevention was sub-optimal in our region. Less than half of older/very-old adults with established ASCVD met LDL-C targets at the time of STEMI, suggesting severe care-delivery deficits in LLT implementation. Shortcomings in initiation of risk-based LLTs were also observed among high-/very-high-risk primary prevention patients < 75 years, with the achievement of risk-based LDL-C targets in 10%–48% of these patients.

## Linked entities

- **Diseases:** atherosclerotic cardiovascular disease (MONDO:1060134), ST-segment elevation myocardial infarction (MONDO:0041656)

## Full-text entities

- **Genes:** PCSK9 (proprotein convertase subtilisin/kexin type 9) [NCBI Gene 255738] {aka FH3, FHCL3, HCHOLA3, LDLCQ1, NARC-1, NARC1}
- **Diseases:** myocardial infarction (MESH:D009203), STEMI (MESH:D000072657), ischemic heart disease (MESH:D017202), ASCVD (MESH:D050197)
- **Chemicals:** LLT (-), ezetimibe (MESH:D000069438), lipid (MESH:D008055), cholesterol (MESH:D002784)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC11223559/full.md

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Source: https://tomesphere.com/paper/PMC11223559