Bronchodilator response and lung function decline: Associations with exhaled nitric oxide with regard to sex and smoking status

Fractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma patients. The associations of FeNO with lung function decline and bronchodilator (BD) response have been studied only scarcely in large populations. To study the as...

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Published inThe World Allergy Organization journal Vol. 14; no. 5; p. 100544
Main Authors Nerpin, Elisabet, Ferreira, Diogenes Seraphim, Weyler, Joost, Schlunnsen, Vivi, Jogi, Rain, Raherison Semjen, Chantal, Gislasson, Thorainn, Demoly, Pascal, Heinrich, Joachim, Nowak, Dennis, Corsico, Angelo, Accordini, Simone, Marcon, Alessandro, Squillacioti, Giulia, Olivieri, Mario, Nielsen, Rune, Johannessen, Ane, Gómez Real, Francisco, Garcia -Aymerich, Judith, Urrutia, Isabel, Pereira-Vega, Antonio, Gullón, Jose Antonio, Olin, Anna-Carin, Forsberg, Bertil, Emilsson, Össur Ingi, Pin, Isabelle, Jarvis, Deborah, Janson, Christer, Malinovschi, Andrei
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.05.2021
Elsevier BV
Elsevier
World Allergy Organization
Subjects
Online AccessGet full text
ISSN1939-4551
1939-4551
DOI10.1016/j.waojou.2021.100544

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Abstract Fractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma patients. The associations of FeNO with lung function decline and bronchodilator (BD) response have been studied only scarcely in large populations. To study the association between FeNO and a) retrospective lung function decline over 20 years, and b) lung function response to BD among asthmatic subjects compared with non-asthmatic subjects and with regards to current smoking and sex. Longitudinal analyses of previous lung function decline and FeNO level at follow-up and cross-sectional analyses of BD response and FeNO levels in 4257 participants (651 asthmatics) from the European Community Respiratory Health Survey. Among asthmatic subjects, higher percentage declines of FEV1 and FEV1/FVC were associated with higher FeNO levels (p = 0.001 for both) at follow-up. These correlations were found mainly among non-smoking individuals (p = 0.001) and females (p = 0.001) in stratified analyses. Percentage increase in FEV1 after BD was positively associated with FeNO levels in non-asthmatic subjects. Further, after stratified for sex and smoking separately, a positive association was seen between FEV1 and FeNO levels in non-smokers and women, regardless of asthma status. We found a relationship between elevated FeNO and larger FEV1 decline over 20 years among subjects with asthma who were non-smokers or women. The association between elevated FeNO levels and larger BD response was found in both non-asthmatic and asthmatic subjects, mainly in women and non-smoking subjects.
AbstractList Background: Fractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma patients.The associations of FeNO with lung function decline and bronchodilator (BD) response have been studied only scarcely in large populations. Objectives: To study the association between FeNO and a) retrospective lung function decline over 20 years, and b) lung function response to BD among asthmatic subjects compared with non-asthmatic subjects and with regards to current smoking and sex. Methods: Longitudinal analyses of previous lung function decline and FeNO level at follow-up and cross-sectional analyses of BD response and FeNO levels in 4257 participants (651 asthmatics) from the European Community Respiratory Health Survey. Results: Among asthmatic subjects, higher percentage declines of FEV1 and FEV1/FVC were associated with higher FeNO levels (p = 0.001 for both) atfollow-up.These correlations were found mainly among non-smoking individuals (p = 0.001) and females (p = 0.001) in stratified analyses. Percentage increase in FEV1 after BD was positively associated with FeNO levels in non-asthmatic subjects. Further, after stratified for sex and smoking separately, a positive association was seen between FEV(1 )and FeNO levels in non-smokers and women, regardless of asthma status. Conclusions: We found a relationship between elevated FeNO and larger FEV1 decline over 20 years among subjects with asthma who were non-smokers or women. The association between elevated FeNO levels and larger BD response was found in both non-asthmatic and asthmatic subjects, mainly in women and non-smoking subjects.
