Heterogeneity of severe asthma in childhood: Confirmation by cluster analysis of children in the National Institutes of Health/National Heart, Lung, and Blood Institute Severe Asthma Research Program

Background Asthma in children is a heterogeneous disorder with many phenotypes. Although unsupervised cluster analysis is a useful tool for identifying phenotypes, it has not been applied to school-age children with persistent asthma across a wide range of severities. Objectives This study determine...

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Veröffentlicht in:Journal of allergy and clinical immunology 2011-02, Vol.127 (2), p.382-389.e13
Hauptverfasser: Fitzpatrick, Anne M., PhD, Teague, W. Gerald, MD, Meyers, Deborah A., PhD, Peters, Stephen P., MD, PhD, Li, Xingnan, PhD, Li, Huashi, MS, Wenzel, Sally E., MD, Aujla, Shean, MD, Castro, Mario, MD, Bacharier, Leonard B., MD, Gaston, Benjamin M., MD, Bleecker, Eugene R., MD, Moore, Wendy C., MD
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container_end_page 389.e13
container_issue 2
container_start_page 382
container_title Journal of allergy and clinical immunology
container_volume 127
creator Fitzpatrick, Anne M., PhD
Teague, W. Gerald, MD
Meyers, Deborah A., PhD
Peters, Stephen P., MD, PhD
Li, Xingnan, PhD
Li, Huashi, MS
Wenzel, Sally E., MD
Aujla, Shean, MD
Castro, Mario, MD
Bacharier, Leonard B., MD
Gaston, Benjamin M., MD
Bleecker, Eugene R., MD
Moore, Wendy C., MD
description Background Asthma in children is a heterogeneous disorder with many phenotypes. Although unsupervised cluster analysis is a useful tool for identifying phenotypes, it has not been applied to school-age children with persistent asthma across a wide range of severities. Objectives This study determined how children with severe asthma are distributed across a cluster analysis and how well these clusters conform to current definitions of asthma severity. Methods Cluster analysis was applied to 12 continuous and composite variables from 161 children at 5 centers enrolled in the Severe Asthma Research Program. Results Four clusters of asthma were identified. Children in cluster 1 (n = 48) had relatively normal lung function and less atopy. Children in cluster 2 (n = 52) had slightly lower lung function, more atopy, and increased symptoms and medication use. