z-logo
Premium
Reclassification of prostate cancer risk using sequentially identified SNPs: Results from the REDUCE trial
Author(s) -
Chen Haitao,
Na Rong,
Packiam Vignesh T.,
Conran Carly A.,
Jiang Deke,
Tao Sha,
Yu Hongjie,
Lin Xiaoling,
Meng Wei,
Zheng S. Lilly,
Brendler Charles B.,
Helfand Brian T.,
Xu Jianfeng
Publication year - 2017
Publication title -
the prostate
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.295
H-Index - 123
eISSN - 1097-0045
pISSN - 0270-4137
DOI - 10.1002/pros.23369
Subject(s) - single nucleotide polymorphism , prostate cancer , medicine , oncology , cancer , biology , genetics , genotype , gene
Background Although the clinical validity of risk‐associated single nucleotide polymorphisms (SNPs) for assessment of disease susceptibility has been consistently established, risk reclassification from increasing numbers of implicated risk‐associated SNPs raises concern that it is premature for clinical use. Our objective is to assess the degree and impact of risk reclassification with the increasing number of SNPs. Methods A total of 3239 patients from the Reduction by Dutasteride of Prostate Cancer Events (REDUCE) trial were included. Four genetic risk scores (GRSs) were calculated based on sets of sequentially discovered prostate cancer (PCa) risk‐associated SNPs (17, 34, 51, and 68 SNPs). Results Pair‐wise correlation coefficients between sets of GRSs increased as more SNPs were included in the GRS: 0.80, 0.86, and 0.95 for 17 versus 34 SNPs, 34 versus 51 SNPs, and 51 versus 68 SNPs, respectively. Using a GRS of 1.5 as a cutoff for higher versus lower risk, reclassification rates of PCa risk decreased: 14.11%, 12.04%, and 8.15% for 17 versus 34 SNPs, 34 versus 51 SNPs, and 51 versus 68 SNPs, respectively. Evolving GRSs, nevertheless, provide a tool for further refining risk assessment. When all four sequential GRSs were considered, the detection rates of PCa for men whose GRSs were consistently <1.5, reclassified, and consistently ≥1.5 were 20.8%, 29.67%, and 39.26%, respectively ( P trend  = 1.12 × 10 −8 ). In comparison, the detection rates of PCa in men with negative or positive family history were 23.75% and 31.78%, respectively. Conclusions Risk assessment using currently available SNPs is justified. Multiple GRS values from evolving sets of SNPs provide a valuable tool for better refining risk.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here