Jul 2026· Journal of Medical Genetics· pp. jmg-2026-111746· 0 citations· 39 references
Medicine
TL;DR
An integrated continuum genetic risk model, GenProb-PCa, improves PCa risk stratification beyond binary approaches by capturing heterogeneity in inherited risk and may enable more precise risk-based screening strategies.
Abstract
Background
Current clinical approaches to inherited prostate cancer (PCa) risk rely on binary classification of pathogenic variant (PV) carrier status without accounting for gene-specific heterogeneity or polygenic risk. We developed an integrated genetic risk model reflecting a continuum of inherited susceptibility.
Methods
In the UK Biobank (UKB; n=218 484), we evaluated associations of PVs in 11 clinically recommended genes and a polygenic risk score (PRS) with incident PCa using Cox models. A continuum model (GenProb-PCa) incorporating gene-specific PVs and PRS was developed and compared with binary PV-based models. Model performance was assessed using discrimination, calibration and continuous net reclassification index (cNRI). External validation was performed in a health system cohort, the Genomic Health Initiative (GHI; n=6590).
Results
Five genes (ATM, BRCA2, CHEK2, HOXB13, MSH2) and the PRS were independently associated with PCa risk (all p<0.001) in UKB. Compared with binary models, GenProb-PCa demonstrated superior discrimination (C-index 0.69 vs 0.52; p<0.001), with significant improvement in reclassification (cNRI 0.58; p<0.001). Findings were validated in GHI using the UKB-derived coefficients (C-index 0.64 vs 0.54, p<0.001; cNRI 0.31, p<0.001). Compared with binary PV-based models, 20% of non-PV carriers were reclassified to higher risk groups and 60% of carriers to lower risk groups. The model identified individuals at markedly elevated lifetime risk, with cumulative incidence exceeding 20% by age 75 among the top 8% of the distribution.
Conclusions
An integrated continuum genetic risk model, GenProb-PCa, improves PCa risk stratification beyond binary approaches by capturing heterogeneity in inherited risk. This framework may enable more precise risk-based screening strategies.
Germline PVs in NCCN-recommended DDR genes and the KLK3 I179T variant identify a subset of men at elevated risk of PCSM, including those with apparently localized disease.
Lucy Lu, Julian Xu, Zhu-Qing Shi et al.· Prostate Cancer and Prostati...· 1 citation
GenProb-PCSM transforms complex germline findings into a single inherited risk score for PCSM and metastatic progression and may facilitate clinical implementation of germline prognostic assessment in PCa.
Jun Wei, Zhu-Qing Shi, Lucy Lu et al.· The Prostate· 0 citations
BCa and inherited genetic susceptibility jointly contribute to increased risk of multiple common diseases, supporting the integration of genetic risk stratification into survivorship care.
Annabelle Ashworth, Zhu-Qing Shi, Huy Tran et al.· JNCI Cancer Spectrum· 0 citations
Background It remains unclear whether cardiovascular-kidney-metabolic (CKM) syndrome and genetic susceptibility are associated with cancer incidence. This study aims to evaluate the associations between CKM health status, genetic susceptibility, and cancer incidence, and to develop a machine learning-based prediction m...
Xue He, J. An, Chun-Jia Yan et al.· Frontiers in Endocrinology· 0 citations
Existing BC risk prediction models provided similar risk discrimination across multiple cohorts, although there was overestimation of risk for high-risk individuals, which supports development of a unified risk model for diverse populations that leverages appropriate incidence rates.
K. Brantley, T. Ahearn, E. Norton et al.· medRxiv· 0 citations
This first large-scale SNP-association study in Kazakh men shows allele-frequency profiles resembling East Asian rather than European populations, confirming the need for population-specific genetic risk-assessment tools.
K. Kazbekov, Yerbol Zhapparov, N. Shanazarov et al.· Genes· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.