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Long Noncoding RNA and Predictive Model To Improve Diagnosis of Clinically Diagnosed Pulmonary Tuberculosis

Clinically diagnosed pulmonary tuberculosis (PTB) patients lack microbiological evidence of Mycobacterium tuberculosis, and misdiagnosis or delayed diagnosis often occurs as a consequence. We investigated the potential of long noncoding RNAs (lncRNAs) and corresponding predictive models to diagnose...

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Autores principales: Hu, Xuejiao, Liao, Shun, Bai, Hao, Gupta, Shubham, Zhou, Yi, Zhou, Juan, Jiao, Lin, Wu, Lijuan, Wang, Minjin, Chen, Xuerong, Zhou, Yanhong, Lu, Xiaojun, Hu, Tony Y., Zhang, Zhaolei, Ying, Binwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315016/
https://www.ncbi.nlm.nih.gov/pubmed/32295893
http://dx.doi.org/10.1128/JCM.01973-19
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author Hu, Xuejiao
Liao, Shun
Bai, Hao
Gupta, Shubham
Zhou, Yi
Zhou, Juan
Jiao, Lin
Wu, Lijuan
Wang, Minjin
Chen, Xuerong
Zhou, Yanhong
Lu, Xiaojun
Hu, Tony Y.
Zhang, Zhaolei
Ying, Binwu
author_facet Hu, Xuejiao
Liao, Shun
Bai, Hao
Gupta, Shubham
Zhou, Yi
Zhou, Juan
Jiao, Lin
Wu, Lijuan
Wang, Minjin
Chen, Xuerong
Zhou, Yanhong
Lu, Xiaojun
Hu, Tony Y.
Zhang, Zhaolei
Ying, Binwu
author_sort Hu, Xuejiao
collection PubMed
description Clinically diagnosed pulmonary tuberculosis (PTB) patients lack microbiological evidence of Mycobacterium tuberculosis, and misdiagnosis or delayed diagnosis often occurs as a consequence. We investigated the potential of long noncoding RNAs (lncRNAs) and corresponding predictive models to diagnose these patients. We enrolled 1,764 subjects, including clinically diagnosed PTB patients, microbiologically confirmed PTB cases, non-TB disease controls, and healthy controls, in three cohorts (screening, selection, and validation). Candidate lncRNAs differentially expressed in blood samples of the PTB and healthy control groups were identified by microarray and reverse transcription-quantitative PCR (qRT-PCR) in the screening cohort. Logistic regression models were developed using lncRNAs and/or electronic health records (EHRs) from clinically diagnosed PTB patients and non-TB disease controls in the selection cohort. These models were evaluated by area under the concentration-time curve (AUC) and decision curve analyses, and the optimal model was presented as a Web-based nomogram, which was evaluated in the validation cohort. Three differentially expressed lncRNAs (ENST00000497872, n333737, and n335265) were identified. The optimal model (i.e., nomogram) incorporated these three lncRNAs and six EHRs (age, hemoglobin, weight loss, low-grade fever, calcification detected by computed tomography [CT calcification], and interferon gamma release assay for tuberculosis [TB-IGRA]). The nomogram showed an AUC of 0.89, a sensitivity of 0.86, and a specificity of 0.82 in differentiating clinically diagnosed PTB cases from non-TB disease controls of the validation cohort, which demonstrated better discrimination and clinical net benefit than the EHR model. The nomogram also had a discriminative power (AUC, 0.90; sensitivity, 0.85; specificity, 0.81) in identifying microbiologically confirmed PTB patients. lncRNAs and the user-friendly nomogram could facilitate the early identification of PTB cases among suspected patients with negative M. tuberculosis microbiological evidence.
