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Establishment and validation of serum lipid-based nomogram for predicting the risk of prostate cancer

BACKGROUND: This study aimed to explore the value of combined serum lipids with clinical symptoms to diagnose prostate cancer (PCa), and to develop and validate a Nomogram and prediction model to better select patients at risk of PCa for prostate biopsy. METHODS: Retrospective analysis of 548 patien...

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Autores principales: Feng, Fu, Zhong, Yu-Xiang, Chen, Yang, Lin, Fu-Xiang, Huang, Jian-Hua, Mai, Yuan, Zhao, Peng-Peng, Wei, Wei, Zhu, Hua-Cai, Xu, Zhan-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349516/
https://www.ncbi.nlm.nih.gov/pubmed/37452418
http://dx.doi.org/10.1186/s12894-023-01291-w
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author Feng, Fu
Zhong, Yu-Xiang
Chen, Yang
Lin, Fu-Xiang
Huang, Jian-Hua
Mai, Yuan
Zhao, Peng-Peng
Wei, Wei
Zhu, Hua-Cai
Xu, Zhan-Ping
author_facet Feng, Fu
Zhong, Yu-Xiang
Chen, Yang
Lin, Fu-Xiang
Huang, Jian-Hua
Mai, Yuan
Zhao, Peng-Peng
Wei, Wei
Zhu, Hua-Cai
Xu, Zhan-Ping
author_sort Feng, Fu
collection PubMed
description BACKGROUND: This study aimed to explore the value of combined serum lipids with clinical symptoms to diagnose prostate cancer (PCa), and to develop and validate a Nomogram and prediction model to better select patients at risk of PCa for prostate biopsy. METHODS: Retrospective analysis of 548 patients who underwent prostate biopsies as a result of high serum prostate-specific antigen (PSA) levels or irregular digital rectal examinations (DRE) was conducted. The enrolled patients were randomly assigned to the training groups (n = 384, 70%) and validation groups (n = 164, 30%). To identify independent variables for PCa, serum lipids (TC, TG, HDL, LDL, apoA-1, and apoB) were taken into account in the multivariable logistic regression analyses of the training group, and established predictive models. After that, we evaluated prediction models with clinical markers using decision curves and the area under the curve (AUC). Based on training group data, a Nomogram was developed to predict PCa. RESULTS: 210 (54.70%) of the patients in the training group were diagnosed with PCa. Multivariate regression analysis showed that total PSA, f/tPSA, PSA density (PSAD), TG, LDL, DRE, and TRUS were independent risk predictors of PCa. A prediction model utilizing a Nomogram was constructed with a cut-off value of 0.502. The training and validation groups achieved area under the curve (AUC) values of 0.846 and 0.814 respectively. According to the decision curve analysis (DCA), the prediction model yielded optimal overall net benefits in both the training and validation groups, which is better than the optimal net benefit of PSA alone. After comparing our developed prediction model with two domestic models and PCPT-RC, we found that our prediction model exhibited significantly superior predictive performance. Furthermore, in comparison with clinical indicators, our Nomogram’s ability to predict prostate cancer showed good estimation, suggesting its potential as a reliable tool for prognostication. CONCLUSIONS: The prediction model and Nomogram, which utilize both blood lipid levels and clinical signs, demonstrated improved accuracy in predicting the risk of prostate cancer, and consequently can guide the selection of appropriate diagnostic strategies for each patient in a more personalized manner. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12894-023-01291-w.
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spelling pubmed-103495162023-07-16 Establishment and validation of serum lipid-based nomogram for predicting the risk of prostate cancer Feng, Fu Zhong, Yu-Xiang Chen, Yang Lin, Fu-Xiang Huang, Jian-Hua Mai, Yuan Zhao, Peng-Peng Wei, Wei Zhu, Hua-Cai Xu, Zhan-Ping BMC Urol Research BACKGROUND: This study aimed to explore the value of combined serum lipids with clinical symptoms to diagnose prostate cancer (PCa), and to develop and validate a Nomogram and prediction model to better select patients at risk of PCa for prostate biopsy. METHODS: Retrospective analysis of 548 patients who underwent prostate biopsies as a result of high serum prostate-specific antigen (PSA) levels or irregular digital rectal examinations (DRE) was conducted. The enrolled patients were randomly assigned to the training groups (n = 384, 70%) and validation groups (n = 164, 30%). To identify independent variables for PCa, serum lipids (TC, TG, HDL, LDL, apoA-1, and apoB) were taken into account in the multivariable logistic regression analyses of the training group, and established predictive models. After that, we evaluated prediction models with clinical markers using decision curves and the area under the curve (AUC). Based on training group data, a Nomogram was developed to predict PCa. RESULTS: 210 (54.70%) of the patients in the training group were diagnosed with PCa. Multivariate regression analysis showed that total PSA, f/tPSA, PSA density (PSAD), TG, LDL, DRE, and TRUS were independent risk predictors of PCa. A prediction model utilizing a Nomogram was constructed with a cut-off value of 0.502. The training and validation groups achieved area under the curve (AUC) values of 0.846 and 0.814 respectively. According to the decision curve analysis (DCA), the prediction model yielded optimal overall net benefits in both the training and validation groups, which is better than the optimal net benefit of PSA alone. After comparing our developed prediction model with two domestic models and PCPT-RC, we found that our prediction model exhibited significantly superior predictive performance. Furthermore, in comparison with clinical indicators, our Nomogram’s ability to predict prostate cancer showed good estimation, suggesting its potential as a reliable tool for prognostication. CONCLUSIONS: The prediction model and Nomogram, which utilize both blood lipid levels and clinical signs, demonstrated improved accuracy in predicting the risk of prostate cancer, and consequently can guide the selection of appropriate diagnostic strategies for each patient in a more personalized manner. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12894-023-01291-w. BioMed Central 2023-07-14 /pmc/articles/PMC10349516/ /pubmed/37452418 http://dx.doi.org/10.1186/s12894-023-01291-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Feng, Fu
Zhong, Yu-Xiang
Chen, Yang
Lin, Fu-Xiang
Huang, Jian-Hua
Mai, Yuan
Zhao, Peng-Peng
Wei, Wei
Zhu, Hua-Cai
Xu, Zhan-Ping
Establishment and validation of serum lipid-based nomogram for predicting the risk of prostate cancer
title Establishment and validation of serum lipid-based nomogram for predicting the risk of prostate cancer
title_full Establishment and validation of serum lipid-based nomogram for predicting the risk of prostate cancer
title_fullStr Establishment and validation of serum lipid-based nomogram for predicting the risk of prostate cancer
title_full_unstemmed Establishment and validation of serum lipid-based nomogram for predicting the risk of prostate cancer
title_short Establishment and validation of serum lipid-based nomogram for predicting the risk of prostate cancer
title_sort establishment and validation of serum lipid-based nomogram for predicting the risk of prostate cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349516/
https://www.ncbi.nlm.nih.gov/pubmed/37452418
http://dx.doi.org/10.1186/s12894-023-01291-w
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