# Use of a BMI-independent biomarker-based prostate cancer risk score to identify and triage individuals at risk of prostate disease

**Authors:** Joanne Watt, Allister Irvine, Mary Jo Kurth, Laura Mooney, Gary Smyth, Hardev Pandha, John Lamont, Peter Fitzgerald, Le Roy Dowey, Mark W. Ruddock

PMC · DOI: 10.1038/s41598-025-13036-w · 2025-07-24

## TL;DR

A new BMI-independent prostate cancer risk score could improve cancer detection in overweight men where traditional tests are less reliable.

## Contribution

A novel biomarker-based risk score that is not affected by BMI was developed and shown to outperform tPSA in certain populations.

## Key findings

- 90.5% of the cohort had low prostate cancer risk based on the new PCRS.
- 67.8% of men with elevated PCRS had normal tPSA levels.
- BMI had a negative correlation with tPSA but not with PCRS.

## Abstract

Prostate cancer (PCa) is the second most common cause of cancer related deaths in men in the UK. A national screening programme for PCa does not exist due to the unsuitability of the total prostate specific antigen (tPSA) test which is not specific for PCa and has a high false positive rate. Serum tPSA was measured in n = 25,356 male Randox Health clients. A biomarker-based (tPSA, EGF, MCP-1, IL-8) prostate cancer risk score (PCRS) was then applied to a retrospective cohort (n = 1,142/25,356) of individuals to assess PCa risk. A comparative analysis between tPSA and PCRS indicated that 90.5% of the cohort were assigned low risk of PCa. Of those with an elevated PCRS, 67.8% (78/115) had a normal tPSA value based on tPSA age-adjusted cut-offs. In addition, we observed a significant negative correlation between increasing body mass index (BMI) in men with high BMI (≥ 30) and tPSA levels. No correlation was observed between BMI and PCRS. The tPSA test is potentially unsuitable for use in males with BMI ≥ 30. Use of PCRS could provide more accurate PCa risk stratification for males with BMI ≥ 30. Future assessment of the clinical utility of PCRS is warranted.

The online version contains supplementary material available at 10.1038/s41598-025-13036-w.

## Linked entities

- **Proteins:** tpsA (glycosyltransferase family 20 protein), EGF (epidermal growth factor), CCL2 (C-C motif chemokine ligand 2), CXCL8 (C-X-C motif chemokine ligand 8)
- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}
- **Diseases:** prostate disease (MESH:D011469), cancer (MESH:D009369), PCa (MESH:D011471)
- **Chemicals:** tPSA (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12287467/full.md

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Source: https://tomesphere.com/paper/PMC12287467