TY - JOUR
T1 - Functional phenotypes determined by fluctuation-based clustering of lung function measurements in healthy and asthmatic cohort participants
AU - PASTURE Study groups
AU - BIOAIR Study groups
AU - Delgado-Eckert, Edgar
AU - Fuchs, Oliver
AU - Kumar, Nitin
AU - Pekkanen, Juha
AU - Dalphin, Jean Charles
AU - Riedler, Josef
AU - Lauener, Roger
AU - Kabesch, Michael
AU - Kupczyk, Maciej
AU - Dahlen, Sven Erik
AU - Mutius, Erika Von
AU - Frey, Urs
AU - Hyvärinen, Anne
AU - Remes, Sami
AU - Roponen, Marjut
AU - Tiittanen, Pekka
AU - Dalphin, Marie Laure
AU - Kaulek, Vincent
AU - Büchele, Gisela
AU - Depner, Martin
AU - Ege, Markus
AU - Pfefferle, Petra
AU - Renz, Harald
AU - Schaub, Bianca
AU - Bitter, Sondhja
AU - Freil, Remo
AU - Loss, Georg
AU - Roduiti, Caroline
AU - Doeckes, Gert
N1 - Funding Information:
Funding the PaStUre/eFraiM study was supported by the european commission research grants QlK4-ct-2001-00250, FOOD-ct-2006-31708 and KBBe-2007-2-2-06. OF (PaStUre/eFraiM study) is the recipient of a long-term research Fellowship by the european respiratory Society (no. 675) and a training scholarship by the austrian, german and Swiss Paediatric respiratory Society. the BiOair study was supported by the following Swedish research funding bodies: the Medical research council, the Heart-lung Foundation, the Vårdal Foundation, the Stockholm county council (alF), the Swedish asthma and allergy association, the Swedish Foundation for Strategic research, Konsul th c Berghs Foundation, the Karolinska institutet Scilifelab collaborations on translational medicine (chaMP project), the innovative Medicines initiative project U-BiOPreD (unbiased biomarkers for the prediction of respiratory disease outcomes) and Karolinska institutet.
Publisher Copyright:
© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved.
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2018/2/1
Y1 - 2018/2/1
N2 - Rationale Asthma is characterised by inflammation and reversible airway obstruction. However, these features are not always closely related. Fluctuations of daily lung function contain information on asthma phenotypes, exacerbation risk and response to long-acting β-agonists. Objectives In search of subgroups of asthmatic participants with specific lung functional features, we developed and validated a novel clustering approach to asthma phenotyping, which exploits the information contained within the fluctuating behaviour of twice-daily lung function measurements. Methods Forced expiratory volume during the first second (FEV 1) and peak expiratory flow (PEF) were prospectively measured over 4 weeks in 696 healthy and asthmatic school children (Protection Against Allergy - Study in Rural Environments (PASTURE)/EFRAIM cohort), and over 1 year in 138 asthmatic adults with mild-to-moderate or severe asthma (Pan-European Longitudinal Assessment of Clinical Course and BIOmarkers in Severe Chronic AIRway Disease (BIOAIR) cohort). Using enrichment analysis, we explored whether the method identifies clinically meaningful, distinct clusters of participants with different lung functional fluctuation patterns. Measurements and main results In the PASTURE/EFRAIM dataset, we found four distinct clusters. Two clusters were enriched in children with well-known clinical characteristics of asthma. In cluster 3, children from a farming environment predominated, whereas cluster 4 mainly consisted of healthy controls. About 79% of cluster 3 carried the asthma-risk allele rs7216389 of the 17q21 locus. In the BIOAIR dataset, we found two distinct clusters clearly discriminating between individuals with mild-to-moderate and severe asthma. Conclusions Our method identified dynamic functional asthma and healthy phenotypes, partly independent of atopy and inflammation but related to genetic markers on the 17q21 locus. The method can be used for disease phenotyping and possibly endotyping. It may identify participants with specific functional abnormalities, potentially needing a different therapeutic approach.
AB - Rationale Asthma is characterised by inflammation and reversible airway obstruction. However, these features are not always closely related. Fluctuations of daily lung function contain information on asthma phenotypes, exacerbation risk and response to long-acting β-agonists. Objectives In search of subgroups of asthmatic participants with specific lung functional features, we developed and validated a novel clustering approach to asthma phenotyping, which exploits the information contained within the fluctuating behaviour of twice-daily lung function measurements. Methods Forced expiratory volume during the first second (FEV 1) and peak expiratory flow (PEF) were prospectively measured over 4 weeks in 696 healthy and asthmatic school children (Protection Against Allergy - Study in Rural Environments (PASTURE)/EFRAIM cohort), and over 1 year in 138 asthmatic adults with mild-to-moderate or severe asthma (Pan-European Longitudinal Assessment of Clinical Course and BIOmarkers in Severe Chronic AIRway Disease (BIOAIR) cohort). Using enrichment analysis, we explored whether the method identifies clinically meaningful, distinct clusters of participants with different lung functional fluctuation patterns. Measurements and main results In the PASTURE/EFRAIM dataset, we found four distinct clusters. Two clusters were enriched in children with well-known clinical characteristics of asthma. In cluster 3, children from a farming environment predominated, whereas cluster 4 mainly consisted of healthy controls. About 79% of cluster 3 carried the asthma-risk allele rs7216389 of the 17q21 locus. In the BIOAIR dataset, we found two distinct clusters clearly discriminating between individuals with mild-to-moderate and severe asthma. Conclusions Our method identified dynamic functional asthma and healthy phenotypes, partly independent of atopy and inflammation but related to genetic markers on the 17q21 locus. The method can be used for disease phenotyping and possibly endotyping. It may identify participants with specific functional abnormalities, potentially needing a different therapeutic approach.
UR - http://www.scopus.com/inward/record.url?scp=85048123874&partnerID=8YFLogxK
U2 - 10.1136/thoraxjnl-2016-209919
DO - 10.1136/thoraxjnl-2016-209919
M3 - Journal articles
C2 - 28866644
AN - SCOPUS:85048123874
SN - 0040-6376
VL - 73
SP - 107
EP - 115
JO - Thorax
JF - Thorax
IS - 2
ER -