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Genetically adjusted prostate-specific antigen values may prevent delayed biopsies in African-American men
Nicholas M Donin1, Stacy Loeb1, Phillip R Cooper2
1Department of Urology, New York University Langone Medical Center and Manhattan Veterans Affairs Medical Center, New York, NY, USA.
BJU International
|April 10, 2014
Summary
Genetic correction using prostate-specific antigen (PSA)-single nucleotide polymorphisms (SNPs) did not reduce unnecessary biopsies in African-American men. However, it significantly reduced potentially delayed prostate cancer biopsies by 2.5-3.9%.
Area of Science:
- Genetics
- Urology
- Oncology
Background:
- Prostate cancer (PCa) disproportionately affects African-American men.
- Genetic variants in prostate-specific antigen (PSA)-single nucleotide polymorphisms (SNPs) may influence PSA levels.
- Current biopsy guidelines may not account for genetic variations.
Purpose of the Study:
- To evaluate if genetic correction of PSA-SNP variants could decrease unnecessary or delayed prostate cancer biopsies in African-American men.
- To compare the impact of PSA-SNP genotypes between African-American and Caucasian men.
Main Methods:
- Compared genotypes of four PSA-SNPs in 964 Caucasian and 363 African-American men without known PCa.
- Adjusted PSA values based on individual PSA-SNP carrier status.
- Calculated biopsy threshold adherence before and after genetic correction.
Main Results:
- Genetic correction did not avoid any potentially unnecessary biopsies in African-American men.
- A significant reduction (P < 0.001) in potentially delayed biopsies was observed: 2.5% for PSA ≥ 2.5 ng/mL and 3.9% for PSA ≥ 4.0 ng/mL.
- Significant differences in PSA-SNP influence were noted between African-American and Caucasian men.
Conclusions:
- Genetic correction of PSA-SNPs increased the proportion of African-American men crossing the biopsy threshold.
- These findings suggest genetic differences in PSA may contribute to delayed prostate cancer diagnosis in African-American men.
- Further research is needed to understand the role of genetic variations in PCa diagnosis for this population.

