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Development and validation of a machine learning-based nomogram for predicting HLA-B27 expression
BACKGROUND: HLA-B27 positivity is normal in patients undergoing rheumatic diseases. The diagnosis of many diseases requires an HLA-B27 examination. METHODS: This study screened totally 1503 patients who underwent HLA-B27 examination, liver/kidney function tests, and complete blood routine examinatio...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521518/ https://www.ncbi.nlm.nih.gov/pubmed/37752439 http://dx.doi.org/10.1186/s12865-023-00566-z |
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author | Zhu, Jichong Tan, Weiming Zhan, Xinli Lu, Qing Liang, Tuo JieJiang Li, Hao Zhou, Chenxing Wu, Shaofeng Chen, Tianyou Yao, Yuanlin Liao, Shian Yu, Chaojie Chen, Liyi Liu, Chong |
author_facet | Zhu, Jichong Tan, Weiming Zhan, Xinli Lu, Qing Liang, Tuo JieJiang Li, Hao Zhou, Chenxing Wu, Shaofeng Chen, Tianyou Yao, Yuanlin Liao, Shian Yu, Chaojie Chen, Liyi Liu, Chong |
author_sort | Zhu, Jichong |
collection | PubMed |
description | BACKGROUND: HLA-B27 positivity is normal in patients undergoing rheumatic diseases. The diagnosis of many diseases requires an HLA-B27 examination. METHODS: This study screened totally 1503 patients who underwent HLA-B27 examination, liver/kidney function tests, and complete blood routine examination in First Affiliated Hospital of Guangxi Medical University. The training cohort included 509 cases with HLA-B27 positivity whereas 611 with HLA-B27 negativity. In addition, validation cohort included 147 cases with HLA-B27 positivity whereas 236 with HLA-B27 negativity. In this study, 3 ML approaches, namely, LASSO, support vector machine (SVM) recursive feature elimination and random forest, were adopted for screening feature variables. Subsequently, to acquire the prediction model, the intersection was selected. Finally, differences among 148 cases with HLA-B27 positivity and negativity suffering from ankylosing spondylitis (AS) were investigated. RESULTS: Six factors, namely red blood cell count, human major compatibility complex, mean platelet volume, albumin/globulin ratio (ALB/GLB), prealbumin, and bicarbonate radical, were chosen with the aim of constructing the diagnostic nomogram using ML methods. For training queue, nomogram curve exhibited the value of area under the curve (AUC) of 0.8254496, and C-value of the model was 0.825. Moreover, nomogram C-value of the validation queue was 0.853, and the AUC value was 0.852675. Furthermore, a significant decrease in the ALB/GLB was noted among cases with HLA-B27 positivity and AS cases. CONCLUSION: To conclude, the proposed ML model can effectively predict HLA-B27 and help doctors in the diagnosis of various immune diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12865-023-00566-z. |
format | Online Article Text |
id | pubmed-10521518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105215182023-09-27 Development and validation of a machine learning-based nomogram for predicting HLA-B27 expression Zhu, Jichong Tan, Weiming Zhan, Xinli Lu, Qing Liang, Tuo JieJiang Li, Hao Zhou, Chenxing Wu, Shaofeng Chen, Tianyou Yao, Yuanlin Liao, Shian Yu, Chaojie Chen, Liyi Liu, Chong BMC Immunol Research BACKGROUND: HLA-B27 positivity is normal in patients undergoing rheumatic diseases. The diagnosis of many diseases requires an HLA-B27 examination. METHODS: This study screened totally 1503 patients who underwent HLA-B27 examination, liver/kidney function tests, and complete blood routine examination in First Affiliated Hospital of Guangxi Medical University. The training cohort included 509 cases with HLA-B27 positivity whereas 611 with HLA-B27 negativity. In addition, validation cohort included 147 cases with HLA-B27 positivity whereas 236 with HLA-B27 negativity. In this study, 3 ML approaches, namely, LASSO, support vector machine (SVM) recursive feature elimination and random forest, were adopted for screening feature variables. Subsequently, to acquire the prediction model, the intersection was selected. Finally, differences among 148 cases with HLA-B27 positivity and negativity suffering from ankylosing spondylitis (AS) were investigated. RESULTS: Six factors, namely red blood cell count, human major compatibility complex, mean platelet volume, albumin/globulin ratio (ALB/GLB), prealbumin, and bicarbonate radical, were chosen with the aim of constructing the diagnostic nomogram using ML methods. For training queue, nomogram curve exhibited the value of area under the curve (AUC) of 0.8254496, and C-value of the model was 0.825. Moreover, nomogram C-value of the validation queue was 0.853, and the AUC value was 0.852675. Furthermore, a significant decrease in the ALB/GLB was noted among cases with HLA-B27 positivity and AS cases. CONCLUSION: To conclude, the proposed ML model can effectively predict HLA-B27 and help doctors in the diagnosis of various immune diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12865-023-00566-z. BioMed Central 2023-09-26 /pmc/articles/PMC10521518/ /pubmed/37752439 http://dx.doi.org/10.1186/s12865-023-00566-z 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 Zhu, Jichong Tan, Weiming Zhan, Xinli Lu, Qing Liang, Tuo JieJiang Li, Hao Zhou, Chenxing Wu, Shaofeng Chen, Tianyou Yao, Yuanlin Liao, Shian Yu, Chaojie Chen, Liyi Liu, Chong Development and validation of a machine learning-based nomogram for predicting HLA-B27 expression |
title | Development and validation of a machine learning-based nomogram for predicting HLA-B27 expression |
title_full | Development and validation of a machine learning-based nomogram for predicting HLA-B27 expression |
title_fullStr | Development and validation of a machine learning-based nomogram for predicting HLA-B27 expression |
title_full_unstemmed | Development and validation of a machine learning-based nomogram for predicting HLA-B27 expression |
title_short | Development and validation of a machine learning-based nomogram for predicting HLA-B27 expression |
title_sort | development and validation of a machine learning-based nomogram for predicting hla-b27 expression |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521518/ https://www.ncbi.nlm.nih.gov/pubmed/37752439 http://dx.doi.org/10.1186/s12865-023-00566-z |
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