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Genetic risk and likelihood of prostate cancer detection on first biopsy by ancestry. | LitMetric

AI Article Synopsis

  • - This study analyzed the effectiveness of a genetic risk score (PHS290) in predicting prostate cancer diagnoses during initial biopsies among 36,717 male veterans, including 10,297 of African ancestry.
  • - Higher genetic risk correlated with increased rates of positive biopsies, with low-risk men having a 34% detection rate compared to 58% for high-risk men (P < .001).
  • - Although higher genetic risk significantly increased detection rates for both African and European ancestry groups, it was notably stronger for European men (odds ratio of 3.89 vs. 2.18 for African ancestry), indicating a need for more equitable genetic risk assessments across different ancestry groups.

Article Abstract

Despite differences in prostate cancer risk across ancestry groups, relative performance of prostate cancer genetic risks scores (GRS) for positive biopsy prediction in different ancestry groups is unknown. This cross-sectional retrospective analysis examines the association between a polygenic hazard score (PHS290) and risk of prostate cancer diagnosis upon first biopsy in male veterans using 2-sided tests. Our analysis included 36 717 veterans (10 297 of African ancestry). Unadjusted rates of positive first prostate biopsy increased with higher genetic risk (low risk: 34%, high risk: 58%; P < .001). Among men of African ancestry, higher genetic risk was associated with increased prostate cancer detection on first biopsy (odds ratio = 2.18, 95% confidence interval = 1.93 to 2.47), but the effect was stronger among men of European descent (odds ratio = 3.89, 95% confidence interval = 3.62 to 4.18). These findings suggest that incorporating genetic risk into prediction models could better personalize biopsy decisions, although further study is needed to achieve equitable genetic risk stratification among ancestry groups.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11077300PMC
http://dx.doi.org/10.1093/jnci/djae002DOI Listing

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