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African-specific improvement of a polygenic hazard score for age at diagnosis of prostate cancer

  • UKGPCS Collaborators
  • , The PRACTICAL Consortium
  • The Institute of Cancer Research
  • University of California at San Diego
  • Healthlytix
  • Royal Marsden NHS Foundation Trust
  • University of Manchester
  • University of Warwick
  • Fred Hutchinson Cancer Research Center
  • CHRISTUS Santa Rosa Hospital
  • Vanderbilt University
  • International Epidemiology Institute
  • Brigham and Women’s Hospital
  • Washington University St. Louis
  • Sorbonne Université
  • Tenon Hospital
  • Université Paris-Saclay
  • Moffitt Cancer Center
  • Louisiana State University Health Sciences Center
  • University of North Carolina at Chapel Hill
  • University of North Carolina at Chapel Hill
  • National Institutes of Health
  • School of Public Health
  • Université des Antilles
  • Université Paris Sorbonne Cité
  • University of Texas Health Science Center at San Antonio
  • Stanford University
  • University of Tennessee Health Science Center
  • Case Western Reserve University
  • Uniformed Services University of the Health Sciences
  • Center for Prostate Disease Research
  • Institut national de la recherche scientifique
  • University of Montreal
  • University of Miami
  • Meharry Medical College
  • Queen's University Belfast
  • University of Oslo

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

Polygenic hazard score (PHS) models are associated with age at diagnosis of prostate cancer. Our model developed in Europeans (PHS46) showed reduced performance in men with African genetic ancestry. We used a cross-validated search to identify single nucleotide polymorphisms (SNPs) that might improve performance in this population. Anonymized genotypic data were obtained from the PRACTICAL consortium for 6253 men with African genetic ancestry. Ten iterations of a 10-fold cross-validation search were conducted to select SNPs that would be included in the final PHS46+African model. The coefficients of PHS46+African were estimated in a Cox proportional hazards framework using age at diagnosis as the dependent variable and PHS46, and selected SNPs as predictors. The performance of PHS46 and PHS46+African was compared using the same cross-validated approach. Three SNPs (rs76229939, rs74421890 and rs5013678) were selected for inclusion in PHS46+African. All three SNPs are located on chromosome 8q24. PHS46+African showed substantial improvements in all performance metrics measured, including a 75% increase in the relative hazard of those in the upper 20% compared to the bottom 20% (2.47-4.34) and a 20% reduction in the relative hazard of those in the bottom 20% compared to the middle 40% (0.65-0.53). In conclusion, we identified three SNPs that substantially improved the association of PHS46 with age at diagnosis of prostate cancer in men with African genetic ancestry to levels comparable to Europeans.

Original languageEnglish
Pages (from-to)99-105
Number of pages7
JournalInternational Journal of Cancer
Volume148
Issue number1
DOIs
StatePublished - Jan 1 2021

Keywords

  • African
  • genome wide association study
  • genomics
  • genotypic ancestry
  • health disparities
  • polygenic risk
  • prostate cancer

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