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Lung function trajectories from birth through puberty reflect atopic disease phenotypes

Karin C. Lødrup Carlsen, Vegard Hovland, Petter Mowinckel, Geir Håland, Kai-Håkon Carlsen
European Respiratory Journal 2013 42: 3018; DOI:
Karin C. Lødrup Carlsen
1Department of Paediatrics, Oslo University Hospital, Oslo, Norway
2Department of Paediatrics, University of Oslo, Oslo, Norway
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Vegard Hovland
1Department of Paediatrics, Oslo University Hospital, Oslo, Norway
2Department of Paediatrics, University of Oslo, Oslo, Norway
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Petter Mowinckel
1Department of Paediatrics, Oslo University Hospital, Oslo, Norway
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Geir Håland
1Department of Paediatrics, Oslo University Hospital, Oslo, Norway
2Department of Paediatrics, University of Oslo, Oslo, Norway
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Kai-Håkon Carlsen
1Department of Paediatrics, Oslo University Hospital, Oslo, Norway
2Department of Paediatrics, University of Oslo, Oslo, Norway
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Abstract

Background: Asthma heterogeneity challenges identification of scientifically and clinically meaningful childhood asthma phenotypes. We asked if lung function trajectories from birth to 16 years reflected time-based (TBP) or atopic-disease (ADP) phenotypes.

Methods: Lung function (z-scores) was measured in the “Environment and Childhood Asthma” birth cohort study in Oslo by tidal flow-volume ratios (time to peak expiratory flow by total expiratory time (tPTEF/tE)) in awake neonates (mean age 2 days) and by forced expiratory flow-volume loops at 10 and 16 years. Data from the 0-2, 10 and 16-years investigations were used to classify all 550 children (52% boys) by recurrent (≥2) bronchial obstruction (rBO) 0-2 years, or asthma (≥2 of doctor diagnosis, asthma symptoms or –medication use) from 2-10 and 10-16 years for the TBP and rBO/asthma with atopic dermatitis and/or allergic rhinitis from 10-16 years as ADP.

Results: Compared to children without asthma 10-16 years, the lung function trajectory for the phenotype asthma, AD and AR from 10-16 years, but not for TCP (figure 1) was significantly reduced from birth (p<0.02) through 10 years by mid-flow values (p< 0.001) and FEV1/FVC (p=0.002), and by FEV1 and mid-flow values (p<0.001) and FEV1/FVC (p<0.04) at 16 years.

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Conclusions: Persistently reduced lung function through childhood was reflected in atopic disease- but not time of symptom presentation based phenotypes.

  • Asthma - diagnosis
  • Lung growth/development
  • Allergy
  • © 2013 ERS
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Lung function trajectories from birth through puberty reflect atopic disease phenotypes
Karin C. Lødrup Carlsen, Vegard Hovland, Petter Mowinckel, Geir Håland, Kai-Håkon Carlsen
European Respiratory Journal Sep 2013, 42 (Suppl 57) 3018;

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Lung function trajectories from birth through puberty reflect atopic disease phenotypes
Karin C. Lødrup Carlsen, Vegard Hovland, Petter Mowinckel, Geir Håland, Kai-Håkon Carlsen
European Respiratory Journal Sep 2013, 42 (Suppl 57) 3018;
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More in this TOC Section

  • Asthma phenotypes in children: Allergic versus non allergic
  • Analysis of risk factors in children with asthma exacerbations treated at the National Institute of Respiratory Diseases "Ismael Cosio Villegas" (INER)
  • Defining uncontrolled childhood asthma in the global PiCA consortium
Show more 7.2 Paediatric Asthma and Allergy

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