BACKGROUND: Fractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma patients. The associations of FeNO with lung function decline and bronchodilator (BD) response have been studied only scarcely in large populations. OBJECTIVES: To study the association between FeNO and a) retrospective lung function decline over 20 years, and b) lung function response to BD among asthmatic subjects compared with non-asthmatic subjects and with regards to current smoking and sex. METHODS: Longitudinal analyses of previous lung function decline and FeNO level at follow-up and cross-sectional analyses of BD response and FeNO levels in 4257 participants (651 asthmatics) from the European Community Respiratory Health Survey. RESULTS: Among asthmatic subjects, higher percentage declines of FEV(1) and FEV(1)/FVC were associated with higher FeNO levels (p = 0.001 for both) at follow-up. These correlations were found mainly among non-smoking individuals (p = 0.001) and females (p = 0.001) in stratified analyses.Percentage increase in FEV(1) after BD was positively associated with FeNO levels in non-asthmatic subjects. Further, after stratified for sex and smoking separately, a positive association was seen between FEV(1) and FeNO levels in non-smokers and women, regardless of asthma status. CONCLUSIONS: We found a relationship between elevated FeNO and larger FEV(1) decline over 20 years among subjects with asthma who were non-smokers or women. The association between elevated FeNO levels and larger BD response was found in both non-asthmatic and asthmatic subjects, mainly in women and non-smoking subjects.
Fractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma patients. The associations of FeNO with lung function decline and bronchodilator (BD) response have been studied only scarcely in large populations. To study the association between FeNO and a) retrospective lung function decline over 20 years, and b) lung function response to BD among asthmatic subjects compared with non-asthmatic subjects and with regards to current smoking and sex. Longitudinal analyses of previous lung function decline and FeNO level at follow-up and cross-sectional analyses of BD response and FeNO levels in 4257 participants (651 asthmatics) from the European Community Respiratory Health Survey. Among asthmatic subjects, higher percentage declines of FEV and FEV /FVC were associated with higher FeNO levels (p = 0.001 for both) at follow-up. These correlations were found mainly among non-smoking individuals (p = 0.001) and females (p = 0.001) in stratified analyses.Percentage increase in FEV after BD was positively associated with FeNO levels in non-asthmatic subjects. Further, after stratified for sex and smoking separately, a positive association was seen between FEV and FeNO levels in non-smokers and women, regardless of asthma status. We found a relationship between elevated FeNO and larger FEV decline over 20 years among subjects with asthma who were non-smokers or women. The association between elevated FeNO levels and larger BD response was found in both non-asthmatic and asthmatic subjects, mainly in women and non-smoking subjects.
Fractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma patients. The associations of FeNO with lung function decline and bronchodilator (BD) response have been studied only scarcely in large populations. To study the association between FeNO and a) retrospective lung function decline over 20 years, and b) lung function response to BD among asthmatic subjects compared with non-asthmatic subjects and with regards to current smoking and sex. Longitudinal analyses of previous lung function decline and FeNO level at follow-up and cross-sectional analyses of BD response and FeNO levels in 4257 participants (651 asthmatics) from the European Community Respiratory Health Survey. Among asthmatic subjects, higher percentage declines of FEV1 and FEV1/FVC were associated with higher FeNO levels (p = 0.001 for both) at follow-up. These correlations were found mainly among non-smoking individuals (p = 0.001) and females (p = 0.001) in stratified analyses. Percentage increase in FEV1 after BD was positively associated with FeNO levels in non-asthmatic subjects. Further, after stratified for sex and smoking separately, a positive association was seen between FEV1 and FeNO levels in non-smokers and women, regardless of asthma status. We found a relationship between elevated FeNO and larger FEV1 decline over 20 years among subjects with asthma who were non-smokers or women. The association between elevated FeNO levels and larger BD response was found in both non-asthmatic and asthmatic subjects, mainly in women and non-smoking subjects.
Fractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma patients. The associations of FeNO with lung function decline and bronchodilator (BD) response have been studied only scarcely in large populations.BACKGROUNDFractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma patients. The associations of FeNO with lung function decline and bronchodilator (BD) response have been studied only scarcely in large populations.To study the association between FeNO and a) retrospective lung function decline over 20 years, and b) lung function response to BD among asthmatic subjects compared with non-asthmatic subjects and with regards to current smoking and sex.OBJECTIVESTo study the association between FeNO and a) retrospective lung function decline over 20 years, and b) lung function response to BD among asthmatic subjects compared with non-asthmatic subjects and with regards to current smoking and sex.Longitudinal analyses of previous lung function decline and FeNO level at follow-up and cross-sectional analyses of BD response and FeNO levels in 4257 participants (651 asthmatics) from the European Community Respiratory Health Survey.METHODSLongitudinal analyses of previous lung function decline and FeNO level at follow-up and cross-sectional analyses of BD response and FeNO levels in 4257 participants (651 asthmatics) from the European Community Respiratory Health Survey.Among asthmatic subjects, higher percentage declines of FEV1 and FEV1/FVC were associated with higher FeNO levels (p = 0.001 for both) at follow-up. These correlations were found mainly among non-smoking individuals (p = 0.001) and females (p = 0.001) in stratified analyses.Percentage increase in FEV1 after BD was positively associated with FeNO levels in non-asthmatic subjects. Further, after stratified for sex and smoking separately, a positive association was seen between FEV1 and FeNO levels in non-smokers and women, regardless of asthma status.RESULTSAmong asthmatic subjects, higher percentage declines of FEV1 and FEV1/FVC were associated with higher FeNO levels (p = 0.001 for both) at follow-up. These correlations were found mainly among non-smoking individuals (p = 0.001) and females (p = 0.001) in stratified analyses.Percentage increase in FEV1 after BD was positively associated with FeNO levels in non-asthmatic subjects. Further, after stratified for sex and smoking separately, a positive association was seen between FEV1 and FeNO levels in non-smokers and women, regardless of asthma status.We found a relationship between elevated FeNO and larger FEV1 decline over 20 years among subjects with asthma who were non-smokers or women. The association between elevated FeNO levels and larger BD response was found in both non-asthmatic and asthmatic subjects, mainly in women and non-smoking subjects.CONCLUSIONSWe found a relationship between elevated FeNO and larger FEV1 decline over 20 years among subjects with asthma who were non-smokers or women. The association between elevated FeNO levels and larger BD response was found in both non-asthmatic and asthmatic subjects, mainly in women and non-smoking subjects.
Background: Fractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma patients.The associations of FeNO with lung function decline and bronchodilator (BD) response have been studied only scarcely in large populations. Objectives: To study the association between FeNO and a) retrospective lung function decline over 20 years, and b) lung function response to BD among asthmatic subjects compared with non-asthmatic subjects and with regards to current smoking and sex. Methods: Longitudinal analyses of previous lung function decline and FeNO level at follow-up and cross-sectional analyses of BD response and FeNO levels in 4257 participants (651 asthmatics) from the European Community Respiratory Health Survey. Results: Among asthmatic subjects, higher percentage declines of FEV1 and FEV1/FVC were associated with higher FeNO levels (p = 0.001 for both) atfollow-up.These correlations were found mainly among non-smoking individuals (p = 0.001) and females (p = 0.001) in stratified analyses. Percentage increase in FEV1 after BD was positively associated with FeNO levels in non-asthmatic subjects. Further, after stratified for sex and smoking separately, a positive association was seen between FEV(1 )and FeNO levels in non-smokers and women, regardless of asthma status. Conclusions: We found a relationship between elevated FeNO and larger FEV1 decline over 20 years among subjects with asthma who were non-smokers or women. The association between elevated FeNO levels and larger BD response was found in both non-asthmatic and asthmatic subjects, mainly in women and non-smoking subjects.
