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

  • The NBCS Collaborators
  • , The BCAC Consortium
  • , CTS Consortium
  • , The ABCTB Investigators
  • , Hagai Levi
  • , Shai Carmi
  • , Saharon Rosset
  • , Rinat Yerushalmi
  • , Aviad Zick
  • , Tamar Yablonski-Peretz
  • , Qin Wang
  • , Manjeet K. Bolla
  • , Joe Dennis
  • , Kyriaki Michailidou
  • , Michael Lush
  • , Thomas Ahearn
  • , Irene L. Andrulis
  • , Hoda Anton-Culver
  • , Antonis C. Antoniou
  • , Volker Arndt
  • Annelie Augustinsson, Päivi Auvinen, Laura Beane Freeman, Matthias Beckmann, Sabine Behrens, Marina Bermisheva, Clara Bodelon, Natalia V. Bogdanova, Stig E. Bojesen, Hermann Brenner, Helen Byers, Nicola Camp, Jose Castelao, Jenny Chang-Claude, María Dolores Chirlaque, Wendy Chung, Christine Clarke, Margriet J. Collee, Sarah Colonna, Fergus Couch, Angela Cox, Simon S. Cross, Kamila Czene, Mary Daly, Peter Devilee, Thilo Dork, Laure Dossus, Diana M. Eccles, A. Heather Eliassen, Mikael Eriksson, Gareth Evans, Peter Fasching, Olivia Fletcher, Antoinette Hollestelle
  • The Norwegian Radium Hospital
  • Vestre Viken Hospital
  • Section for Breast and Endocrine Surgery
  • Oslo University Hospital-Ullevål
  • Oslo University Hospital
  • Akershus University Hospital
  • Breast Cancer Research Consortium
  • Australian Breast Cancer Tissue Bank
  • The University of Sydney
  • Tel Aviv University
  • Hebrew University of Jerusalem
  • Rabin Medical Center Israel
  • Hadassah University Medical Centre
  • University of Cambridge
  • Cyprus Institute of Neurology and Genetics
  • National Cancer Institute (Bethesda, Md)
  • Lunenfeld-Tanenbaum Research Institute of Mount Sinai Hospital
  • University of Toronto
  • University of California at Irvine
  • German Cancer Research Center
  • Lund University
  • University of Eastern Finland
  • Kuopio University Hospital
  • University Hospital Erlangen
  • Institute of Biochemistry and Genetics, Ufa Scientific Center RAS
  • American Cancer Society
  • Hannover Medical School
  • N.N. Alexandrov Research Institute of Oncology and Medical Radiology
  • Copenhagen University Hospital (Nordvest)
  • University of Copenhagen
  • Manchester University NHS Foundation Trust
  • University of Utah School of Medicine
  • Xerencia de Xestion Integrada de Vigo-SERGAS
  • University Medical Center Hamburg-Eppendorf
  • Centro de Investigación Biomédica en Red (CIBER)
  • Columbia University
  • Mayo Clinic Rochester, MN
  • University of Sheffield
  • Karolinska Institutet
  • Fox Chase Cancer Center
  • Leiden University Medical Centre
  • Leiden University
  • International Agency for Research on Cancer
  • University of Southampton
  • Harvard University
  • Harvard T.H. Chan School of Public Health
  • University of Manchester
  • Institute of Cancer Research (ICR), London

Research output: Contribution to journalArticleAcademicpeer-review

5 Citations (Scopus)
116 Downloads (Pure)

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
Article numberjmg-2023-109185
Pages (from-to)1186-1197
Number of pages12
JournalJournal of medical genetics
Volume60
Issue number12
Early online date14 Jul 2023
DOIs
Publication statusPublished - 1 Dec 2023

Bibliographical note

Publisher Copyright:
© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY. Published by BMJ.

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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