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Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel

  • The BCAC Consortium
  • , NBCS Collaborators
  • , CTS Consortium
  • , ABCTB Investigators
  • , Hagai Levi
  • , Shai Carmi
  • , Saharon Rosset
  • , Rinat Yerushalmi
  • , Aviad Zick
  • , Tamar Yablonski-Peretz
  • , Ron Shamir*
  • , Ran Elkon*
  • , Naama Elefant*
  • *Corresponding author for this work
  • Hebrew University of Jerusalem
  • Rabin Medical Center Israel
  • Hadassah University Medical Centre
  • University of Cambridge
  • Cyprus Institute of Neurology and Genetics
  • National Institutes of Health
  • University of Toronto
  • University of California at Irvine
  • German Cancer Research Center
  • Lund University
  • University of Eastern Finland
  • Friedrich-Alexander University Erlangen-Nürnberg
  • Russian Academy of Sciences
  • American Cancer Society
  • Hannover Medical School
  • Settlement of Lesnoy-2
  • University of Copenhagen
  • Manchester University NHS Foundation Trust
  • University of Utah
  • Instituto de Investigacion Sanitaria Galicia Sur (IISGS)
  • University of Hamburg
  • Centro de Investigación Biomédica en Red
  • Columbia University
  • The University of Sydney
  • Erasmus University Rotterdam
  • Mayo Clinic Rochester, MN
  • University of Sheffield
  • Karolinska Institutet
  • Fox Chase Cancer Center
  • Leiden University
  • International Agency for Research on Cancer
  • University of Southampton
  • Harvard University
  • University of Manchester
  • Australian Breast Cancer Tissue Bank
  • Institute of Cancer Research
  • Curtin University
  • Complejo Hospitalario Universitario de Santiago
  • Hospital Clínico San Carlos de Madrid
  • Herbert Irving Comprehensive Cancer Center
  • Cancer Council Victoria
  • University of Melbourne
  • Monash University
  • McGill University
  • CESP
  • Robert Bosch Foundation
  • University of Tübingen
  • Research Centre for Genetic Engineering and Biotechnology’Georgi D. Efremov’
  • Pomeranian Medical University in Szczecin
  • Stanford University
  • Memorial Sloan-Kettering Cancer Center
  • Ufa University of Science and Technology
  • University of Oslo
  • City of Hope National Med Center
  • KU Leuven
  • Flanders Institute for Biotechnology
  • University of Hawai'i at Mānoa
  • Clalit Health Services
  • GmbH
  • Heraklion University Hospital
  • University College London
  • University Health Network
  • University of British Columbia
  • Provincial Health Services Authority
  • University of North Carolina at Chapel Hill
  • University of Naples Federico II
  • FIRC Institute of Molecular Oncology
  • Ulm University
  • IRCCS Fondazione Istituto Nazionale per lo studio e la cura dei tumori - Milano
  • University Hospital of Larissa
  • Netherlands Cancer Institute
  • Antoni van Leeuwenhoek Hospital
  • University of Kansas
  • Université Laval
  • University of Western Australia
  • Ohio State University
  • Vanderbilt University
  • Cedars-Sinai Medical Center

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Background Polygenic risk score (PRS), calculated based on genome-wide association studies (GWASs), can improve breast cancer (BC) risk assessment. To date, most BC GWASs have been performed in individuals of European (EUR) ancestry, and the generalisation of EUR-based PRS to other populations is a major challenge. In this study, we examined the performance of EUR-based BC PRS models in Ashkenazi Jewish (AJ) women. Methods We generated PRSs based on data on EUR women from the Breast Cancer Association Consortium (BCAC). We tested the performance of the PRSs in a cohort of 2161 AJ women from Israel (1437 cases and 724 controls) from BCAC (BCAC cohort from Israel (BCAC-IL)). In addition, we tested the performance of these EUR-based BC PRSs, as well as the established 313-SNP EUR BC PRS, in an independent cohort of 181 AJ women from Hadassah Medical Center (HMC) in Israel. Results In the BCAC-IL cohort, the highest OR per 1 SD was 1.56 (±0.09). The OR for AJ women at the top 10% of the PRS distribution compared with the middle quintile was 2.10 (±0.24). In the HMC cohort, the OR per 1 SD of the EUR-based PRS that performed best in the BCAC-IL cohort was 1.58±0.27. The OR per 1 SD of the commonly used 313-SNP BC PRS was 1.64 (±0.28). Conclusions Extant EUR GWAS data can be used for generating PRSs that identify AJ women with markedly elevated risk of BC and therefore hold promise for improving BC risk assessment in AJ women.

Original languageEnglish
Pages (from-to)1186-1197
Number of pages12
JournalJournal of Medical Genetics
Volume60
Issue number12
DOIs
StatePublished - 1 Dec 2023

Funding

FundersFunder number
UK Research and Innovation
Horizon 2020 Framework Programme634935
European Commission294576
National Health and Medical Research Council400281, 400413, 199600
Medical Research CouncilMR/M012190/1
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Wellcome Trust203477, 104036, 207800

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

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