# Preventing Atherosclerotic Cardiovascular Disease in Young Male Androgen Abusers

**Authors:** Peter Bond, Diederik L. Smit, Tijs Verdegaal, Willem de Ronde

PMC · DOI: 10.1002/clc.70257 · Clinical Cardiology · 2026-02-19

## TL;DR

Young men who abuse androgens face increased risk of heart disease due to effects on cholesterol, blood pressure, and blood vessels.

## Contribution

Highlights androgen abuse as an underrecognized risk enhancer for heart disease in young men and suggests tailored risk assessment methods.

## Key findings

- Androgen abuse negatively impacts lipid profiles, blood pressure, and vascular function.
- Conventional risk models may underestimate cardiovascular risk in androgen abusers.
- Subclinical atherosclerosis is associated with androgen abuse despite otherwise healthy profiles.

## Abstract

Androgen abuse among young men is a prevalent yet under recognized risk factor for atherosclerotic cardiovascular disease (ASCVD). Supraphysiological androgen exposure adversely affects lipoprotein profiles, blood pressure, and vascular function, potentially accelerating atherosclerosis even in otherwise healthy individuals. Conventional cardiovascular risk prediction models may underestimate risk in this population due to fluctuating biomarker profiles and other unaccounted risk‐increasing factors that are not captured in these models.

To review the mechanisms by which androgen abuse contributes to ASCVD, to highlight limitations of traditional risk stratification tools in this population, and to propose tailored approaches to risk assessment and prevention.

Narrative review of epidemiological, imaging, and mechanistic studies examining cardiovascular risk factors and subclinical atherosclerosis in androgen abusers.

Available evidence indicates that androgen abuse adversely affects lipid profiles, blood pressure, and vascular endothelial function, and is associated with increased subclinical atherosclerosis. Conventional risk prediction models may underestimate risk in this population due to young age, fluctuating biomarker profiles, and cumulative exposure effects not captured by standard algorithms.

Androgen abuse should be recognized as a cardiovascular risk‐enhancing factor in young men. Individualized risk assessment beyond traditional calculators may be warranted to guide preventive strategies in selected patients.

Androgen abuse is an underrecognized ASCVD risk enhancer in young men. Improved risk assessment—integrating androgen exposure, imaging, and individualized prevention—may help in the management of long‐term cardiovascular risk in this population.

## Linked entities

- **Chemicals:** androgen (PubChem CID 5995)
- **Diseases:** atherosclerotic cardiovascular disease (MONDO:1060134)

## Full-text entities

- **Genes:** CIMT (Carotid intimal medial thickness) [NCBI Gene 404677], AGT (angiotensinogen) [NCBI Gene 183] {aka ANHU, SERPINA8, hFLT1}, LPA (lipoprotein(a)) [NCBI Gene 4018] {aka AK38, APOA, LP}, APOB (apolipoprotein B) [NCBI Gene 338] {aka FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48}, PCSK9 (proprotein convertase subtilisin/kexin type 9) [NCBI Gene 255738] {aka FH3, FHCL3, HCHOLA3, LDLCQ1, NARC-1, NARC1}, LIPC (lipase C, hepatic type) [NCBI Gene 3990] {aka HDLCQ12, HL, HTGL}, EDN1 (endothelin 1) [NCBI Gene 1906] {aka ARCND3, ET1, HDLCQ7, PPET1, QME}
- **Diseases:** morbidity (OMIM:614963), endothelial dysfunction (MESH:D014652), calcification (MESH:D002114), ischemic stroke (MESH:D002544), acute myocardial infarction (MESH:D009203), cardiovascular disease (MESH:D002318), HL-deficient (OMIM:614025), male androgen abuser (MESH:D013734), familial hypercholesterolemia (MESH:D006938), muscle-related (MESH:D009133), ASCVD (MESH:D050197), hypertension (MESH:D006973), dyslipidemia (MESH:D050171), atherosclerotic plaque (MESH:D058226), Androgen abuse (MESH:D014770), obesity (MESH:D009765), CAC (MESH:D003324)
- **Chemicals:** bempedoic acid (MESH:C581236), 20-HETE (MESH:C055987), nandrolone decanoate (MESH:D000077603), testosterone enanthate (MESH:C004648), 17alpha-alkylated androgens (-), eicosanoid (MESH:D015777), mevalonate (MESH:D008798), sugar (MESH:D000073893), ezetimibe (MESH:D000069438), fiber (MESH:D004043), simvastatin (MESH:D019821), amphetamines (MESH:D000662), alcohol (MESH:D000438), norepinephrine (MESH:D009638), calcium (MESH:D002118), thiazide (MESH:D049971), cholesterol (MESH:D002784), rosuvastatin (MESH:D000068718), stanozolol (MESH:D013197), thromboxane A2 (MESH:D013928), testosterone (MESH:D013739), lipid (MESH:D008055), arachidonic acid (MESH:D016718)
- **Species:** Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097]

## Full text

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## Figures

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## References

78 references — full list in the complete paper: https://tomesphere.com/paper/PMC12917856/full.md

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Source: https://tomesphere.com/paper/PMC12917856