Publication:
Features of asthma which provide meaningful insights for understanding the disease heterogeneity

dc.contributor.coauthorDeliu, M.
dc.contributor.coauthorYavuz, T.S.
dc.contributor.coauthorSperrin, M.
dc.contributor.coauthorBelgrave, D.
dc.contributor.coauthorSahiner, U.M.
dc.contributor.coauthorSackesen, C.
dc.contributor.coauthorKalayci, O.
dc.contributor.coauthorCustovic, A.
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorSaçkesen, Cansın
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T12:31:09Z
dc.date.issued2017
dc.description.abstractBackground: Data-driven methods such as hierarchical clustering (HC) and principal component analysis (PCA) have been used to identify asthma subtypes, with inconsistent results. ObjectiveTo develop a framework for the discovery of stable and clinically meaningful asthma subtypes. MethodsWe performed HC in a rich data set from 613 asthmatic children, using 45 clinical variables (Model 1), and after PCA dimensionality reduction (Model 2). Clinical experts then identified a set of asthma features/domains which informed clusters in the two analyses. In Model 3, we reclustered the data using these features to ascertain whether this improved the discovery process. ResultsCluster stability was poor in Models 1 and 2. Clinical experts highlighted four asthma features/domains which differentiated the clusters in two models: age of onset, allergic sensitization, severity, and recent exacerbations. In Model 3 (HC using these four features), cluster stability improved substantially. The cluster assignment changed, providing more clinically interpretable results. In a 5-cluster model, we labelled the clusters as: Difficult asthma (n=132); Early-onset mild atopic (n=210); Early-onset mild non-atopic: (n=153); Late-onset (n=105); and Exacerbation-prone asthma (n=13). Multinomial regression demonstrated that lung function was significantly diminished among children with Difficult asthma; blood eosinophilia was a significant feature of Difficult, Early-onset mild atopic, and Late-onset asthma. Children with moderate-to-severe asthma were present in each cluster. Conclusions and clinical relevanceAn integrative approach of blending the data with clinical expert domain knowledge identified four features, which may be informative for ascertaining asthma endotypes. These findings suggest that variables which are key determinants of asthma presence, severity, or control may not be the most informative for determining asthma subtypes. Our results indicate that exacerbation-prone asthma may be a separate asthma endotype and that severe asthma is not a single entity, but an extreme end of the spectrum of several different asthma endotypes.
dc.description.fulltextYES
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue1
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipMRC Health eResearch Centre (HeRC) grant
dc.description.sponsorshipMRC
dc.description.versionPublisher version
dc.description.volume48
dc.identifier.doi10.1111/cea.13014
dc.identifier.eissn1365-2222
dc.identifier.embargoNO
dc.identifier.filenameinventorynoIR01215
dc.identifier.issn0954-7894
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85039169762
dc.identifier.urihttps://doi.org/10.1111/cea.13014
dc.identifier.wos422842700006
dc.keywordsAllergic sensitization
dc.keywordsAsthma
dc.keywordsChildhood
dc.keywordsCluster analysis
dc.keywordsEndotypes
dc.keywordsPhenotypes
dc.keywordsSevere asthma
dc.language.isoeng
dc.publisherWiley
dc.relation.grantnoMR/K006665/1
dc.relation.grantnoMR/M015181/1
dc.relation.ispartofClinical and Experimental Allergy
dc.relation.urihttp://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/2415
dc.subjectAllergy
dc.subjectImmunology
dc.titleFeatures of asthma which provide meaningful insights for understanding the disease heterogeneity
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorSaçkesen, Cansın
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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