# Elevated low-density lipoprotein cholesterol levels and prostate cancer risk: UK Biobank evidence

**Authors:** R. Alexa, J. Kranz, M. Thöne, S. Grundl, M. Hoffmann, P. H. Koop, C. Feng, K. M. Schneider, C. Schneider, M. Saar

PMC · DOI: 10.1007/s00345-026-06313-4 · World Journal of Urology · 2026-02-27

## TL;DR

Higher LDL cholesterol levels are linked to a lower risk of prostate cancer in a large UK study, independent of heart disease factors.

## Contribution

This study provides new evidence that elevated LDL cholesterol is inversely associated with prostate cancer risk in a large cohort.

## Key findings

- Elevated LDL cholesterol (≥3.65 mmol/L) was associated with a reduced risk of prostate cancer (HR = 0.83).
- The association remained significant after adjusting for cardiovascular morbidity and mortality.
- Elevated ALT and diabetes mellitus were also found to have protective associations with prostate cancer risk.

## Abstract

Hepatic lipid metabolism has been implicated in cancer development, with cholesterol dysregulation linked to tumor initiation and progression. We examined the association between low-density lipoprotein cholesterol (LDL) levels and prostate cancer (PCa) risk in the UK Biobank cohort.

This multicenter, community-based cohort study, conducted from March 2006 to December 2010, included 502,511 participants from the UK Biobank. Morbidity and mortality were analyzed in August 2023. Hazard ratios (HRs) for PCa related to hepatic blood value changes were calculated, adjusting for key variables.

We extracted 204,403 healthy men and 13,205 PCa patients, subdivided into 3751 with PCa at inclusion and 9454 who developed PCa during 14.1 years of follow-up. Elevated LDL ≥ 3.65 mmol/L was associated with a reduced risk of PCa (HR = 0.83, 95% CI = 0.77–0.90, p < 0.01). To exclude confounding from cardiovascular morbidity, we compared the prevalence of myocardial infarction, stroke, and peripheral arterial disease between LDL groups. The combined prevalence of myocardial infarction, stroke, or peripheral arterial disease was similar between low and high LDL (2.67% vs. 2.49%; OR = 0.93, p < 0.01). Fine–Gray competing risk models further confirmed that high LDL remained inversely associated with PCa risk (sHR = 0.92, 95% CI = 0.88–0.96, p < 0.01), indicating that the observed association is not explained by excess cardiovascular mortality or differential cardiovascular morbidity. A significant association was also found between paternal PCa and the risk of PCa (HR = 1.34, 95% CI = 1.16–1.54, p < 0.01). Elevated alanine aminotransferase (ALT ≥ 50 U/L) was protective (HR = 0.69, 95% CI = 0.56–0.84, p < 0.01), and matched cohort analyses confirmed a protective association with diabetes mellitus (HR = 0.78, 95% CI = 0.68–0.90, p < 0.01).

Elevated LDL was consistently associated with a reduced risk of PCa, independent of cardiovascular morbidity and competing mortality. ALT elevation and diabetes mellitus also showed protective associations, though less pronounced.

The online version contains supplementary material available at 10.1007/s00345-026-06313-4.

## Linked entities

- **Diseases:** prostate cancer (MONDO:0005159), myocardial infarction (MONDO:0005068), stroke (MONDO:0005098), peripheral arterial disease (MONDO:0005386), diabetes mellitus (MONDO:0005015)

## Full-text entities

- **Genes:** IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370] {aka ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1}, ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}
- **Diseases:** cancer (MESH:D009369), Diabetes mellitus (MESH:D003920), dyslipidemia (MESH:D050171), metabolic disturbances (MESH:D024821), PCa (MESH:D011471), inflammatory (MESH:D007249), frailty (MESH:D000073496), stroke (MESH:D020521), Obesity (MESH:D009765), Cardiovascular comorbidities (MESH:D002318), MI (MESH:D009203), PCA (MESH:C562643), death (MESH:D003643), liver metastasis (MESH:D009362), long-term diabetes (MESH:D000088562), breast cancer (MESH:D001943), hypercholesterolemia (MESH:D006937), type 2 diabetes (MESH:D003924), peripheral arterial disease (MESH:D058729)
- **Chemicals:** alanine (MESH:D000409), Cholesterol (MESH:D002784), LDL cholesterol (-), glucose (MESH:D005947), lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12948794/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12948794/full.md

## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC12948794/full.md

---
Source: https://tomesphere.com/paper/PMC12948794