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

被引:2
|
作者
Roberts, Eleanor [2 ]
van Veen, Elke M. [3 ,4 ]
Byers, Helen [3 ,4 ]
Barnett-Griness, Ofra [5 ]
Gronich, Naomi [5 ,6 ]
Lejbkowicz, Flavio [5 ]
Pinchev, Mila [5 ]
Smith, Miriam J. [3 ,4 ]
Howell, Anthony [2 ,7 ,8 ]
Newman, William G. [3 ,4 ]
Woodward, Emma R. [3 ,4 ]
Harkness, Elaine F. [7 ,9 ]
Brentnall, Adam R. [10 ]
Cuzick, Jack [10 ]
Rennert, Gad [5 ,6 ]
Howell, Sacha J. [2 ,7 ,8 ]
Evans, D. . Gareth [1 ,2 ,3 ,4 ,7 ,8 ]
机构
[1] St Marys Hosp, Genom Med, MAHSC, Oxford Rd, Manchester M13 9WL, England
[2] Univ Manchester, Fac Biol Med & Hlth, Manchester Acad Hlth Sci Ctr, Div Canc Sci, Manchester, England
[3] Manchester Univ Hosp NHS Fdn Trust, Manchester Ctr Genom Med, Manchester, England
[4] Univ Manchester, Fac Biol Med & Hlth, Manchester Acad Hlth Sci Ctr, Sch Biol Sci,Div Evolut Infecti & Genom, Manchester, England
[5] Carmel Hosp, Dept Community Med & Epidemiol, Haifa, Israel
[6] Technion Israel Inst Technol, Ruth & Bruce Rappaport Fac Med, Haifa, Israel
[7] Manchester Univ NHS Fdn Trust, Wythenshawe Hosp, Nightingale Prevent Breast Canc Ctr, Manchester, England
[8] Christie Hosp, Manchester Breast Ctr, Manchester Canc Res Ctr, Manchester, England
[9] Univ Manchester, Fac Biol Med & Hlth, Sch Hlth Sci, Div Informat Imaging & Data Sci, Manchester, England
[10] Queen Mary Univ London, Wolfson Inst Populat Hlth, Ctr Canc Prevent, Charterhouse Sq, London, England
关键词
Ashkenazi Jewish; Breast cancer; Early detection; Ethnicities; Polygenic risk scores; ANCESTRY;
D O I
10.1016/j.gim.2023.100846
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose: Polygenic risk scores (PRSs) are a major component of accurate breast cancer (BC) risk prediction but require ethnicity-specific calibration. Ashkenazi Jewish (AJ) population is assumed to be of White European (WE) origin in some commercially available PRSs despite differing effect allele frequencies (EAFs). We conducted a case-control study of WE and AJ women from the Predicting Risk of Cancer at Screening Study. The Breast Cancer in Northern Israel Study provided a separate AJ population-based case-control validation series. Methods: All women underwent Illumina OncoArray single-nucleotide variation (SNV; formerly single-nucleotide polymorphism [SNP]) analysis. Two PRSs were assessed, SNV142 and SNV78. A total of 221 of 2243 WE women (discovery: cases = 111; controls = 110; validation: cases = 651; controls = 1772) and 221 AJ women (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 the Genome Aggregation Database. Results: In the UK study, the mean SNV142 PRS demonstrated good calibration and discrimination in WE population, with mean PRS of 1.33 (95% CI 1.18-1.48) in cases and 1.01 (95% CI 0.89-1.13) in controls. In AJ women from Manchester, the mean PRS of 1.54 (1.38-1.70) in cases and 1.20 (1.081.32) in controls demonstrated good discrimination but overestimation of BC relative risk. After adjusting for EAFs for the AJ population, mean risk was corrected (mean SNV142 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 data set with good discrimination (area under the curve = 0.632 [95% CI 0.607-0.657] for SNV142). Conclusion: AJ women should not be given BC relative risk predictions based on PRSs calibrated to EAFs from the WE population. PRSs need to be recalibrated using AJ-derived EAFs. A simple recalibration using the mean PRS adjustment ratio likely performs well. & COPY; 2023 The Authors. Published by Elsevier Inc. on behalf of American College of Medical Genetics and Genomics. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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页数:9
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