# Blood inflammatory markers combined with tumor markers for differentiating benign prostatic hyperplasia from prostate cancer

**Authors:** Zeqiang Liu, Xinji Yang, Xiaofei Hou, Peng Du, Keke Jia

PMC · DOI: 10.3389/fmed.2026.1730818 · Frontiers in Medicine · 2026-02-04

## TL;DR

This study shows that blood inflammatory markers, especially AISI, can help distinguish prostate cancer from benign prostatic hyperplasia more accurately than current methods.

## Contribution

The study introduces a novel combination of blood inflammatory markers and tumor markers for improved PCa diagnosis.

## Key findings

- PCa patients had significantly higher inflammatory marker levels than BPH patients.
- AISI-based models outperformed SII-based models with an AUC of 0.878.
- AISI in combination with conventional biomarkers offers enhanced diagnostic accuracy.

## Abstract

Prostate cancer (PCa) is the second most frequently diagnosed malignancy in men worldwide, whereas benign prostatic hyperplasia (BPH) is among the most prevalent non-malignant prostatic disorders. Differentiating between these two conditions remains challenging because of overlapping clinical manifestations and the limited specificity of currently available biomarkers.

This retrospective study enrolled 200 male patients (53 PCa, 147 BPH) who underwent prostate biopsy or surgical resection based on pathological diagnosis. Clinical characteristics, laboratory parameters, and inflammatory indices were compared between the groups. Both univariate and multivariate logistic regression analyses were conducted to identify independent predictors. Nomograms were developed and validated through calibration curves, ROC analysis, and decision curve analysis (DCA).

PCa patients had significantly higher levels of inflammatory markers than BPH patients (p < 0.05). In multivariate analysis, log2-SII (OR = 2.22, 95% CI: 1.13–4.37, p = 0.021) and log2-AISI (OR = 3.27, 95% CI: 1.83–5.85, p < 0.001) emerged as independent risk factors for PCa. The AISI-based model achieved superior diagnostic performance with an AUC of 0.878 (95% CI: 0.825–0.931) compared with the SII-based model (AUC = 0.855, 95% CI: 0.794–0.915). DCA showed greater clinical net benefit for the AISI model across a wide range of threshold probabilities.

Blood inflammatory markers, particularly AISI, in combination with conventional biomarkers, offer enhanced diagnostic accuracy for differentiating BPH from PCa, representing a non-invasive and cost-effective approach for clinical decision-making.

## Linked entities

- **Diseases:** prostate cancer (MONDO:0005159), benign prostatic hyperplasia (MONDO:0010811)

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, CST3 (cystatin C) [NCBI Gene 1471] {aka ADLDWA, ARMD11, HEL-S-2}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}, F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, MUC1 (mucin 1, cell surface associated) [NCBI Gene 4582] {aka ADMCKD, ADMCKD1, ADTKD2, CA 15-3, CD227, Ca15-3}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, MUC16 (mucin 16, cell surface associated) [NCBI Gene 94025] {aka CA125}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, MPO (myeloperoxidase) [NCBI Gene 4353], TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}
- **Diseases:** renal function (MESH:D058186), carcinogenesis (MESH:D063646), bleeding (MESH:D006470), non-small cell lung cancer (MESH:D002289), urinary dysfunction (MESH:D001745), coronary heart disease (MESH:D003327), nodules (MESH:D016606), pain (MESH:D010146), PCa (MESH:D011471), BOO (MESH:D001748), AISI (MESH:D007249), malignant epithelial tumors (MESH:D002277), diabetes (MESH:D003920), Tumor (MESH:D009369), adenocarcinoma (MESH:D000230), psychiatric disorders (MESH:D001523), lung cancer (MESH:D008175), coronary artery disease (MESH:D003324), Prostate acinar adenocarcinoma (MESH:D018267), solid (MESH:D018250), prostate malignancy (MESH:D011472), hepatocellular carcinoma (MESH:D006528), hematological disorders (MESH:D006402), hypertension (MESH:D006973), carcinogenic (MESH:D011230), deaths (MESH:D003643), urological malignancies (MESH:D014571), Abnormal hepatic or renal function (MESH:D000014), metastasis (MESH:D009362), prostatic diseases (MESH:D011469), BPH (MESH:D011470), immune system diseases (MESH:D007154), LUTS (MESH:D059411), cardiovascular diseases (MESH:D002318), infection (MESH:D007239)
- **Chemicals:** CHO (MESH:C034482), cholesterol (MESH:D002784), Glu (MESH:D018698), T (MESH:D014316), triglycerides (MESH:D014280), bilirubin (MESH:D001663), lipid (MESH:D008055), steroid hormone (MESH:D013256), reactive oxygen species (MESH:D017382), glucose (MESH:D005947), Alcohol (MESH:D000438), acetaldehyde (MESH:D000079), TG (MESH:D013866), CysC (-)
- **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/PMC12913570/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12913570/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913570/full.md

---
Source: https://tomesphere.com/paper/PMC12913570