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Relationship between alveolar nitric oxide concentration in exhaled air and small airway function in COPD

Nitrative stress is thought to be involved in the inflammatory process in COPD airways, and the alveolar nitric oxide concentration (CAlv) has been reported to be increased. However, the CAlv levels are also regulated by gas diffusion at alveolar sites. The aim of the study was to assess the relatio...

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Published in:Journal of breath research 2013-12, Vol.7 (4), p.046002-046002
Main Authors: Hirano, Tsunahiko, Matsunaga, Kazuto, Sugiura, Hisatoshi, Minakata, Yoshiaki, Koarai, Akira, Akamatsu, Keiichiro, Ichikawa, Tomohiro, Furukawa, Kanako, Ichinose, Masakazu
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creator Hirano, Tsunahiko
Matsunaga, Kazuto
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Ichinose, Masakazu
description Nitrative stress is thought to be involved in the inflammatory process in COPD airways, and the alveolar nitric oxide concentration (CAlv) has been reported to be increased. However, the CAlv levels are also regulated by gas diffusion at alveolar sites. The aim of the study was to assess the relationship between the CAlv and pulmonary function in COPD patients, while taking into account the lung diffusion capacity. Twenty stable COPD patients (GOLD stage1 2 3 4 = 6 8 6 0) and 16 healthy subjects took part in this cross-sectional study. Fractional exhaled nitric oxide (FENO), CAlv, and pulmonary functions were measured. Pulmonary function, including single nitrogen washout curve (dN2) and diffusion capacity for carbon monoxide (DLCO), was also evaluated in patients with COPD. The mean FENO levels (20.7 ppb versus 16.3 ppb, p < 0.05) and the mean CAlv levels (6.4 ppb versus 4.2 ppb, p < 0.01) in COPD patients were significantly increased compared to those in HS. The CAlv level in COPD was significantly correlated with dN2, %DLCO alveolar volume (VA). Using the standard entry method of multivariate analysis to adjust for dN2 and %DLCO VA, dN2 (β = 0.54, p = 0.005) and %DLCO VA (β = −0.44, p = 0.018) still showed significant correlations with the CAlv levels. These results suggest that the CAlv could be a useful marker for the small airway dysfunction in COPD. Airway inflammation, including excess nitric oxide generation in the peripheral airways, might be related to the pathophysiology of COPD.
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However, the CAlv levels are also regulated by gas diffusion at alveolar sites. The aim of the study was to assess the relationship between the CAlv and pulmonary function in COPD patients, while taking into account the lung diffusion capacity. Twenty stable COPD patients (GOLD stage1 2 3 4 = 6 8 6 0) and 16 healthy subjects took part in this cross-sectional study. Fractional exhaled nitric oxide (FENO), CAlv, and pulmonary functions were measured. Pulmonary function, including single nitrogen washout curve (dN2) and diffusion capacity for carbon monoxide (DLCO), was also evaluated in patients with COPD. The mean FENO levels (20.7 ppb versus 16.3 ppb, p &lt; 0.05) and the mean CAlv levels (6.4 ppb versus 4.2 ppb, p &lt; 0.01) in COPD patients were significantly increased compared to those in HS. The CAlv level in COPD was significantly correlated with dN2, %DLCO alveolar volume (VA). Using the standard entry method of multivariate analysis to adjust for dN2 and %DLCO VA, dN2 (β = 0.54, p = 0.005) and %DLCO VA (β = −0.44, p = 0.018) still showed significant correlations with the CAlv levels. These results suggest that the CAlv could be a useful marker for the small airway dysfunction in COPD. 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Breath Res</addtitle><description>Nitrative stress is thought to be involved in the inflammatory process in COPD airways, and the alveolar nitric oxide concentration (CAlv) has been reported to be increased. However, the CAlv levels are also regulated by gas diffusion at alveolar sites. The aim of the study was to assess the relationship between the CAlv and pulmonary function in COPD patients, while taking into account the lung diffusion capacity. Twenty stable COPD patients (GOLD stage1 2 3 4 = 6 8 6 0) and 16 healthy subjects took part in this cross-sectional study. Fractional exhaled nitric oxide (FENO), CAlv, and pulmonary functions were measured. Pulmonary function, including single nitrogen washout curve (dN2) and diffusion capacity for carbon monoxide (DLCO), was also evaluated in patients with COPD. 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Breath Res</addtitle><date>2013-12-01</date><risdate>2013</risdate><volume>7</volume><issue>4</issue><spage>046002</spage><epage>046002</epage><pages>046002-046002</pages><issn>1752-7155</issn><eissn>1752-7163</eissn><coden>JBROBW</coden><abstract>Nitrative stress is thought to be involved in the inflammatory process in COPD airways, and the alveolar nitric oxide concentration (CAlv) has been reported to be increased. However, the CAlv levels are also regulated by gas diffusion at alveolar sites. The aim of the study was to assess the relationship between the CAlv and pulmonary function in COPD patients, while taking into account the lung diffusion capacity. Twenty stable COPD patients (GOLD stage1 2 3 4 = 6 8 6 0) and 16 healthy subjects took part in this cross-sectional study. Fractional exhaled nitric oxide (FENO), CAlv, and pulmonary functions were measured. Pulmonary function, including single nitrogen washout curve (dN2) and diffusion capacity for carbon monoxide (DLCO), was also evaluated in patients with COPD. The mean FENO levels (20.7 ppb versus 16.3 ppb, p &lt; 0.05) and the mean CAlv levels (6.4 ppb versus 4.2 ppb, p &lt; 0.01) in COPD patients were significantly increased compared to those in HS. The CAlv level in COPD was significantly correlated with dN2, %DLCO alveolar volume (VA). Using the standard entry method of multivariate analysis to adjust for dN2 and %DLCO VA, dN2 (β = 0.54, p = 0.005) and %DLCO VA (β = −0.44, p = 0.018) still showed significant correlations with the CAlv levels. These results suggest that the CAlv could be a useful marker for the small airway dysfunction in COPD. Airway inflammation, including excess nitric oxide generation in the peripheral airways, might be related to the pathophysiology of COPD.</abstract><cop>England</cop><pub>IOP Publishing</pub><pmid>24091810</pmid><doi>10.1088/1752-7155/7/4/046002</doi><tpages>6</tpages></addata></record>
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subjects Aged
alveolar NO
Biomarkers - analysis
Breath Tests - methods
Chronic obstructive pulmonary disease
COPD
diffusion capacity
Exhalation
Female
Humans
Male
Nitric oxide
Nitric Oxide - analysis
Pulmonary Alveoli - metabolism
Pulmonary Alveoli - physiopathology
Pulmonary Disease, Chronic Obstructive - metabolism
pulmonary function
title Relationship between alveolar nitric oxide concentration in exhaled air and small airway function in COPD
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