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Altered serum microRNAs as biomarkers for the early diagnosis of pulmonary tuberculosis infection

BACKGROUND: Pulmonary tuberculosis (TB) is a highly lethal infectious disease and early diagnosis of TB is critical for the control of disease progression. The objective of this study was to profile a panel of serum microRNAs (miRNAs) as potential biomarkers for the early diagnosis of pulmonary TB i...

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Autores principales: Qi, Yuhua, Cui, Lunbiao, Ge, Yiyue, Shi, Zhiyang, Zhao, Kangchen, Guo, Xiling, Yang, Dandan, Yu, Hao, Cui, Lan, Shan, Yunfeng, Zhou, Minghao, Wang, Hua, Lu, Zuhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568404/
https://www.ncbi.nlm.nih.gov/pubmed/23272999
http://dx.doi.org/10.1186/1471-2334-12-384
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author Qi, Yuhua
Cui, Lunbiao
Ge, Yiyue
Shi, Zhiyang
Zhao, Kangchen
Guo, Xiling
Yang, Dandan
Yu, Hao
Cui, Lan
Shan, Yunfeng
Zhou, Minghao
Wang, Hua
Lu, Zuhong
author_facet Qi, Yuhua
Cui, Lunbiao
Ge, Yiyue
Shi, Zhiyang
Zhao, Kangchen
Guo, Xiling
Yang, Dandan
Yu, Hao
Cui, Lan
Shan, Yunfeng
Zhou, Minghao
Wang, Hua
Lu, Zuhong
author_sort Qi, Yuhua
collection PubMed
description BACKGROUND: Pulmonary tuberculosis (TB) is a highly lethal infectious disease and early diagnosis of TB is critical for the control of disease progression. The objective of this study was to profile a panel of serum microRNAs (miRNAs) as potential biomarkers for the early diagnosis of pulmonary TB infection. METHODS: Using TaqMan Low-Density Array (TLDA) analysis followed by quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) validation, expression levels of miRNAs in serum samples from 30 patients with active tuberculosis and 60 patients with Bordetella pertussis (BP), varicella-zoster virus (VZV) and enterovirus (EV) were analyzed. RESULTS: The Low-Density Array data showed that 97 miRNAs were differentially expressed in pulmonary TB patient sera compared with healthy controls (90 up-regulated and 7 down-regulated). Following qRT-PCR confirmation and receiver operational curve (ROC) analysis, three miRNAs (miR-361-5p, miR-889 and miR-576-3p) were shown to distinguish TB infected patients from healthy controls and other microbial infections with moderate sensitivity and specificity (area under curve (AUC) value range, 0.711-0.848). Multiple logistic regression analysis of a combination of these three miRNAs showed an enhanced ability to discriminate between these two groups with an AUC value of 0.863. CONCLUSIONS: Our study suggests that altered levels of serum miRNAs have great potential to serve as non-invasive biomarkers for early detection of pulmonary TB infection.
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spelling pubmed-35684042013-02-11 Altered serum microRNAs as biomarkers for the early diagnosis of pulmonary tuberculosis infection Qi, Yuhua Cui, Lunbiao Ge, Yiyue Shi, Zhiyang Zhao, Kangchen Guo, Xiling Yang, Dandan Yu, Hao Cui, Lan Shan, Yunfeng Zhou, Minghao Wang, Hua Lu, Zuhong BMC Infect Dis Research Article BACKGROUND: Pulmonary tuberculosis (TB) is a highly lethal infectious disease and early diagnosis of TB is critical for the control of disease progression. The objective of this study was to profile a panel of serum microRNAs (miRNAs) as potential biomarkers for the early diagnosis of pulmonary TB infection. METHODS: Using TaqMan Low-Density Array (TLDA) analysis followed by quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) validation, expression levels of miRNAs in serum samples from 30 patients with active tuberculosis and 60 patients with Bordetella pertussis (BP), varicella-zoster virus (VZV) and enterovirus (EV) were analyzed. RESULTS: The Low-Density Array data showed that 97 miRNAs were differentially expressed in pulmonary TB patient sera compared with healthy controls (90 up-regulated and 7 down-regulated). Following qRT-PCR confirmation and receiver operational curve (ROC) analysis, three miRNAs (miR-361-5p, miR-889 and miR-576-3p) were shown to distinguish TB infected patients from healthy controls and other microbial infections with moderate sensitivity and specificity (area under curve (AUC) value range, 0.711-0.848). Multiple logistic regression analysis of a combination of these three miRNAs showed an enhanced ability to discriminate between these two groups with an AUC value of 0.863. CONCLUSIONS: Our study suggests that altered levels of serum miRNAs have great potential to serve as non-invasive biomarkers for early detection of pulmonary TB infection. BioMed Central 2012-12-28 /pmc/articles/PMC3568404/ /pubmed/23272999 http://dx.doi.org/10.1186/1471-2334-12-384 Text en Copyright ©2012 Qi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Qi, Yuhua
Cui, Lunbiao
Ge, Yiyue
Shi, Zhiyang
Zhao, Kangchen
Guo, Xiling
Yang, Dandan
Yu, Hao
Cui, Lan
Shan, Yunfeng
Zhou, Minghao
Wang, Hua
Lu, Zuhong
Altered serum microRNAs as biomarkers for the early diagnosis of pulmonary tuberculosis infection
title Altered serum microRNAs as biomarkers for the early diagnosis of pulmonary tuberculosis infection
title_full Altered serum microRNAs as biomarkers for the early diagnosis of pulmonary tuberculosis infection
title_fullStr Altered serum microRNAs as biomarkers for the early diagnosis of pulmonary tuberculosis infection
title_full_unstemmed Altered serum microRNAs as biomarkers for the early diagnosis of pulmonary tuberculosis infection
title_short Altered serum microRNAs as biomarkers for the early diagnosis of pulmonary tuberculosis infection
title_sort altered serum micrornas as biomarkers for the early diagnosis of pulmonary tuberculosis infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568404/
https://www.ncbi.nlm.nih.gov/pubmed/23272999
http://dx.doi.org/10.1186/1471-2334-12-384
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