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The importance of ethnicity: Are breast cancer polygenic risk scores ready for women who are not of White European origin?

Polygenic risk scores (PRS) for disease risk stratification show great promise for application in general populations, but most are based on data from individuals of White European origin. We assessed two well validated PRS (SNP18, SNP143) in the Predicting‐Risk‐of‐Cancer‐At‐Screening (PROCAS) study...

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Autores principales: Evans, D. Gareth, van Veen, Elke M., Byers, Helen, Roberts, Eleanor, Howell, Anthony, Howell, Sacha J., Harkness, Elaine F., Brentnall, Adam, Cuzick, Jack, Newman, William G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290473/
https://www.ncbi.nlm.nih.gov/pubmed/34460111
http://dx.doi.org/10.1002/ijc.33782
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author Evans, D. Gareth
van Veen, Elke M.
Byers, Helen
Roberts, Eleanor
Howell, Anthony
Howell, Sacha J.
Harkness, Elaine F.
Brentnall, Adam
Cuzick, Jack
Newman, William G.
author_facet Evans, D. Gareth
van Veen, Elke M.
Byers, Helen
Roberts, Eleanor
Howell, Anthony
Howell, Sacha J.
Harkness, Elaine F.
Brentnall, Adam
Cuzick, Jack
Newman, William G.
author_sort Evans, D. Gareth
collection PubMed
description Polygenic risk scores (PRS) for disease risk stratification show great promise for application in general populations, but most are based on data from individuals of White European origin. We assessed two well validated PRS (SNP18, SNP143) in the Predicting‐Risk‐of‐Cancer‐At‐Screening (PROCAS) study in North‐West England for breast cancer prediction based on ethnicity. Overall, 9475 women without breast cancer at study entry, including 645 who subsequently developed invasive breast cancer or ductal carcinoma in situ provided DNA. All were genotyped for SNP18 and a subset of 1868 controls were genotyped for SNP143. For White Europeans both PRS discriminated well between individuals with and without cancer. For n = 395 Black (n = 112), Asian (n = 119), mixed (n = 44) or Jewish (n = 120) women without cancer both PRS overestimated breast cancer risk, being most marked for women of Black and Jewish origin (P < .001). SNP143 resulted in a potential mean 40% breast cancer risk overestimation in the combined group of non‐White/non‐European origin. SNP‐PRS that has been normalized based on White European ethnicity for breast cancer should not be used to predict risk in women of other ethnicities. There is an urgent need to develop PRS specific for other ethnicities, in order to widen access of this technology.
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spelling pubmed-92904732022-07-20 The importance of ethnicity: Are breast cancer polygenic risk scores ready for women who are not of White European origin? Evans, D. Gareth van Veen, Elke M. Byers, Helen Roberts, Eleanor Howell, Anthony Howell, Sacha J. Harkness, Elaine F. Brentnall, Adam Cuzick, Jack Newman, William G. Int J Cancer Cancer Genetics and Epigenetics Polygenic risk scores (PRS) for disease risk stratification show great promise for application in general populations, but most are based on data from individuals of White European origin. We assessed two well validated PRS (SNP18, SNP143) in the Predicting‐Risk‐of‐Cancer‐At‐Screening (PROCAS) study in North‐West England for breast cancer prediction based on ethnicity. Overall, 9475 women without breast cancer at study entry, including 645 who subsequently developed invasive breast cancer or ductal carcinoma in situ provided DNA. All were genotyped for SNP18 and a subset of 1868 controls were genotyped for SNP143. For White Europeans both PRS discriminated well between individuals with and without cancer. For n = 395 Black (n = 112), Asian (n = 119), mixed (n = 44) or Jewish (n = 120) women without cancer both PRS overestimated breast cancer risk, being most marked for women of Black and Jewish origin (P < .001). SNP143 resulted in a potential mean 40% breast cancer risk overestimation in the combined group of non‐White/non‐European origin. SNP‐PRS that has been normalized based on White European ethnicity for breast cancer should not be used to predict risk in women of other ethnicities. There is an urgent need to develop PRS specific for other ethnicities, in order to widen access of this technology. John Wiley & Sons, Inc. 2021-09-07 2022-01-01 /pmc/articles/PMC9290473/ /pubmed/34460111 http://dx.doi.org/10.1002/ijc.33782 Text en © 2021 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Cancer Genetics and Epigenetics
Evans, D. Gareth
van Veen, Elke M.
Byers, Helen
Roberts, Eleanor
Howell, Anthony
Howell, Sacha J.
Harkness, Elaine F.
Brentnall, Adam
Cuzick, Jack
Newman, William G.
The importance of ethnicity: Are breast cancer polygenic risk scores ready for women who are not of White European origin?
title The importance of ethnicity: Are breast cancer polygenic risk scores ready for women who are not of White European origin?
title_full The importance of ethnicity: Are breast cancer polygenic risk scores ready for women who are not of White European origin?
title_fullStr The importance of ethnicity: Are breast cancer polygenic risk scores ready for women who are not of White European origin?
title_full_unstemmed The importance of ethnicity: Are breast cancer polygenic risk scores ready for women who are not of White European origin?
title_short The importance of ethnicity: Are breast cancer polygenic risk scores ready for women who are not of White European origin?
title_sort importance of ethnicity: are breast cancer polygenic risk scores ready for women who are not of white european origin?
topic Cancer Genetics and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290473/
https://www.ncbi.nlm.nih.gov/pubmed/34460111
http://dx.doi.org/10.1002/ijc.33782
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