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Article: Breast cancer polygenic risk scores derived in White European populations are not calibrated for women of Ashkenazi Jewish descent.

  • Eleanor Roberts
    Affiliations
    Division of Cancer Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK
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  • Elke M. van Veen
    Affiliations
    Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester, UK

    Division of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK
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  • Helen Byers
    Affiliations
    Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester, UK

    Division of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK
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  • Ofra Barnett-Griness
    Affiliations
    Department of Community Medicine and Epidemiology, Carmel Medical Center, Haifa 3436217, Israel
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  • Naomi Gronich
    Affiliations
    Department of Community Medicine and Epidemiology, Carmel Medical Center, Haifa 3436217, Israel

    The Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa 3200003, Israel
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  • Flavio Lejbkowicz
    Affiliations
    Department of Community Medicine and Epidemiology, Carmel Medical Center, Haifa 3436217, Israel
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  • Mila Pinchev
    Affiliations
    Department of Community Medicine and Epidemiology, Carmel Medical Center, Haifa 3436217, Israel
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  • Miriam J. Smith
    Affiliations
    Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester, UK

    Division of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK
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  • Anthony Howell
    Affiliations
    Division of Cancer Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK

    Nightingale/Prevent Breast Cancer Centre, Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, UK

    Manchester Breast Centre, Manchester Cancer Research Centre, The Christie Hospital, Manchester, UK
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  • William G. Newman
    Affiliations
    Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester, UK

    Division of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK
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  • Emma R. Woodward
    Affiliations
    Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester, UK

    Division of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK
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  • Elaine F. Harkness
    Affiliations
    Nightingale/Prevent Breast Cancer Centre, Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, UK

    Division of Informatics, Imaging & Data Sciences, School of Health Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK
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  • Adam R. Brentnall
    Affiliations
    Queen Mary University of London, Centre for Cancer Prevention, Wolfson Institute of Population Health, Charterhouse Square, London, UK
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  • Jack Cuzick
    Affiliations
    Queen Mary University of London, Centre for Cancer Prevention, Wolfson Institute of Population Health, Charterhouse Square, London, UK
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  • Gad Rennert
    Affiliations
    Department of Community Medicine and Epidemiology, Carmel Medical Center, Haifa 3436217, Israel

    The Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa 3200003, Israel
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  • Author Footnotes
    ∗ Equal contribution senior authors
    Sacha J. Howell
    Footnotes
    ∗ Equal contribution senior authors
    Affiliations
    Division of Cancer Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK

    Nightingale/Prevent Breast Cancer Centre, Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, UK

    Manchester Breast Centre, Manchester Cancer Research Centre, The Christie Hospital, Manchester, UK
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  • Author Footnotes
    ∗ Equal contribution senior authors
    D. Gareth Evans
    Correspondence
    Corresponding author: Professor D Gareth Evans, Genomic Medicine, MAHSC, St. Mary’s Hospital, Oxford Road, Manchester M13 9WL, UK; Phone +447710209810
    Footnotes
    ∗ Equal contribution senior authors
    Affiliations
    Division of Cancer Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK

    Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester, UK

    Division of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK

    Nightingale/Prevent Breast Cancer Centre, Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, UK

    Manchester Breast Centre, Manchester Cancer Research Centre, The Christie Hospital, Manchester, UK
    Search for articles by this author
  • Author Footnotes
    ∗ Equal contribution senior authors
Open AccessPublished:April 12, 2023DOI:https://doi.org/10.1016/j.gim.2023.100846
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      Abstract

      Purpose

      Polygenic risk scores (PRS) are a major component of accurate breast cancer (BC) risk prediction but require ethnicity-specific calibration. Ashkenazi-Jews-(AJ) are assumed to be of White-European-(WE) origin in some commercially-available PRS despite differing effect-allele-frequencies-(EAFs). We conducted a case-control study of WE and AJ women from the PROCAS-(Predicting-Risk-of-Cancer-at-Screening) study. The BCINIS-(Breast-Cancer-in-Northern-Israel-study) provided a separate AJ population-based case-control validation series.

      Methods

      All women underwent Illumina Oncoarray SNP-analysis. Two PRS were assessed, SNP142&SNP78. 221/2243 WE (Discovery:cases=111;controls=110;Validation:cases=651;controls=1772) and 221 AJ (cases=121;controls=110) women were included from the UK study; the Israeli series consisted of 2045 AJ women (cases=1331;controls=714). EAFs were obtained from gnomAD.

      Results

      In the UK study the mean SNP142PRS demonstrated good calibration and discrimination in WEs: mean PRS in cases=1.33-(95%CI=1.18-1.48) and controls=1.01-(95%CI=0.89-1.13). In AJs from Manchester, the mean PRS in cases=1.54-(1.38-1.70) and controls=1.20-(1.08-1.32) demonstrated good discrimination but overestimation of BC relative-risk. After adjusting for AJ EAFs, mean risk was corrected (mean SNP142-PRS cases=1.30-(95%CI=1.16-1.44) and controls=1.02-(95%CI=0.92-1.12)). This was recapitulated in the larger Israeli dataset with good discrimination (AUC=0.632-(95%CI=0.607-0.657) for SNP142).

      Conclusion

      AJ women should not be given BC relative-risk predictions based on PRS calibrated to EAFs from WEs. PRS need to be recalibrated using AJ-derived-EAFs. A simple recalibration using the mean PRS adjustment ratio likely performs well.

      Keywords