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Clinical Utility of Central and Peripheral Airway Nitric Oxide in Aging Patients with Stable and Acute Exacerbated Chronic Obstructive Pulmonary Disease

PURPOSE: Exhaled nitric oxide has been used as a marker of airway inflammation. The NO concentration in the central and peripheral airway/alveolar can be measured by a slow and fast exhalation flow rate to evaluate inflammation in different divisions within the respiratory tract. We hypothesized tha...

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Autores principales: Fan, Xiaodong, Zhao, Nian, Yu, Zhen, Yu, Haoda, Yin, Bo, Zou, Lifei, Zhao, Yinying, Qian, Xiufen, Sai, Xiaoyan, Qin, Chu, Fu, Congli, Hu, Caixia, Di, Tingting, Yang, Yue, Wu, Yan, Bian, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7914066/
https://www.ncbi.nlm.nih.gov/pubmed/33654424
http://dx.doi.org/10.2147/IJGM.S284688
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author Fan, Xiaodong
Zhao, Nian
Yu, Zhen
Yu, Haoda
Yin, Bo
Zou, Lifei
Zhao, Yinying
Qian, Xiufen
Sai, Xiaoyan
Qin, Chu
Fu, Congli
Hu, Caixia
Di, Tingting
Yang, Yue
Wu, Yan
Bian, Tao
author_facet Fan, Xiaodong
Zhao, Nian
Yu, Zhen
Yu, Haoda
Yin, Bo
Zou, Lifei
Zhao, Yinying
Qian, Xiufen
Sai, Xiaoyan
Qin, Chu
Fu, Congli
Hu, Caixia
Di, Tingting
Yang, Yue
Wu, Yan
Bian, Tao
author_sort Fan, Xiaodong
collection PubMed
description PURPOSE: Exhaled nitric oxide has been used as a marker of airway inflammation. The NO concentration in the central and peripheral airway/alveolar can be measured by a slow and fast exhalation flow rate to evaluate inflammation in different divisions within the respiratory tract. We hypothesized that FeNO(200) (exhaled NO at a flow rate of 200mL/s) could be used as an evaluation tool for peripheral airway/alveolar inflammation and corticosteroid therapy in chronic obstructive pulmonary disease (COPD) patients. METHODS: We recruited 171 subjects into the study: 73 healthy controls, 59 stable COPD patients, and 39 acute exacerbations of COPD (AECOPD) patients. Exhaled nitric oxide (FeNO(50) (exhaled NO at a flow rate of 50mL/s)), FeNO(200) and CaNO (peripheral concentration of NO/alveolar NO) and clinical variables including pulmonary function, COPD Assessment Test (CAT), C-reactive protein concentration (CRP) and circulating eosinophil count were measured among the recruited participants. FeNO(50,) FeNO(200) and CaNO were repeatedly evaluated in 39 AECOPD patients after corticosteroid treatment. RESULTS: FeNO(200) was significantly higher in stable COPD and AECOPD patients than in healthy controls. Nevertheless, CaNO could not differentiate COPD from healthy controls. No correlation was found between circulating eosinophil counts or FEV1 and exhaled nitric oxide (FeNO(50,) FeNO(200), CaNO) in COPD patients. For AECOPD patients, 64% of patients had eosinophil counts >100 cells/µL; 59% of patients had FeNO(200) >10 ppb; only 31% of patients had FeNO(50) > 25 ppb. Among AECOPD patients, the high FeNO(50) and FeNO(200) groups’ levels were significantly lower than their baseline levels, and significant improvements in CAT were seen in the two groups after corticosteroid treatment. These implied a good corticosteroid response in AECOPD patients with FeNO(200)>10ppb. CONCLUSION: FeNO(200) is a straightforward and feasible method to evaluate the peripheral NO concentration in COPD. FeNO200 can be a type 2 inflammation biomarker and a useful tool for predicting corticosteroid therapy in COPD.
