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Active regression model for clinical grading of COVID-19

BACKGROUND: In the therapeutic process of COVID-19, the majority of indicators that physicians have for assisting treatment have come from clinical tests represented by proteins, metabolites, and immune levels in patients’ blood. Therefore, this study constructs an individualized treatment model bas...

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Autores principales: Sh, Yuan, Dong, Jierong, Chen, Zhongqing, Yuan, Meiqing, Lyu, Lingna, Zhang, Xiuli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071017/
https://www.ncbi.nlm.nih.gov/pubmed/37026015
http://dx.doi.org/10.3389/fimmu.2023.1141996
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author Sh, Yuan
Dong, Jierong
Chen, Zhongqing
Yuan, Meiqing
Lyu, Lingna
Zhang, Xiuli
author_facet Sh, Yuan
Dong, Jierong
Chen, Zhongqing
Yuan, Meiqing
Lyu, Lingna
Zhang, Xiuli
author_sort Sh, Yuan
collection PubMed
description BACKGROUND: In the therapeutic process of COVID-19, the majority of indicators that physicians have for assisting treatment have come from clinical tests represented by proteins, metabolites, and immune levels in patients’ blood. Therefore, this study constructs an individualized treatment model based on deep learning methods, aiming to realize timely intervention based on clinical test indicator data of COVID-19 patients and provide an important theoretical basis for optimizing medical resource allocation. METHODS: This study collected clinical data from a total of 1,799 individuals, including 560 controls for non-respiratory infectious diseases (Negative), 681 controls for other respiratory virus infections (Other), and 558 coronavirus infections (Positive) for COVID-19. We first used the Student T-test to screen for statistically significant differences (Pvalue<0.05); we then used the Adaptive-Lasso method stepwise regression to screen the characteristic variables and filter the features with low importance; we then used analysis of covariance to calculate the correlation between variables and filter the highly correlated features; and finally, we analyzed the feature contribution and screened the best combination of features. RESULTS: Feature engineering reduced the feature set to 13 feature combinations. The correlation coefficient between the projected results of the artificial intelligence-based individualized diagnostic model and the fitted curve of the actual values in the test group was 0.9449 which could be applied to the clinical prognosis of COVID-19. In addition, the depletion of platelets in patients with COVID-19 is an important factor affecting their severe deterioration. With the progression of COVID-19, there is a slight decrease in the total number of platelets in the patient’s body, particularly as the volume of larger platelets sharply decreases. The importance of plateletCV (count*mean platelet volume) in evaluating the severity of COVID-19 patients is higher than the count of platelets and mean platelet volume. CONCLUSION: In general, we found that for patients with COVID-19, the increase in mean platelet volume was a predictor for SARS-Cov-2. The rapid decrease of platelet volume and the decrease of total platelet volume are dangerous signals for the aggravation of SARS-Cov-2 infection. The analysis and modeling results of this study provide a new perspective for individualized accurate diagnosis and treatment of clinical COVID-19 patients.
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spelling pubmed-100710172023-04-05 Active regression model for clinical grading of COVID-19 Sh, Yuan Dong, Jierong Chen, Zhongqing Yuan, Meiqing Lyu, Lingna Zhang, Xiuli Front Immunol Immunology BACKGROUND: In the therapeutic process of COVID-19, the majority of indicators that physicians have for assisting treatment have come from clinical tests represented by proteins, metabolites, and immune levels in patients’ blood. Therefore, this study constructs an individualized treatment model based on deep learning methods, aiming to realize timely intervention based on clinical test indicator data of COVID-19 patients and provide an important theoretical basis for optimizing medical resource allocation. METHODS: This study collected clinical data from a total of 1,799 individuals, including 560 controls for non-respiratory infectious diseases (Negative), 681 controls for other respiratory virus infections (Other), and 558 coronavirus infections (Positive) for COVID-19. We first used the Student T-test to screen for statistically significant differences (Pvalue<0.05); we then used the Adaptive-Lasso method stepwise regression to screen the characteristic variables and filter the features with low importance; we then used analysis of covariance to calculate the correlation between variables and filter the highly correlated features; and finally, we analyzed the feature contribution and screened the best combination of features. RESULTS: Feature engineering reduced the feature set to 13 feature combinations. The correlation coefficient between the projected results of the artificial intelligence-based individualized diagnostic model and the fitted curve of the actual values in the test group was 0.9449 which could be applied to the clinical prognosis of COVID-19. In addition, the depletion of platelets in patients with COVID-19 is an important factor affecting their severe deterioration. With the progression of COVID-19, there is a slight decrease in the total number of platelets in the patient’s body, particularly as the volume of larger platelets sharply decreases. The importance of plateletCV (count*mean platelet volume) in evaluating the severity of COVID-19 patients is higher than the count of platelets and mean platelet volume. CONCLUSION: In general, we found that for patients with COVID-19, the increase in mean platelet volume was a predictor for SARS-Cov-2. The rapid decrease of platelet volume and the decrease of total platelet volume are dangerous signals for the aggravation of SARS-Cov-2 infection. The analysis and modeling results of this study provide a new perspective for individualized accurate diagnosis and treatment of clinical COVID-19 patients. Frontiers Media S.A. 2023-03-21 /pmc/articles/PMC10071017/ /pubmed/37026015 http://dx.doi.org/10.3389/fimmu.2023.1141996 Text en Copyright © 2023 Sh, Dong, Chen, Yuan, Lyu and Zhang 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 Immunology
Sh, Yuan
Dong, Jierong
Chen, Zhongqing
Yuan, Meiqing
Lyu, Lingna
Zhang, Xiuli
Active regression model for clinical grading of COVID-19
title Active regression model for clinical grading of COVID-19
title_full Active regression model for clinical grading of COVID-19
title_fullStr Active regression model for clinical grading of COVID-19
title_full_unstemmed Active regression model for clinical grading of COVID-19
title_short Active regression model for clinical grading of COVID-19
title_sort active regression model for clinical grading of covid-19
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071017/
https://www.ncbi.nlm.nih.gov/pubmed/37026015
http://dx.doi.org/10.3389/fimmu.2023.1141996
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