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Prediction of cardiovascular disease risk based on major contributing features

The risk of cardiovascular disease (CVD) is a serious health threat to human society worldwide. The use of machine learning methods to predict the risk of CVD is of great relevance to identify high-risk patients and take timely interventions. In this study, we propose the XGBH machine learning model...

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Autores principales: Peng, Mengxiao, Hou, Fan, Cheng, Zhixiang, Shen, Tongtong, Liu, Kaixian, Zhao, Cai, Zheng, Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036320/
https://www.ncbi.nlm.nih.gov/pubmed/36959459
http://dx.doi.org/10.1038/s41598-023-31870-8
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author Peng, Mengxiao
Hou, Fan
Cheng, Zhixiang
Shen, Tongtong
Liu, Kaixian
Zhao, Cai
Zheng, Wen
author_facet Peng, Mengxiao
Hou, Fan
Cheng, Zhixiang
Shen, Tongtong
Liu, Kaixian
Zhao, Cai
Zheng, Wen
author_sort Peng, Mengxiao
collection PubMed
description The risk of cardiovascular disease (CVD) is a serious health threat to human society worldwide. The use of machine learning methods to predict the risk of CVD is of great relevance to identify high-risk patients and take timely interventions. In this study, we propose the XGBH machine learning model, which is a CVD risk prediction model based on key contributing features. In this paper, the generalisation of the model was enhanced by adding retrospective data of 14,832 Chinese Shanxi CVD patients to the kaggle dataset. The XGBH risk prediction model proposed in this paper was validated to be highly accurate (AUC = 0.81) compared to the baseline risk score (AUC = 0.65), and the accuracy of the model for CVD risk prediction was improved with the inclusion of the conventional biometric BMI variable. To increase the clinical application of the model, a simpler diagnostic model was designed in this paper, which requires only three characteristics from the patient (age, value of systolic blood pressure and whether cholesterol is normal or not) to enable early intervention in the treatment of high-risk patients with a slight reduction in accuracy (AUC = 0.79). Ultimately, a CVD risk score model with few features and high accuracy will be established based on the main contributing features. Of course, further prospective studies, as well as studies with other populations, are needed to assess the actual clinical effectiveness of the XGBH risk prediction model.
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spelling pubmed-100363202023-03-25 Prediction of cardiovascular disease risk based on major contributing features Peng, Mengxiao Hou, Fan Cheng, Zhixiang Shen, Tongtong Liu, Kaixian Zhao, Cai Zheng, Wen Sci Rep Article The risk of cardiovascular disease (CVD) is a serious health threat to human society worldwide. The use of machine learning methods to predict the risk of CVD is of great relevance to identify high-risk patients and take timely interventions. In this study, we propose the XGBH machine learning model, which is a CVD risk prediction model based on key contributing features. In this paper, the generalisation of the model was enhanced by adding retrospective data of 14,832 Chinese Shanxi CVD patients to the kaggle dataset. The XGBH risk prediction model proposed in this paper was validated to be highly accurate (AUC = 0.81) compared to the baseline risk score (AUC = 0.65), and the accuracy of the model for CVD risk prediction was improved with the inclusion of the conventional biometric BMI variable. To increase the clinical application of the model, a simpler diagnostic model was designed in this paper, which requires only three characteristics from the patient (age, value of systolic blood pressure and whether cholesterol is normal or not) to enable early intervention in the treatment of high-risk patients with a slight reduction in accuracy (AUC = 0.79). Ultimately, a CVD risk score model with few features and high accuracy will be established based on the main contributing features. Of course, further prospective studies, as well as studies with other populations, are needed to assess the actual clinical effectiveness of the XGBH risk prediction model. Nature Publishing Group UK 2023-03-23 /pmc/articles/PMC10036320/ /pubmed/36959459 http://dx.doi.org/10.1038/s41598-023-31870-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) .
spellingShingle Article
Peng, Mengxiao
Hou, Fan
Cheng, Zhixiang
Shen, Tongtong
Liu, Kaixian
Zhao, Cai
Zheng, Wen
Prediction of cardiovascular disease risk based on major contributing features
title Prediction of cardiovascular disease risk based on major contributing features
title_full Prediction of cardiovascular disease risk based on major contributing features
title_fullStr Prediction of cardiovascular disease risk based on major contributing features
title_full_unstemmed Prediction of cardiovascular disease risk based on major contributing features
title_short Prediction of cardiovascular disease risk based on major contributing features
title_sort prediction of cardiovascular disease risk based on major contributing features
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036320/
https://www.ncbi.nlm.nih.gov/pubmed/36959459
http://dx.doi.org/10.1038/s41598-023-31870-8
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