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spelling pubmed-79140662021-03-01 Clinical Utility of Central and Peripheral Airway Nitric Oxide in Aging Patients with Stable and Acute Exacerbated Chronic Obstructive Pulmonary Disease Fan, Xiaodong Zhao, Nian Yu, Zhen Yu, Haoda Yin, Bo Zou, Lifei Zhao, Yinying Qian, Xiufen Sai, Xiaoyan Qin, Chu Fu, Congli Hu, Caixia Di, Tingting Yang, Yue Wu, Yan Bian, Tao Int J Gen Med Original Research PURPOSE: Exhaled nitric oxide has been used as a marker of airway inflammation. The NO concentration in the central and peripheral airway/alveolar can be measured by a slow and fast exhalation flow rate to evaluate inflammation in different divisions within the respiratory tract. We hypothesized that FeNO(200) (exhaled NO at a flow rate of 200mL/s) could be used as an evaluation tool for peripheral airway/alveolar inflammation and corticosteroid therapy in chronic obstructive pulmonary disease (COPD) patients. METHODS: We recruited 171 subjects into the study: 73 healthy controls, 59 stable COPD patients, and 39 acute exacerbations of COPD (AECOPD) patients. Exhaled nitric oxide (FeNO(50) (exhaled NO at a flow rate of 50mL/s)), FeNO(200) and CaNO (peripheral concentration of NO/alveolar NO) and clinical variables including pulmonary function, COPD Assessment Test (CAT), C-reactive protein concentration (CRP) and circulating eosinophil count were measured among the recruited participants. FeNO(50,) FeNO(200) and CaNO were repeatedly evaluated in 39 AECOPD patients after corticosteroid treatment. RESULTS: FeNO(200) was significantly higher in stable COPD and AECOPD patients than in healthy controls. Nevertheless, CaNO could not differentiate COPD from healthy controls. No correlation was found between circulating eosinophil counts or FEV1 and exhaled nitric oxide (FeNO(50,) FeNO(200), CaNO) in COPD patients. For AECOPD patients, 64% of patients had eosinophil counts >100 cells/µL; 59% of patients had FeNO(200) >10 ppb; only 31% of patients had FeNO(50) > 25 ppb. Among AECOPD patients, the high FeNO(50) and FeNO(200) groups’ levels were significantly lower than their baseline levels, and significant improvements in CAT were seen in the two groups after corticosteroid treatment. These implied a good corticosteroid response in AECOPD patients with FeNO(200)>10ppb. CONCLUSION: FeNO(200) is a straightforward and feasible method to evaluate the peripheral NO concentration in COPD. FeNO200 can be a type 2 inflammation biomarker and a useful tool for predicting corticosteroid therapy in COPD. Dove 2021-02-23 /pmc/articles/PMC7914066/ /pubmed/33654424 http://dx.doi.org/10.2147/IJGM.S284688 Text en © 2021 Fan et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Fan, Xiaodong
Zhao, Nian
Yu, Zhen
Yu, Haoda
Yin, Bo
Zou, Lifei
Zhao, Yinying
Qian, Xiufen
Sai, Xiaoyan
Qin, Chu
Fu, Congli
Hu, Caixia
Di, Tingting
Yang, Yue
Wu, Yan
Bian, Tao
Clinical Utility of Central and Peripheral Airway Nitric Oxide in Aging Patients with Stable and Acute Exacerbated Chronic Obstructive Pulmonary Disease
title Clinical Utility of Central and Peripheral Airway Nitric Oxide in Aging Patients with Stable and Acute Exacerbated Chronic Obstructive Pulmonary Disease
title_full Clinical Utility of Central and Peripheral Airway Nitric Oxide in Aging Patients with Stable and Acute Exacerbated Chronic Obstructive Pulmonary Disease
title_fullStr Clinical Utility of Central and Peripheral Airway Nitric Oxide in Aging Patients with Stable and Acute Exacerbated Chronic Obstructive Pulmonary Disease
title_full_unstemmed Clinical Utility of Central and Peripheral Airway Nitric Oxide in Aging Patients with Stable and Acute Exacerbated Chronic Obstructive Pulmonary Disease
title_short Clinical Utility of Central and Peripheral Airway Nitric Oxide in Aging Patients with Stable and Acute Exacerbated Chronic Obstructive Pulmonary Disease
title_sort clinical utility of central and peripheral airway nitric oxide in aging patients with stable and acute exacerbated chronic obstructive pulmonary disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7914066/
https://www.ncbi.nlm.nih.gov/pubmed/33654424
http://dx.doi.org/10.2147/IJGM.S284688
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