Clara Cell Protein (Club Cell Protein) is a New Diagnostic Molecular Candidate Biomarker in Nosocomial Pneumonia

Nosocomial pneumonia (NP) remains a relevant problem of resuscitation. Molecular biomarkers are significant promises for diagnosing NP. Objective: to estimate the informative value of the plasma levels of Clara cell protein (Club Cell Protein, CCP) as a diagnostic molecular candidate biomarker in NP...

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Main Authors: V. V. Moroz, A. M. Golubev, A. N. Kuzovlev, A. K. Shabanov, V. M. Pisarev
Format: Article
Language:Russian
Published: Russian Academy of Medical Sciences 2014-12-01
Series:Obŝaâ Reanimatologiâ
Subjects:
Online Access:https://www.reanimatology.com/rmt/article/view/1427
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spelling doaj-e64cb0f95d704a5a8695fc1279bc3e102021-07-28T21:21:54ZrusRussian Academy of Medical SciencesObŝaâ Reanimatologiâ1813-97792411-71102014-12-0110661410.15360/1813-9779-2014-6-6-141424Clara Cell Protein (Club Cell Protein) is a New Diagnostic Molecular Candidate Biomarker in Nosocomial PneumoniaV. V. Moroz0A. M. Golubev1A. N. Kuzovlev2A. K. Shabanov3V. M. Pisarev4НИИ общей реаниматологии им. В. А. Неговского, Москва, Россия 107031, Москва, ул. Петровка, д. 25, стр. 2НИИ общей реаниматологии им. В. А. Неговского, Москва, Россия 107031, Москва, ул. Петровка, д. 25, стр. 2НИИ общей реаниматологии им. В. А. Неговского, Москва, Россия 107031, Москва, ул. Петровка, д. 25, стр. 2НИИ скорой помощи им. Н. В. Склифосовского, Москва, Россия 129010, Москва, Б. Сухаревская пл., д. 3НИИ общей реаниматологии им. В. А. Неговского, Москва, Россия 107031, Москва, ул. Петровка, д. 25, стр. 2Nosocomial pneumonia (NP) remains a relevant problem of resuscitation. Molecular biomarkers are significant promises for diagnosing NP. Objective: to estimate the informative value of the plasma levels of Clara cell protein (Club Cell Protein, CCP) as a diagnostic molecular candidate biomarker in NP. Subjects and methods. The investigation was conducted at the Research Institute of General Reanimatology (RIGR), Russian Academy of Medical Sciences (RAMS), in 2010—2013. It included 85 patients in accordance with the criteria of inclusion and exclusion and 30 donors. Acute respiratory distress syndrome and its stages were diagnosed using the criteria of RIGR, RAMS. Plasma Clara cell protein (CCP) levels were measured by the enzyme immunoassay Human Clara Cell Protein ELISA, RD191022200, BioVendor, USA. The findings were statistically analyzed using the package Statistica 7.0. ROC curve analysis was made to determine the sensitivity andspecificity of CCP. The difference at p<0.05 was considered significant. Results. On days 1, 3, 5, and 7 of the investigation, the plasma CCP levels in patients with NP were lower than in those without this disease. Within all these days, the plasma CCP concentrations in patients with and without NP were higher than in healthy donors. On days 1 and 3, the plasma content of CCP was much lower in patients in whom NP had been caused by Pseudomonas aeruginosa (in association with other pathogens) than in those with NP uncaused by Pseudomonas aeruginosa. Within the first 24 hours, the CCP level of 17.5 ng/ml had 86.5% sensitivity and 66.7% specificity in diagnosing Pseudomonas aeruginosainduced NP (area undercurve, 0.74; 95% confidence interval, 0.630—0.829; p=0.0001). The prognostic value of the positive and negative results of this test was 81.8 and 74.1%, respectively. Conclusion. The time course of changes in the plasma levels of Clara cell protein was studied in the patients with nosocomial pneumonia. Clara cell protein was shown to be of informative value in the diag nosis of Pseudomonas aeruginosainduced NP; on the day when nosocomial pneumonia was diagnosed, the plasma CCP level of 17.5 ng/ml had 86.5% sensitivity and 66.7% specificity in diagnosing Pseudomonas aeruginosainduced NP.https://www.reanimatology.com/rmt/article/view/1427nosocomial pneumoniabiomarkerclara cell proteindiagnosissepsis.
