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A Comparison of XGBoost, Random Forest, and Nomograph for the Prediction of Disease Severity in Patients With COVID-19 Pneumonia: Implications of Cytokine and Immune Cell Profile
BACKGROUND AND AIMS: The aim of this study was to apply machine learning models and a nomogram to differentiate critically ill from non-critically ill COVID-19 pneumonia patients. METHODS: Clinical symptoms and signs, laboratory parameters, cytokine profile, and immune cellular data of 63 COVID-19 p...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039730/ https://www.ncbi.nlm.nih.gov/pubmed/35493729 http://dx.doi.org/10.3389/fcimb.2022.819267 |
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author | Hong, Wandong Zhou, Xiaoying Jin, Shengchun Lu, Yajing Pan, Jingyi Lin, Qingyi Yang, Shaopeng Xu, Tingting Basharat, Zarrin Zippi, Maddalena Fiorino, Sirio Tsukanov, Vladislav Stock, Simon Grottesi, Alfonso Chen, Qin Pan, Jingye |
author_facet | Hong, Wandong Zhou, Xiaoying Jin, Shengchun Lu, Yajing Pan, Jingyi Lin, Qingyi Yang, Shaopeng Xu, Tingting Basharat, Zarrin Zippi, Maddalena Fiorino, Sirio Tsukanov, Vladislav Stock, Simon Grottesi, Alfonso Chen, Qin Pan, Jingye |
author_sort | Hong, Wandong |
collection | PubMed |
description | BACKGROUND AND AIMS: The aim of this study was to apply machine learning models and a nomogram to differentiate critically ill from non-critically ill COVID-19 pneumonia patients. METHODS: Clinical symptoms and signs, laboratory parameters, cytokine profile, and immune cellular data of 63 COVID-19 pneumonia patients were retrospectively reviewed. Outcomes were followed up until Mar 12, 2020. A logistic regression function (LR model), Random Forest, and XGBoost models were developed. The performance of these models was measured by area under receiver operating characteristic curve (AUC) analysis. RESULTS: Univariate analysis revealed that there was a difference between critically and non-critically ill patients with respect to levels of interleukin-6, interleukin-10, T cells, CD4(+) T, and CD8(+) T cells. Interleukin-10 with an AUC of 0.86 was most useful predictor of critically ill patients with COVID-19 pneumonia. Ten variables (respiratory rate, neutrophil counts, aspartate transaminase, albumin, serum procalcitonin, D-dimer and B-type natriuretic peptide, CD4(+) T cells, interleukin-6 and interleukin-10) were used as candidate predictors for LR model, Random Forest (RF) and XGBoost model application. The coefficients from LR model were utilized to build a nomogram. RF and XGBoost methods suggested that Interleukin-10 and interleukin-6 were the most important variables for severity of illness prediction. The mean AUC for LR, RF, and XGBoost model were 0.91, 0.89, and 0.93 respectively (in two-fold cross-validation). Individualized prediction by XGBoost model was explained by local interpretable model-agnostic explanations (LIME) plot. CONCLUSIONS: XGBoost exhibited the highest discriminatory performance for prediction of critically ill patients with COVID-19 pneumonia. It is inferred that the nomogram and visualized interpretation with LIME plot could be useful in the clinical setting. Additionally, interleukin-10 could serve as a useful predictor of critically ill patients with COVID-19 pneumonia. |
format | Online Article Text |
id | pubmed-9039730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90397302022-04-27 A Comparison of XGBoost, Random Forest, and Nomograph for the Prediction of Disease Severity in Patients With COVID-19 Pneumonia: Implications of Cytokine and Immune Cell Profile Hong, Wandong Zhou, Xiaoying Jin, Shengchun Lu, Yajing Pan, Jingyi Lin, Qingyi Yang, Shaopeng Xu, Tingting Basharat, Zarrin Zippi, Maddalena Fiorino, Sirio Tsukanov, Vladislav Stock, Simon Grottesi, Alfonso Chen, Qin Pan, Jingye Front Cell Infect Microbiol Cellular and Infection Microbiology BACKGROUND AND AIMS: The aim of this study was to apply machine learning models and a nomogram to