Background: Fractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma patients. The associations of FeNO with lung function decline and bronchodilator (BD) response have been studied only scarcely in large populations. Objectives: To study the association between FeNO and a) retrospective lung function decline over 20 years, and b) lung function response to BD among asthmatic subjects compared with non-asthmatic subjects and with regards to current smoking and sex. Methods: Longitudinal analyses of previous lung function decline and FeNO level at follow-up and cross-sectional analyses of BD response and FeNO levels in 4257 participants (651 asthmatics) from the European Community Respiratory Health Survey. Results: Among asthmatic subjects, higher percentage declines of FEV1 and FEV1/FVC were associated with higher FeNO levels (p = 0.001 for both) at follow-up. These correlations were found mainly among non-smoking individuals (p = 0.001) and females (p = 0.001) in stratified analyses.Percentage increase in FEV1 after BD was positively associated with FeNO levels in non-asthmatic subjects. Further, after stratified for sex and smoking separately, a positive association was seen between FEV1 and FeNO levels in non-smokers and women, regardless of asthma status. Conclusions: We found a relationship between elevated FeNO and larger FEV1 decline over 20 years among subjects with asthma who were non-smokers or women. The association between elevated FeNO levels and larger BD response was found in both non-asthmatic and asthmatic subjects, mainly in women and non-smoking subjects.
Background: Fractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma patients. The associations of FeNO with lung function decline and bronchodilator (BD) response have been studied only scarcely in large populations. Objectives: To study the association between FeNO and a) retrospective lung function decline over 20 years, and b) lung function response to BD among asthmatic subjects compared with non-asthmatic subjects and with regards to current smoking and sex. Methods: Longitudinal analyses of previous lung function decline and FeNO level at follow-up and cross-sectional analyses of BD response and FeNO levels in 4257 participants (651 asthmatics) from the European Community Respiratory Health Survey. Results: Among asthmatic subjects, higher percentage declines of FEV1 and FEV1/FVC were associated with higher FeNO levels (p = 0.001 for both) at follow-up. These correlations were found mainly among non-smoking individuals (p = 0.001) and females (p = 0.001) in stratified analyses. Percentage increase in FEV1 after BD was positively associated with FeNO levels in non-asthmatic subjects. Further, after stratified for sex and smoking separately, a positive association was seen between FEV1 and FeNO levels in non-smokers and women, regardless of asthma status. Conclusions: We found a relationship between elevated FeNO and larger FEV1 decline over 20 years among subjects with asthma who were non-smokers or women. The association between elevated FeNO levels and larger BD response was found in both non-asthmatic and asthmatic subjects, mainly in women and non-smoking subjects.
BackgroundFractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma patients. The associations of FeNO with lung function decline and bronchodilator (BD) response have been studied only scarcely in large populations.ObjectivesTo study the association between FeNO and a) retrospective lung function decline over 20 years, and b) lung function response to BD among asthmatic subjects compared with non-asthmatic subjects and with regards to current smoking and sex.MethodsLongitudinal analyses of previous lung function decline and FeNO level at follow-up and cross-sectional analyses of BD response and FeNO levels in 4257 participants (651 asthmatics) from the European Community Respiratory Health Survey.ResultsAmong asthmatic subjects, higher percentage declines of FEV1 and FEV1/FVC were associated with higher FeNO levels (p = 0.001 for both) at follow-up. These correlations were found mainly among non-smoking individuals (p = 0.001) and females (p = 0.001) in stratified analyses.Percentage increase in FEV1 after BD was positively associated with FeNO levels in non-asthmatic subjects. Further, after stratified for sex and smoking separately, a positive association was seen between FEV1 and FeNO levels in non-smokers and women, regardless of asthma status.ConclusionsWe found a relationship between elevated FeNO and larger FEV1 decline over 20 years among subjects with asthma who were non-smokers or women. The association between elevated FeNO levels and larger BD response was found in both non-asthmatic and asthmatic subjects, mainly in women and non-smoking subjects.