collection DOAJ
language Russian
format Article
sources DOAJ
author V. V. Moroz
A. M. Golubev
A. N. Kuzovlev
A. K. Shabanov
V. M. Pisarev
spellingShingle V. V. Moroz
A. M. Golubev
A. N. Kuzovlev
A. K. Shabanov
V. M. Pisarev
Clara Cell Protein (Club Cell Protein) is a New Diagnostic Molecular Candidate Biomarker in Nosocomial Pneumonia
Obŝaâ Reanimatologiâ
nosocomial pneumonia
biomarker
clara cell protein
diagnosis
sepsis.
author_facet V. V. Moroz
A. M. Golubev
A. N. Kuzovlev
A. K. Shabanov
V. M. Pisarev
author_sort V. V. Moroz
title Clara Cell Protein (Club Cell Protein) is a New Diagnostic Molecular Candidate Biomarker in Nosocomial Pneumonia
title_short Clara Cell Protein (Club Cell Protein) is a New Diagnostic Molecular Candidate Biomarker in Nosocomial Pneumonia
title_full Clara Cell Protein (Club Cell Protein) is a New Diagnostic Molecular Candidate Biomarker in Nosocomial Pneumonia
title_fullStr Clara Cell Protein (Club Cell Protein) is a New Diagnostic Molecular Candidate Biomarker in Nosocomial Pneumonia
title_full_unstemmed Clara Cell Protein (Club Cell Protein) is a New Diagnostic Molecular Candidate Biomarker in Nosocomial Pneumonia
title_sort clara cell protein (club cell protein) is a new diagnostic molecular candidate biomarker in nosocomial pneumonia
publisher Russian Academy of Medical Sciences
series Obŝaâ Reanimatologiâ
issn 1813-9779
2411-7110
publishDate 2014-12-01
description Nosocomial pneumonia (NP) remains a relevant problem of resuscitation. Molecular biomarkers are significant promises for diagnosing NP. Objective: to estimate the informative value of the plasma levels of Clara cell protein (Club Cell Protein, CCP) as a diagnostic molecular candidate biomarker in NP. Subjects and methods. The investigation was conducted at the Research Institute of General Reanimatology (RIGR), Russian Academy of Medical Sciences (RAMS), in 2010—2013. It included 85 patients in accordance with the criteria of inclusion and exclusion and 30 donors. Acute respiratory distress syndrome and its stages were diagnosed using the criteria of RIGR, RAMS. Plasma Clara cell protein (CCP) levels were measured by the enzyme immunoassay Human Clara Cell Protein ELISA, RD191022200, BioVendor, USA. The findings were statistically analyzed using the package Statistica 7.0. ROC curve analysis was made to determine the sensitivity andspecificity of CCP. The difference at p<0.05 was considered significant. Results. On days 1, 3, 5, and 7 of the investigation, the plasma CCP levels in patients with NP were lower than in those without this disease. Within all these days, the plasma CCP concentrations in patients with and without NP were higher than in healthy donors. On days 1 and 3, the plasma content of CCP was much lower in patients in whom NP had been caused by Pseudomonas aeruginosa (in association with other pathogens) than in those with NP uncaused by Pseudomonas aeruginosa. Within the first 24 hours, the CCP level of 17.5 ng/ml had 86.5% sensitivity and 66.7% specificity in diagnosing Pseudomonas aeruginosainduced NP (area undercurve, 0.74; 95% confidence interval, 0.630—0.829; p=0.0001). The prognostic value of the positive and negative results of this test was 81.8 and 74.1%, respectively. Conclusion. The time course of changes in the plasma levels of Clara cell protein was studied in the patients with nosocomial pneumonia. Clara cell protein was shown to be of informative value in the diag nosis of Pseudomonas aeruginosainduced NP; on the day when nosocomial pneumonia was diagnosed, the plasma CCP level of 17.5 ng/ml had 86.5% sensitivity and 66.7% specificity in diagnosing Pseudomonas aeruginosainduced NP.
topic nosocomial pneumonia
biomarker
clara cell protein
diagnosis
sepsis.
url https://www.reanimatology.com/rmt/article/view/1427
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