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Construction of a risk model and deep learning network based on patients with active pulmonary tuberculosis and pulmonary inflammation

Most patients with active pulmonary tuberculosis (TB) are difficult to be differentiated from pneumonia (PN), especially those with acid-fast bacillus smear-negative (AFB(-)) and interferon-γ release assay-positive (IGRA(+)) results. Thus, the aim of the present study was to develop a risk model of...

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Autores principales: Xu, Dechang, Zeng, Jiang, Xie, Fangfang, Yang, Qianting, Huang, Kaisong, Xiao, Wei, Zou, Houwen, Zhang, Huihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079808/
https://www.ncbi.nlm.nih.gov/pubmed/37034573
http://dx.doi.org/10.3892/br.2023.1616
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author Xu, Dechang
Zeng, Jiang
Xie, Fangfang
Yang, Qianting
Huang, Kaisong
Xiao, Wei
Zou, Houwen
Zhang, Huihua
author_facet Xu, Dechang
Zeng, Jiang
Xie, Fangfang
Yang, Qianting
Huang, Kaisong
Xiao, Wei
Zou, Houwen
Zhang, Huihua
author_sort Xu, Dechang
collection PubMed
description Most patients with active pulmonary tuberculosis (TB) are difficult to be differentiated from pneumonia (PN), especially those with acid-fast bacillus smear-negative (AFB(-)) and interferon-γ release assay-positive (IGRA(+)) results. Thus, the aim of the present study was to develop a risk model of low-cost and rapid test for the diagnosis of AFB(-) IGRA(+) TB from PN. A total of 41 laboratory variables of 204 AFB(-) IGRA(+) TB and 156 PN participants were retrospectively analyzed. Candidate variables were identified by t-statistic test and univariate logistic model. The logistic regression analysis was used to construct the multivariate risk model and nomogram with internal and external validation. A total of 13 statistically differential variables were compared between AFB(-) IGRA(+) TB and PN by false discovery rate (FDR) and odds ratio (OR). By integrating five variables, including age, uric acid (UA), albumin (ALB), hemoglobin (Hb) and white blood cell counts (WBC), a multivariate risk model with a concordance index (C-index) of 0.7 (95% CI: 0.61, 0.8) was constructed. The nomogram showed that UA and Hb acted as protective factors with an OR <1, while age, WBC and ALB were risk factors for TB occurrence. Internal and external validation revealed that nomogram prediction was consistent with the actual observations. Collectively, it was revealed that an integration of five biomarkers (age, UA, ALB, Hb and WBC) may be used to quickly predict TB in AFB(-) IGRA(+) clinical samples from PN.
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spelling pubmed-100798082023-04-08 Construction of a risk model and deep learning network based on patients with active pulmonary tuberculosis and pulmonary inflammation Xu, Dechang Zeng, Jiang Xie, Fangfang Yang, Qianting Huang, Kaisong Xiao, Wei Zou, Houwen Zhang, Huihua Biomed Rep Articles Most patients with active pulmonary tuberculosis (TB) are difficult to be differentiated from pneumonia (PN), especially those with acid-fast bacillus smear-negative (AFB(-)) and interferon-γ release assay-positive (IGRA(+)) results. Thus, the aim of the present study was to develop a risk model of low-cost and rapid test for the diagnosis of AFB(-) IGRA(+) TB from PN. A total of 41 laboratory variables of 204 AFB(-) IGRA(+) TB and 156 PN participants were retrospectively analyzed. Candidate variables were identified by t-statistic test and univariate logistic model. The logistic regression analysis was used to construct the multivariate risk model and nomogram with internal and external validation. A total of 13 statistically differential variables were compared between AFB(-) IGRA(+) TB and PN by false discovery rate (FDR) and odds ratio (OR). By integrating five variables, including age, uric acid (UA), albumin (ALB), hemoglobin (Hb) and white blood cell counts (WBC), a multivariate risk model with a concordance index (C-index) of 0.7 (95% CI: 0.61, 0.8) was constructed. The nomogram showed that UA and Hb acted as protective factors with an OR <1, while age, WBC and ALB were risk factors for TB occurrence. Internal and external validation revealed that nomogram prediction was consistent with the actual observations. Collectively, it was revealed that an integration of five biomarkers (age, UA, ALB, Hb and WBC) may be used to quickly predict TB in AFB(-) IGRA(+) clinical samples from PN. D.A. Spandidos 2023-03-28 /pmc/articles/PMC10079808/ /pubmed/37034573 http://dx.doi.org/10.3892/br.2023.1616 Text en Copyright: © Xu et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Xu, Dechang
Zeng, Jiang
Xie, Fangfang
Yang, Qianting
Huang, Kaisong
Xiao, Wei
Zou, Houwen
Zhang, Huihua
Construction of a risk model and deep learning network based on patients with active pulmonary tuberculosis and pulmonary inflammation
title Construction of a risk model and deep learning network based on patients with active pulmonary tuberculosis and pulmonary inflammation
title_full Construction of a risk model and deep learning network based on patients with active pulmonary tuberculosis and pulmonary inflammation
title_fullStr Construction of a risk model and deep learning network based on patients with active pulmonary tuberculosis and pulmonary inflammation
title_full_unstemmed Construction of a risk model and deep learning network based on patients with active pulmonary tuberculosis and pulmonary inflammation
title_short Construction of a risk model and deep learning network based on patients with active pulmonary tuberculosis and pulmonary inflammation
title_sort construction of a risk model and deep learning network based on patients with active pulmonary tuberculosis and pulmonary inflammation
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079808/
https://www.ncbi.nlm.nih.gov/pubmed/37034573
http://dx.doi.org/10.3892/br.2023.1616
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