ArticleNumber 100544
Author Marcon, Alessandro
Weyler, Joost
Jogi, Rain
Nerpin, Elisabet
Gómez Real, Francisco
Corsico, Angelo
Olin, Anna-Carin
Olivieri, Mario
Pin, Isabelle
Janson, Christer
Heinrich, Joachim
Accordini, Simone
Demoly, Pascal
Gullón, Jose Antonio
Forsberg, Bertil
Squillacioti, Giulia
Pereira-Vega, Antonio
Ferreira, Diogenes Seraphim
Garcia -Aymerich, Judith
Nowak, Dennis
Nielsen, Rune
Gislasson, Thorainn
Malinovschi, Andrei
Jarvis, Deborah
Urrutia, Isabel
Schlunnsen, Vivi
Emilsson, Össur Ingi
Raherison Semjen, Chantal
Johannessen, Ane
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  orcidid: 0000-0003-3880-2132
  surname: Nerpin
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  email: ene@du.se
  organization: Department of Medical Sciences, Respiratory Medicine, Allergy and Sleep, Uppsala University, Uppsala, Sweden
– sequence: 2
  givenname: Diogenes Seraphim
  surname: Ferreira
  fullname: Ferreira, Diogenes Seraphim
  organization: Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Melbourne, Australia
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  givenname: Joost
  surname: Weyler
  fullname: Weyler, Joost
  organization: Epidemiology and Social Medicine, University of Antwerp, Antwerp, Belgium
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  givenname: Vivi
  surname: Schlunnsen
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  organization: Department of Environment Occupation & Health, Danish Ramazzini Centre, Aarhus University, Aarhus, Denmark
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  givenname: Rain
  surname: Jogi
  fullname: Jogi, Rain
  organization: Lung Clinic, Tartu University Hospital, Tartu, Estonia
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  organization: U1219, Bordeaux Population Health Research Center, Bordeaux, France
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  givenname: Thorainn
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  organization: Department of Sleep, Landspitali University Hospital, Reykjavik, Iceland
– sequence: 8
  givenname: Pascal
  surname: Demoly
  fullname: Demoly, Pascal
  organization: Département de Pneumologie et Addictologie, Centre Hospitalier Universitaire de Montpellier, Hopital Arnaud de Villeneuve, Univ Montpellier, Montpellier, France
– sequence: 9
  givenname: Joachim
  surname: Heinrich
  fullname: Heinrich, Joachim
  organization: Institute and Outpatient Clinic for Occupational, Social and Environmental Medicine, University Hospital Munich, Ludwig Maximilians University Munich, Munich, Germany
– sequence: 10
  givenname: Dennis
  surname: Nowak
  fullname: Nowak, Dennis
  organization: Hospital of the Ludwig-Maximilian University Munich, LMU Munich, Munich, Germany
– sequence: 11
  givenname: Angelo
  surname: Corsico
  fullname: Corsico, Angelo
  organization: Division of Respiratory Diseases, Medical Sciences and Infectious Diseases Department, IRCCS Policlinico San Matteo Foundation
– sequence: 12
  givenname: Simone
  surname: Accordini
  fullname: Accordini, Simone
  organization: Unit of Epidemiology and Medical Statistics, Department of Diagnostics and Public Health, University of Verona, Verona, Italy
– sequence: 13
  givenname: Alessandro
  surname: Marcon
  fullname: Marcon, Alessandro
  organization: Unit of Epidemiology and Medical Statistics, Department of Diagnostics and Public Health, University of Verona, Verona, Italy
– sequence: 14
  givenname: Giulia
  surname: Squillacioti
  fullname: Squillacioti, Giulia
  organization: Department of Public Health and Pediatrics - University of Turin, Turin, Italy
– sequence: 15
  givenname: Mario
  surname: Olivieri
  fullname: Olivieri, Mario
  organization: Unit of Occupational Medicine, Department of Diagnostics and Public Health, University of Verona, Verona, Italy
– sequence: 16
  givenname: Rune
  surname: Nielsen
  fullname: Nielsen, Rune
  organization: Department of Thoracic Medicine, Haukeland University Hospital, Bergen, Norway