differentiate critically ill from non-critically ill COVID-19 pneumonia patients. METHODS: Clinical symptoms and signs, laboratory parameters, cytokine profile, and immune cellular data of 63 COVID-19 pneumonia patients were retrospectively reviewed. Outcomes were followed up until Mar 12, 2020. A logistic regression function (LR model), Random Forest, and XGBoost models were developed. The performance of these models was measured by area under receiver operating characteristic curve (AUC) analysis. RESULTS: Univariate analysis revealed that there was a difference between critically and non-critically ill patients with respect to levels of interleukin-6, interleukin-10, T cells, CD4(+) T, and CD8(+) T cells. Interleukin-10 with an AUC of 0.86 was most useful predictor of critically ill patients with COVID-19 pneumonia. Ten variables (respiratory rate, neutrophil counts, aspartate transaminase, albumin, serum procalcitonin, D-dimer and B-type natriuretic peptide, CD4(+) T cells, interleukin-6 and interleukin-10) were used as candidate predictors for LR model, Random Forest (RF) and XGBoost model application. The coefficients from LR model were utilized to build a nomogram. RF and XGBoost methods suggested that Interleukin-10 and interleukin-6 were the most important variables for severity of illness prediction. The mean AUC for LR, RF, and XGBoost model were 0.91, 0.89, and 0.93 respectively (in two-fold cross-validation). Individualized prediction by XGBoost model was explained by local interpretable model-agnostic explanations (LIME) plot. CONCLUSIONS: XGBoost exhibited the highest discriminatory performance for prediction of critically ill patients with COVID-19 pneumonia. It is inferred that the nomogram and visualized interpretation with LIME plot could be useful in the clinical setting. Additionally, interleukin-10 could serve as a useful predictor of critically ill patients with COVID-19 pneumonia. Frontiers Media S.A. 2022-04-12 /pmc/articles/PMC9039730/ /pubmed/35493729 http://dx.doi.org/10.3389/fcimb.2022.819267 Text en Copyright © 2022 Hong, Zhou, Jin, Lu, Pan, Lin, Yang, Xu, Basharat, Zippi, Fiorino, Tsukanov, Stock, Grottesi, Chen and Pan https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Hong, Wandong Zhou, Xiaoying Jin, Shengchun Lu, Yajing Pan, Jingyi Lin, Qingyi Yang, Shaopeng Xu, Tingting Basharat, Zarrin Zippi, Maddalena Fiorino, Sirio Tsukanov, Vladislav Stock, Simon Grottesi, Alfonso Chen, Qin Pan, Jingye A Comparison of XGBoost, Random Forest, and Nomograph for the Prediction of Disease Severity in Patients With COVID-19 Pneumonia: Implications of Cytokine and Immune Cell Profile |
title | A Comparison of XGBoost, Random Forest, and Nomograph for the Prediction of Disease Severity in Patients With COVID-19 Pneumonia: Implications of Cytokine and Immune Cell Profile |
title_full | A Comparison of XGBoost, Random Forest, and Nomograph for the Prediction of Disease Severity in Patients With COVID-19 Pneumonia: Implications of Cytokine and Immune Cell Profile |
title_fullStr | A Comparison of XGBoost, Random Forest, and Nomograph for the Prediction of Disease Severity in Patients With COVID-19 Pneumonia: Implications of Cytokine and Immune Cell Profile |
title_full_unstemmed | A Comparison of XGBoost, Random Forest, and Nomograph for the Prediction of Disease Severity in Patients With COVID-19 Pneumonia: Implications of Cytokine and Immune Cell Profile |
title_short | A Comparison of XGBoost, Random Forest, and Nomograph for the Prediction of Disease Severity in Patients With COVID-19 Pneumonia: Implications of Cytokine and Immune Cell Profile |
title_sort | comparison of xgboost, random forest, and nomograph for the prediction of disease severity in patients with covid-19 pneumonia: implications of cytokine and immune cell profile |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039730/ https://www.ncbi.nlm.nih.gov/pubmed/35493729 http://dx.doi.org/10.3389/fcimb.2022.819267 |
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