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Neutrophil gelatinase associated lipocalin a biomarker for bacterial‐induced pharyngeal infection—A pilot study

OBJECTIVES: Neutrophil gelatinase associated lipocalin (NGAL) is secreted from activated neutrophil granulocytes and is considered an acute phase protein. The aim of this pilot study was to determine whether the NGAL concentration in saliva increases in response to a bacterial throat infection and i...

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Autores principales: Walvik, Lena, Kirchmann, Malene, Jensen, Claus Antonio Juel, Kristiansen, Søren, Hansen, Lennart Friis, Howitz, Michael Frantz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453767/
https://www.ncbi.nlm.nih.gov/pubmed/32337861
http://dx.doi.org/10.1002/cre2.295
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author Walvik, Lena
Kirchmann, Malene
Jensen, Claus Antonio Juel
Kristiansen, Søren
Hansen, Lennart Friis
Howitz, Michael Frantz
author_facet Walvik, Lena
Kirchmann, Malene
Jensen, Claus Antonio Juel
Kristiansen, Søren
Hansen, Lennart Friis
Howitz, Michael Frantz
author_sort Walvik, Lena
collection PubMed
description OBJECTIVES: Neutrophil gelatinase associated lipocalin (NGAL) is secreted from activated neutrophil granulocytes and is considered an acute phase protein. The aim of this pilot study was to determine whether the NGAL concentration in saliva increases in response to a bacterial throat infection and identify pitfalls, which shall be taken into account in a protocol in a larger hypothesis testing study. METHODS: Saliva samples for measurement of NGAL concentration where obtained from cases with an acute throat infection (n = 21) and controls (n = 24). Among cases, plasma NGAL, plasma CRP, and whole blood leukocytes, were measured as well. RESULTS: There was no significant difference in NGAL saliva concentration between cases and controls overall (p = .31). For both cases and controls, the saliva NGAL concentration decreased significantly after cleansing the mouth with tap water (cases p = .01; controls p = .01). Among cases, a significant positive correlation between saliva NGAL concentrations before mouth cleansing and plasma CRP concentrations (p = .001) was observed. Blood neutrophil granulocyte count presented a nonsignificant positive correlation to saliva NGAL (p = .07). CONCLUSION: We could not demonstrate a simple association between the salivary NGAL concentration and pharyngeal bacterial infection. Furthermore, the salivary NGAL concentrations were higher among some controls than cases, suggesting that cofounders for example, periodontitis, uneven salivary dilution level, or other exogenous factors affect salivary NGAL content.
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spelling pubmed-74537672020-09-02 Neutrophil gelatinase associated lipocalin a biomarker for bacterial‐induced pharyngeal infection—A pilot study Walvik, Lena Kirchmann, Malene Jensen, Claus Antonio Juel Kristiansen, Søren Hansen, Lennart Friis Howitz, Michael Frantz Clin Exp Dent Res Original Articles OBJECTIVES: Neutrophil gelatinase associated lipocalin (NGAL) is secreted from activated neutrophil granulocytes and is considered an acute phase protein. The aim of this pilot study was to determine whether the NGAL concentration in saliva increases in response to a bacterial throat infection and identify pitfalls, which shall be taken into account in a protocol in a larger hypothesis testing study. METHODS: Saliva samples for measurement of NGAL concentration where obtained from cases with an acute throat infection (n = 21) and controls (n = 24). Among cases, plasma NGAL, plasma CRP, and whole blood leukocytes, were measured as well. RESULTS: There was no significant difference in NGAL saliva concentration between cases and controls overall (p = .31). For both cases and controls, the saliva NGAL concentration decreased significantly after cleansing the mouth with tap water (cases p = .01; controls p = .01). Among cases, a significant positive correlation between saliva NGAL concentrations before mouth cleansing and plasma CRP concentrations (p = .001) was observed. Blood neutrophil granulocyte count presented a nonsignificant positive correlation to saliva NGAL (p = .07). CONCLUSION: We could not demonstrate a simple association between the salivary NGAL concentration and pharyngeal bacterial infection. Furthermore, the salivary NGAL concentrations were higher among some controls than cases, suggesting that cofounders for example, periodontitis, uneven salivary dilution level, or other exogenous factors affect salivary NGAL content. John Wiley and Sons Inc. 2020-04-26 /pmc/articles/PMC7453767/ /pubmed/32337861 http://dx.doi.org/10.1002/cre2.295 Text en © 2020 The Authors. Clinical and Experimental Dental Research published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Walvik, Lena
Kirchmann, Malene
Jensen, Claus Antonio Juel
Kristiansen, Søren
Hansen, Lennart Friis
Howitz, Michael Frantz
Neutrophil gelatinase associated lipocalin a biomarker for bacterial‐induced pharyngeal infection—A pilot study
title Neutrophil gelatinase associated lipocalin a biomarker for bacterial‐induced pharyngeal infection—A pilot study
title_full Neutrophil gelatinase associated lipocalin a biomarker for bacterial‐induced pharyngeal infection—A pilot study
title_fullStr Neutrophil gelatinase associated lipocalin a biomarker for bacterial‐induced pharyngeal infection—A pilot study
title_full_unstemmed Neutrophil gelatinase associated lipocalin a biomarker for bacterial‐induced pharyngeal infection—A pilot study
title_short Neutrophil gelatinase associated lipocalin a biomarker for bacterial‐induced pharyngeal infection—A pilot study
title_sort neutrophil gelatinase associated lipocalin a biomarker for bacterial‐induced pharyngeal infection—a pilot study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453767/
https://www.ncbi.nlm.nih.gov/pubmed/32337861
http://dx.doi.org/10.1002/cre2.295
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