Cargando…

Evaluation of a Multiethnic Polygenic Risk Score Model for Prostate Cancer

Polygenic risk scores (PRSs) of common genetic variants have shown promise in prostate cancer risk stratification, but their validity across populations has yet to be confirmed. We evaluated a multiethnic PRS model based on 269 germline genetic risk variants (261 were available for analysis) using a...

Descripción completa

Detalles Bibliográficos
Autores principales: Plym, Anna, Penney, Kathryn L, Kalia, Sarah, Kraft, Peter, Conti, David V, Haiman, Christopher, Mucci, Lorelei A, Kibel, Adam S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086757/
https://www.ncbi.nlm.nih.gov/pubmed/33792693
http://dx.doi.org/10.1093/jnci/djab058
_version_ 1784704075755945984
author Plym, Anna
Penney, Kathryn L
Kalia, Sarah
Kraft, Peter
Conti, David V
Haiman, Christopher
Mucci, Lorelei A
Kibel, Adam S
author_facet Plym, Anna
Penney, Kathryn L
Kalia, Sarah
Kraft, Peter
Conti, David V
Haiman, Christopher
Mucci, Lorelei A
Kibel, Adam S
author_sort Plym, Anna
collection PubMed
description Polygenic risk scores (PRSs) of common genetic variants have shown promise in prostate cancer risk stratification, but their validity across populations has yet to be confirmed. We evaluated a multiethnic PRS model based on 269 germline genetic risk variants (261 were available for analysis) using an independent population of 13 628 US men. The PRS was strongly associated with prostate cancer but not with any other disease. Comparing men in the top PRS decile with those at average risk (40%-60%), the odds ratio of prostate cancer was 3.89 (95% confidence interval = 3.24 to 4.68) for men of European ancestry and 3.81 (95% confidence interval = 1.48 to 10.19) for men of African ancestry. By age 85 years, the cumulative incidence of prostate cancer for European American men was 7.1% in the bottom decile and 54.1% in the top decile. This suggests that the PRS can be used to identify a substantial proportion of men at high risk for prostate cancer.
format Online
Article
Text
id pubmed-9086757
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-90867572022-05-11 Evaluation of a Multiethnic Polygenic Risk Score Model for Prostate Cancer Plym, Anna Penney, Kathryn L Kalia, Sarah Kraft, Peter Conti, David V Haiman, Christopher Mucci, Lorelei A Kibel, Adam S J Natl Cancer Inst Brief Communications Polygenic risk scores (PRSs) of common genetic variants have shown promise in prostate cancer risk stratification, but their validity across populations has yet to be confirmed. We evaluated a multiethnic PRS model based on 269 germline genetic risk variants (261 were available for analysis) using an independent population of 13 628 US men. The PRS was strongly associated with prostate cancer but not with any other disease. Comparing men in the top PRS decile with those at average risk (40%-60%), the odds ratio of prostate cancer was 3.89 (95% confidence interval = 3.24 to 4.68) for men of European ancestry and 3.81 (95% confidence interval = 1.48 to 10.19) for men of African ancestry. By age 85 years, the cumulative incidence of prostate cancer for European American men was 7.1% in the bottom decile and 54.1% in the top decile. This suggests that the PRS can be used to identify a substantial proportion of men at high risk for prostate cancer. Oxford University Press 2021-04-01 /pmc/articles/PMC9086757/ /pubmed/33792693 http://dx.doi.org/10.1093/jnci/djab058 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Brief Communications
Plym, Anna
Penney, Kathryn L
Kalia, Sarah
Kraft, Peter
Conti, David V
Haiman, Christopher
Mucci, Lorelei A
Kibel, Adam S
Evaluation of a Multiethnic Polygenic Risk Score Model for Prostate Cancer
title Evaluation of a Multiethnic Polygenic Risk Score Model for Prostate Cancer
title_full Evaluation of a Multiethnic Polygenic Risk Score Model for Prostate Cancer
title_fullStr Evaluation of a Multiethnic Polygenic Risk Score Model for Prostate Cancer
title_full_unstemmed Evaluation of a Multiethnic Polygenic Risk Score Model for Prostate Cancer
title_short Evaluation of a Multiethnic Polygenic Risk Score Model for Prostate Cancer
title_sort evaluation of a multiethnic polygenic risk score model for prostate cancer
topic Brief Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086757/
https://www.ncbi.nlm.nih.gov/pubmed/33792693
http://dx.doi.org/10.1093/jnci/djab058
work_keys_str_mv AT plymanna evaluationofamultiethnicpolygenicriskscoremodelforprostatecancer
AT penneykathrynl evaluationofamultiethnicpolygenicriskscoremodelforprostatecancer
AT kaliasarah evaluationofamultiethnicpolygenicriskscoremodelforprostatecancer
AT kraftpeter evaluationofamultiethnicpolygenicriskscoremodelforprostatecancer
AT contidavidv evaluationofamultiethnicpolygenicriskscoremodelforprostatecancer
AT haimanchristopher evaluationofamultiethnicpolygenicriskscoremodelforprostatecancer
AT mucciloreleia evaluationofamultiethnicpolygenicriskscoremodelforprostatecancer
AT kibeladams evaluationofamultiethnicpolygenicriskscoremodelforprostatecancer