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Early prediction of prostate cancer risk in younger men using polygenic risk scores and electronic health records
BACKGROUND: Prostate cancer (PCa) screening is not routinely conducted in men aged 55 and younger, although this age group accounts for more than 10% of cases. Polygenic risk scores (PRSs) and patient data applied toward early prediction of PCa may lead to earlier interventions and increased surviva...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9844630/ https://www.ncbi.nlm.nih.gov/pubmed/35751453 http://dx.doi.org/10.1002/cam4.4934 |
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author | Varma, Amita Maharjan, Jenish Garikipati, Anurag Hurtado, Myrna Shokouhi, Sepideh Mao, Qingqing |
author_facet | Varma, Amita Maharjan, Jenish Garikipati, Anurag Hurtado, Myrna Shokouhi, Sepideh Mao, Qingqing |
author_sort | Varma, Amita |
collection | PubMed |
description | BACKGROUND: Prostate cancer (PCa) screening is not routinely conducted in men aged 55 and younger, although this age group accounts for more than 10% of cases. Polygenic risk scores (PRSs) and patient data applied toward early prediction of PCa may lead to earlier interventions and increased survival. We have developed machine learning (ML) models to predict PCa risk in men 55 and under using PRSs combined with patient data. METHODS: We conducted a retrospective study on 91,106 male patients aged 35–55 using the UK Biobank database. Five gradient boosting models were developed and validated utilizing routine screening data, PRSs, additional clinical data, or combinations of the three. RESULTS: Combinations of PRSs and patient data outperformed models that utilized PRS or patient data only, and the highest performing models achieved an area under the receiver operating characteristic curve of 0.788. Our models demonstrated a substantially lower false positive rate (35.4%) in comparison to standard screening using prostate‐specific antigen (60%–67%). CONCLUSION: This study provides the first preliminary evidence for the use of PRSs with patient data in a ML algorithm for PCa risk prediction in men aged 55 and under for whom screening is not standard practice. |
format | Online Article Text |
id | pubmed-9844630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98446302023-01-24 Early prediction of prostate cancer risk in younger men using polygenic risk scores and electronic health records Varma, Amita Maharjan, Jenish Garikipati, Anurag Hurtado, Myrna Shokouhi, Sepideh Mao, Qingqing Cancer Med RESEARCH ARTICLES BACKGROUND: Prostate cancer (PCa) screening is not routinely conducted in men aged 55 and younger, although this age group accounts for more than 10% of cases. Polygenic risk scores (PRSs) and patient data applied toward early prediction of PCa may lead to earlier interventions and increased survival. We have developed machine learning (ML) models to predict PCa risk in men 55 and under using PRSs combined with patient data. METHODS: We conducted a retrospective study on 91,106 male patients aged 35–55 using the UK Biobank database. Five gradient boosting models were developed and validated utilizing routine screening data, PRSs, additional clinical data, or combinations of the three. RESULTS: Combinations of PRSs and patient data outperformed models that utilized PRS or patient data only, and the highest performing models achieved an area under the receiver operating characteristic curve of 0.788. Our models demonstrated a substantially lower false positive rate (35.4%) in comparison to standard screening using prostate‐specific antigen (60%–67%). CONCLUSION: This study provides the first preliminary evidence for the use of PRSs with patient data in a ML algorithm for PCa risk prediction in men aged 55 and under for whom screening is not standard practice. John Wiley and Sons Inc. 2022-06-25 /pmc/articles/PMC9844630/ /pubmed/35751453 http://dx.doi.org/10.1002/cam4.4934 Text en © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RESEARCH ARTICLES Varma, Amita Maharjan, Jenish Garikipati, Anurag Hurtado, Myrna Shokouhi, Sepideh Mao, Qingqing Early prediction of prostate cancer risk in younger men using polygenic risk scores and electronic health records |
title | Early prediction of prostate cancer risk in younger men using polygenic risk scores and electronic health records |
title_full | Early prediction of prostate cancer risk in younger men using polygenic risk scores and electronic health records |
title_fullStr | Early prediction of prostate cancer risk in younger men using polygenic risk scores and electronic health records |
title_full_unstemmed | Early prediction of prostate cancer risk in younger men using polygenic risk scores and electronic health records |
title_short | Early prediction of prostate cancer risk in younger men using polygenic risk scores and electronic health records |
title_sort | early prediction of prostate cancer risk in younger men using polygenic risk scores and electronic health records |
topic | RESEARCH ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9844630/ https://www.ncbi.nlm.nih.gov/pubmed/35751453 http://dx.doi.org/10.1002/cam4.4934 |
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