Fractional Exhaled Nitric Oxide as an Inflammatory Biomarker in Chronic Obstructive Pulmonary Disease (COPD) with or without Concurrent Diagnosis of Asthma: The Canadian Cohort Obstructive Lung Disease (CanCOLD)

COPD: Journal of Chronic Obstructive Pulmonary Disease, 2020

Posted: 17 Jul 2020

See all articles by Seyed-Mohammad-Yousof Mostafavi-Pour-Manshadi

Seyed-Mohammad-Yousof Mostafavi-Pour-Manshadi

Respiratory Epidemiology and Clinical Research Unit, Research Institute of McGill University Health Centre, McGill University, Montreal, Canada

Nafiseh Naderi

McGill University - Division of Experimental Medicine; Respiratory Epidemiology and Clinical Research Unit, Research Institute of McGill University Health Centre, McGill University, Montreal, Canada

Palmina Mancino

McGill University - Respiratory Epidemiology and Clinical Research Unit

Pei Zhi Li

Independent

Wan Tan

UBC Centre for Heart Lung Innovation, St Paul’s Hospital

Jean Bourbeau

Respiratory Epidemiology and Clinical Research Unit, Research Institute of McGill University Health Centre, McGill University, Montreal, Canada

Date Written: June 25, 2020

Abstract

We studied whether fractional exhaled nitric oxide (FENO) can differentiate chronic obstructive ‎pulmonary disease (COPD) with concurrent diagnosis of asthma from COPD-only as well as its ‎ability to predict disease severity and progression. ‎

This study was embedded in the Canadian Cohort Obstructive Lung Disease (CanCOLD).‎

Subjects of ≥40 years old completed FENO measurements were subdivided into four groups, ‎including COPD (N=86 [COPD-only (N=35) and COPD with concurrent diagnosis of asthma ‎‎(N=51)], healthy (N=72), and at risk (N=151). Three of the most common clinical definitions ‎were used for characterizing COPD with concurrent diagnosis of asthma: 1) atopy and self-‎reported physician diagnosis of asthma, 2) ≥12% and ≥200 ml post-bronchodilator FEV1; 3) ‎self-reported physician diagnosis of asthma. FENO values were classified using quartiles and the ‎American Thoracic Society (ATS) guideline 2011. ‎

Compared to COPD-only, more COPD with concurrent diagnosis of asthma had a significant ‎FENO50 ≥ 33.5 ppb (fourth quartile) than COPD-only (p=0.045, 0.011, and 0.006, for definition ‎‎1, 2, and 3, respectively). Considering the ATS guideline 2011, fewer COPD with concurrent ‎diagnosis of asthma had FENO50 < 25 than COPD-only, which was statistically significant with ‎definition 1 and 3 (p=0.038 and 0.026, respectively).‎

FENO as a biomarker has the potential to be used as a complementary value for differentiating ‎COPD with concurrent diagnosis of asthma from COPD-only. Further studies should be ‎conducted on validated definitions of COPD with concurrent diagnosis of asthma, which may ‎include a reference to the type of airway inflammation in addition to the clinical definition. ‎

Keywords: Fractional Exhaled Nitric Oxide, Chronic Obstructive Pulmonary Disease, COPD, Asthma, ‎Canadian Cohort Obstructive Lung Disease, CanCOLD

Suggested Citation

Mostafavi-Pour-Manshadi, Seyed-Mohammad-Yousof and Naderi, Nafiseh and Mancino, Palmina and Li, Pei Zhi and Tan, Wan and Bourbeau, Jean, Fractional Exhaled Nitric Oxide as an Inflammatory Biomarker in Chronic Obstructive Pulmonary Disease (COPD) with or without Concurrent Diagnosis of Asthma: The Canadian Cohort Obstructive Lung Disease (CanCOLD) (June 25, 2020). COPD: Journal of Chronic Obstructive Pulmonary Disease, 2020, Available at SSRN: https://ssrn.com/abstract=3635886

Seyed-Mohammad-Yousof Mostafavi-Pour-Manshadi (Contact Author)

Respiratory Epidemiology and Clinical Research Unit, Research Institute of McGill University Health Centre, McGill University, Montreal, Canada ( email )

Montreal, Quebec
Canada

Nafiseh Naderi

McGill University - Division of Experimental Medicine ( email )

Montreal, Quebec
Canada

Respiratory Epidemiology and Clinical Research Unit, Research Institute of McGill University Health Centre, McGill University, Montreal, Canada ( email )

Palmina Mancino

McGill University - Respiratory Epidemiology and Clinical Research Unit ( email )

Montreal, Quebec
Canada

Pei Zhi Li

Independent ( email )

Wan Tan

UBC Centre for Heart Lung Innovation, St Paul’s Hospital ( email )

Vancouver, British-Columbia
Canada

Jean Bourbeau

Respiratory Epidemiology and Clinical Research Unit, Research Institute of McGill University Health Centre, McGill University, Montreal, Canada ( email )

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