– sequence: 17
  givenname: Ane
  surname: Johannessen
  fullname: Johannessen, Ane
  organization: Department of Global Public Health and Primary Care, Centre for International Health, University of Bergen, Bergen, Norway
– sequence: 18
  givenname: Francisco
  surname: Gómez Real
  fullname: Gómez Real, Francisco
  organization: Department of Clinical Science, University of Bergen, Bergen, Norway
– sequence: 19
  givenname: Judith
  surname: Garcia -Aymerich
  fullname: Garcia -Aymerich, Judith
  organization: ISGlobAL, Centre for Research in Environmental Epidemiology (CREAL), Barcelona, Spain
– sequence: 20
  givenname: Isabel
  surname: Urrutia
  fullname: Urrutia, Isabel
  organization: Pneumology Service of Galdakao Hospital in Bizkaia, Spain
– sequence: 21
  givenname: Antonio
  surname: Pereira-Vega
  fullname: Pereira-Vega, Antonio
  organization: Pneumology and Allergy Service of the Juan Ramón Jiménez Hospital in Huelva, Spain
– sequence: 22
  givenname: Jose Antonio
  surname: Gullón
  fullname: Gullón, Jose Antonio
  organization: Peumology. San Agustín Universitary Hospital, Avilés, Spain
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  givenname: Anna-Carin
  surname: Olin
  fullname: Olin, Anna-Carin
  organization: Section of Occupational and Environmental Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
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  givenname: Bertil
  surname: Forsberg
  fullname: Forsberg, Bertil
  organization: Sustainable Health, Department of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden
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  givenname: Össur Ingi
  surname: Emilsson
  fullname: Emilsson, Össur Ingi
  organization: Department of Medical Sciences, Respiratory Medicine, Allergy and Sleep, Uppsala University, Uppsala, Sweden
– sequence: 26
  givenname: Isabelle
  surname: Pin
  fullname: Pin, Isabelle
  organization: CHU Grenoble Alpes, Inserm, Institut for Advanced Biosciences, Grenoble Alpes University, Grenoble, France
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  givenname: Deborah
  surname: Jarvis
  fullname: Jarvis, Deborah
  organization: National Heart and Lung Institute, Imperial College London, London, UK
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  givenname: Christer
  surname: Janson
  fullname: Janson, Christer
  organization: Department of Medical Sciences, Respiratory Medicine, Allergy and Sleep, Uppsala University, Uppsala, Sweden
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  givenname: Andrei
  surname: Malinovschi
  fullname: Malinovschi, Andrei
  organization: Department of Medical Sciences: Clinical Physiology, Uppsala University, Uppsala, Sweden
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Issue 5
Keywords FeNO
Bronchodilatation
Lung function
Epidemiology
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Snippet Fractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma patients. The...
BackgroundFractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma patients. The...
BACKGROUND: Fractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma patients....
Background: Fractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma patients....
Background: Fractional exhaled nitric oxide (FeNO) is a marker of type-2 inflammation used both to support diagnosis of asthma and follow up asthma...
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StartPage 100544
SubjectTerms Allergies
Asthma
Bronchodilatation
Bronchodilators
Chronic obstructive pulmonary disease
Clinical Medicine
Epidemiology
FeNO
Hay fever
Immunoglobulins
Inflammation
Klinisk medicin
Life Sciences
Lung function
Nitric oxide
Questionnaires
Santé publique et épidémiologie
Self report
Smoking
Spirometry
Steroids
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Title Bronchodilator response and lung function decline: Associations with exhaled nitric oxide with regard to sex and smoking status
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