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Nicotinamide phosphoribosyltransferase as a biomarker for the diagnosis of infectious pleural effusions

Nicotinamide phosphoribosyltransferase (NAMPT) has been reported to be involved in infectious diseases, but it is unknown whether it plays a role in infectious pleural effusions (IPEs). We observed the levels of NAMPT in pleural effusions of different etiologies and investigated the clinical value o...

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Autores principales: Huang, Jing, Guo, Lun, Kang, Hong-Wei, Lv, Dan, Lin, Wei, Li, Chao-Fen, Huang, Xue-Qin, Ding, Qun-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548599/
https://www.ncbi.nlm.nih.gov/pubmed/34702907
http://dx.doi.org/10.1038/s41598-021-00653-4
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author Huang, Jing
Guo, Lun
Kang, Hong-Wei
Lv, Dan
Lin, Wei
Li, Chao-Fen
Huang, Xue-Qin
Ding, Qun-Li
author_facet Huang, Jing
Guo, Lun
Kang, Hong-Wei
Lv, Dan
Lin, Wei
Li, Chao-Fen
Huang, Xue-Qin
Ding, Qun-Li
author_sort Huang, Jing
collection PubMed
description Nicotinamide phosphoribosyltransferase (NAMPT) has been reported to be involved in infectious diseases, but it is unknown whether it plays a role in infectious pleural effusions (IPEs). We observed the levels of NAMPT in pleural effusions of different etiologies and investigated the clinical value of NAMPT in the differential diagnosis of infectious pleural effusions. A total of 111 patients with pleural effusion were enrolled in the study, including 25 parapneumonic effusions (PPEs) (17 uncomplicated PPEs, 3 complicated PPEs, and 5 empyemas), 30 tuberculous pleural effusions (TPEs), 36 malignant pleural effusions (MPEs), and 20 transudative effusions. Pleural fluid NAMPT levels were highest in the patients with empyemas [575.4 (457.7, 649.3) ng/ml], followed by those with complicated PPEs [113.5 (103.5, 155.29) ng/ml], uncomplicated PPEs [24.9 (20.2, 46.7) ng/ml] and TPEs [88 (19.4, 182.6) ng/ml], and lower in patients with MPEs [11.5 (6.5, 18.4) ng/ml] and transudative effusions [4.3 (2.6, 5.1) ng/ml]. Pleural fluid NAMPT levels were significantly higher in PPEs (P < 0.001) or TPEs (P < 0.001) than in MPEs. Moreover, Pleural fluid NAMPT levels were positively correlated with the neutrophil percentage and lactate dehydrogenase (LDH) levels and inversely correlated with glucose levels in both PPEs and TPEs, indicating that NAMPT was implicated in the neutrophil-associated inflammatory response in infectious pleural effusion. Further, multivariate logistic regression analysis showed pleural fluid NAMPT was a significant predictor distinguishing PPEs from MPEs [odds ratio (OR) 1.180, 95% confidence interval (CI) 1.052–1.324, P = 0.005]. Receiver-operating characteristic (ROC) analysis demonstrated that NAMPT was a promising diagnostic factor for the diagnosis of infectious effusions, with the areas under the curve for pleural fluid NAMPT distinguishing PPEs from MPEs, TPEs from MPEs, and IPEs (PPEs and TPEs) from NIPEs were 0.92, 0.85, and 0.88, respectively. In conclusion, pleural fluid NAMPT could be used as a biomarker for the diagnosis of infectious pleural effusions.
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spelling pubmed-85485992021-10-28 Nicotinamide phosphoribosyltransferase as a biomarker for the diagnosis of infectious pleural effusions Huang, Jing Guo, Lun Kang, Hong-Wei Lv, Dan Lin, Wei Li, Chao-Fen Huang, Xue-Qin Ding, Qun-Li Sci Rep Article Nicotinamide phosphoribosyltransferase (NAMPT) has been reported to be involved in infectious diseases, but it is unknown whether it plays a role in infectious pleural effusions (IPEs). We observed the levels of NAMPT in pleural effusions of different etiologies and investigated the clinical value of NAMPT in the differential diagnosis of infectious pleural effusions. A total of 111 patients with pleural effusion were enrolled in the study, including 25 parapneumonic effusions (PPEs) (17 uncomplicated PPEs, 3 complicated PPEs, and 5 empyemas), 30 tuberculous pleural effusions (TPEs), 36 malignant pleural effusions (MPEs), and 20 transudative effusions. Pleural fluid NAMPT levels were highest in the patients with empyemas [575.4 (457.7, 649.3) ng/ml], followed by those with complicated PPEs [113.5 (103.5, 155.29) ng/ml], uncomplicated PPEs [24.9 (20.2, 46.7) ng/ml] and TPEs [88 (19.4, 182.6) ng/ml], and lower in patients with MPEs [11.5 (6.5, 18.4) ng/ml] and transudative effusions [4.3 (2.6, 5.1) ng/ml]. Pleural fluid NAMPT levels were significantly higher in PPEs (P < 0.001) or TPEs (P < 0.001) than in MPEs. Moreover, Pleural fluid NAMPT levels were positively correlated with the neutrophil percentage and lactate dehydrogenase (LDH) levels and inversely correlated with glucose levels in both PPEs and TPEs, indicating that NAMPT was implicated in the neutrophil-associated inflammatory response in infectious pleural effusion. Further, multivariate logistic regression analysis showed pleural fluid NAMPT was a significant predictor distinguishing PPEs from MPEs [odds ratio (OR) 1.180, 95% confidence interval (CI) 1.052–1.324, P = 0.005]. Receiver-operating characteristic (ROC) analysis demonstrated that NAMPT was a promising diagnostic factor for the diagnosis of infectious effusions, with the areas under the curve for pleural fluid NAMPT distinguishing PPEs from MPEs, TPEs from MPEs, and IPEs (PPEs and TPEs) from NIPEs were 0.92, 0.85, and 0.88, respectively. In conclusion, pleural fluid NAMPT could be used as a biomarker for the diagnosis of infectious pleural effusions. Nature Publishing Group UK 2021-10-26 /pmc/articles/PMC8548599/ /pubmed/34702907 http://dx.doi.org/10.1038/s41598-021-00653-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Huang, Jing
Guo, Lun
Kang, Hong-Wei
Lv, Dan
Lin, Wei
Li, Chao-Fen
Huang, Xue-Qin
Ding, Qun-Li
Nicotinamide phosphoribosyltransferase as a biomarker for the diagnosis of infectious pleural effusions
title Nicotinamide phosphoribosyltransferase as a biomarker for the diagnosis of infectious pleural effusions
title_full Nicotinamide phosphoribosyltransferase as a biomarker for the diagnosis of infectious pleural effusions
title_fullStr Nicotinamide phosphoribosyltransferase as a biomarker for the diagnosis of infectious pleural effusions
title_full_unstemmed Nicotinamide phosphoribosyltransferase as a biomarker for the diagnosis of infectious pleural effusions
title_short Nicotinamide phosphoribosyltransferase as a biomarker for the diagnosis of infectious pleural effusions
title_sort nicotinamide phosphoribosyltransferase as a biomarker for the diagnosis of infectious pleural effusions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548599/
https://www.ncbi.nlm.nih.gov/pubmed/34702907
http://dx.doi.org/10.1038/s41598-021-00653-4
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