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spelling pubmed-73150162020-07-10 Long Noncoding RNA and Predictive Model To Improve Diagnosis of Clinically Diagnosed Pulmonary Tuberculosis Hu, Xuejiao Liao, Shun Bai, Hao Gupta, Shubham Zhou, Yi Zhou, Juan Jiao, Lin Wu, Lijuan Wang, Minjin Chen, Xuerong Zhou, Yanhong Lu, Xiaojun Hu, Tony Y. Zhang, Zhaolei Ying, Binwu J Clin Microbiol Mycobacteriology and Aerobic Actinomycetes Clinically diagnosed pulmonary tuberculosis (PTB) patients lack microbiological evidence of Mycobacterium tuberculosis, and misdiagnosis or delayed diagnosis often occurs as a consequence. We investigated the potential of long noncoding RNAs (lncRNAs) and corresponding predictive models to diagnose these patients. We enrolled 1,764 subjects, including clinically diagnosed PTB patients, microbiologically confirmed PTB cases, non-TB disease controls, and healthy controls, in three cohorts (screening, selection, and validation). Candidate lncRNAs differentially expressed in blood samples of the PTB and healthy control groups were identified by microarray and reverse transcription-quantitative PCR (qRT-PCR) in the screening cohort. Logistic regression models were developed using lncRNAs and/or electronic health records (EHRs) from clinically diagnosed PTB patients and non-TB disease controls in the selection cohort. These models were evaluated by area under the concentration-time curve (AUC) and decision curve analyses, and the optimal model was presented as a Web-based nomogram, which was evaluated in the validation cohort. Three differentially expressed lncRNAs (ENST00000497872, n333737, and n335265) were identified. The optimal model (i.e., nomogram) incorporated these three lncRNAs and six EHRs (age, hemoglobin, weight loss, low-grade fever, calcification detected by computed tomography [CT calcification], and interferon gamma release assay for tuberculosis [TB-IGRA]). The nomogram showed an AUC of 0.89, a sensitivity of 0.86, and a specificity of 0.82 in differentiating clinically diagnosed PTB cases from non-TB disease controls of the validation cohort, which demonstrated better discrimination and clinical net benefit than the EHR model. The nomogram also had a discriminative power (AUC, 0.90; sensitivity, 0.85; specificity, 0.81) in identifying microbiologically confirmed PTB patients. lncRNAs and the user-friendly nomogram could facilitate the early identification of PTB cases among suspected patients with negative M. tuberculosis microbiological evidence. American Society for Microbiology 2020-06-24 /pmc/articles/PMC7315016/ /pubmed/32295893 http://dx.doi.org/10.1128/JCM.01973-19 Text en Copyright © 2020 Hu et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Mycobacteriology and Aerobic Actinomycetes
Hu, Xuejiao
Liao, Shun
Bai, Hao
Gupta, Shubham
Zhou, Yi
Zhou, Juan
Jiao, Lin
Wu, Lijuan
Wang, Minjin
Chen, Xuerong
Zhou, Yanhong
Lu, Xiaojun
Hu, Tony Y.
Zhang, Zhaolei
Ying, Binwu
Long Noncoding RNA and Predictive Model To Improve Diagnosis of Clinically Diagnosed Pulmonary Tuberculosis
title Long Noncoding RNA and Predictive Model To Improve Diagnosis of Clinically Diagnosed Pulmonary Tuberculosis
title_full Long Noncoding RNA and Predictive Model To Improve Diagnosis of Clinically Diagnosed Pulmonary Tuberculosis
title_fullStr Long Noncoding RNA and Predictive Model To Improve Diagnosis of Clinically Diagnosed Pulmonary Tuberculosis
title_full_unstemmed Long Noncoding RNA and Predictive Model To Improve Diagnosis of Clinically Diagnosed Pulmonary Tuberculosis
title_short Long Noncoding RNA and Predictive Model To Improve Diagnosis of Clinically Diagnosed Pulmonary Tuberculosis
title_sort long noncoding rna and predictive model to improve diagnosis of clinically diagnosed pulmonary tuberculosis
topic Mycobacteriology and Aerobic Actinomycetes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315016/
https://www.ncbi.nlm.nih.gov/pubmed/32295893
http://dx.doi.org/10.1128/JCM.01973-19
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