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Significance of fractional exhaled nitric oxide in chronic eosinophilic pneumonia: a retrospective cohort study
BACKGROUND: Chronic eosinophilic pneumonia (CEP) is characterized by chronic eosinophilic infiltration of the lung. It is dramatically responsive to corticosteroid treatment, but symptoms and radiopacities recur frequently after tapering or discontinuing the medication. Fractional exhaled nitric oxi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4024211/ https://www.ncbi.nlm.nih.gov/pubmed/24885379 http://dx.doi.org/10.1186/1471-2466-14-81 |
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author | Park, Ji Young Lee, Taehoon Lee, Hongyeul Lee, Yeon Joo Park, Jong Sun Cho, Young-Jae Yoon, Ho Il Lee, Jae Ho Lee, Choon-Taek |
author_facet | Park, Ji Young Lee, Taehoon Lee, Hongyeul Lee, Yeon Joo Park, Jong Sun Cho, Young-Jae Yoon, Ho Il Lee, Jae Ho Lee, Choon-Taek |
author_sort | Park, Ji Young |
collection | PubMed |
description | BACKGROUND: Chronic eosinophilic pneumonia (CEP) is characterized by chronic eosinophilic infiltration of the lung. It is dramatically responsive to corticosteroid treatment, but symptoms and radiopacities recur frequently after tapering or discontinuing the medication. Fractional exhaled nitric oxide (FeNO) is a well-known noninvasive marker of eosinophilic airway inflammation. The aim of this retrospective cohort study was to investigate the relationships of FeNO with peripheral eosinophilia and the clinical state of CEP and its validity for predicting exacerbation of CEP. METHODS: Standard clinical and laboratory parameters, peripheral eosinophil percentage and count, and FeNO level were measured in 18 patients with CEP at several assessment points over 1 year. RESULTS: FeNO level was positively correlated with peripheral eosinophil count (r = 0.341, P = 0.005) and percentage (r = 0.362, P = 0.003). The median (IQR) FeNO levels were 79 (41–88) and 35 (26–49) ppb in uncontrolled (13/74 measurements) and controlled (61/74 measurements) CEP, respectively (P = 0.010). The FeNO level of 66.0 ppb showed the largest area under the curve (0.835) for predicting exacerbation of CEP (sensitivity = 0.80, specificity = 0.84). CONCLUSION: FeNO may be useful for monitoring eosinophilic parenchymal inflammation and determining the appropriate corticosteroid dose in CEP. |
format | Online Article Text |
id | pubmed-4024211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40242112014-05-18 Significance of fractional exhaled nitric oxide in chronic eosinophilic pneumonia: a retrospective cohort study Park, Ji Young Lee, Taehoon Lee, Hongyeul Lee, Yeon Joo Park, Jong Sun Cho, Young-Jae Yoon, Ho Il Lee, Jae Ho Lee, Choon-Taek BMC Pulm Med Research Article BACKGROUND: Chronic eosinophilic pneumonia (CEP) is characterized by chronic eosinophilic infiltration of the lung. It is dramatically responsive to corticosteroid treatment, but symptoms and radiopacities recur frequently after tapering or discontinuing the medication. Fractional exhaled nitric oxide (FeNO) is a well-known noninvasive marker of eosinophilic airway inflammation. The aim of this retrospective cohort study was to investigate the relationships of FeNO with peripheral eosinophilia and the clinical state of CEP and its validity for predicting exacerbation of CEP. METHODS: Standard clinical and laboratory parameters, peripheral eosinophil percentage and count, and FeNO level were measured in 18 patients with CEP at several assessment points over 1 year. RESULTS: FeNO level was positively correlated with peripheral eosinophil count (r = 0.341, P = 0.005) and percentage (r = 0.362, P = 0.003). The median (IQR) FeNO levels were 79 (41–88) and 35 (26–49) ppb in uncontrolled (13/74 measurements) and controlled (61/74 measurements) CEP, respectively (P = 0.010). The FeNO level of 66.0 ppb showed the largest area under the curve (0.835) for predicting exacerbation of CEP (sensitivity = 0.80, specificity = 0.84). CONCLUSION: FeNO may be useful for monitoring eosinophilic parenchymal inflammation and determining the appropriate corticosteroid dose in CEP. BioMed Central 2014-05-12 /pmc/articles/PMC4024211/ /pubmed/24885379 http://dx.doi.org/10.1186/1471-2466-14-81 Text en Copyright © 2014 Park et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Park, Ji Young Lee, Taehoon Lee, Hongyeul Lee, Yeon Joo Park, Jong Sun Cho, Young-Jae Yoon, Ho Il Lee, Jae Ho Lee, Choon-Taek Significance of fractional exhaled nitric oxide in chronic eosinophilic pneumonia: a retrospective cohort study |
title | Significance of fractional exhaled nitric oxide in chronic eosinophilic pneumonia: a retrospective cohort study |
title_full | Significance of fractional exhaled nitric oxide in chronic eosinophilic pneumonia: a retrospective cohort study |
title_fullStr | Significance of fractional exhaled nitric oxide in chronic eosinophilic pneumonia: a retrospective cohort study |
title_full_unstemmed | Significance of fractional exhaled nitric oxide in chronic eosinophilic pneumonia: a retrospective cohort study |
title_short | Significance of fractional exhaled nitric oxide in chronic eosinophilic pneumonia: a retrospective cohort study |
title_sort | significance of fractional exhaled nitric oxide in chronic eosinophilic pneumonia: a retrospective cohort study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4024211/ https://www.ncbi.nlm.nih.gov/pubmed/24885379 http://dx.doi.org/10.1186/1471-2466-14-81 |
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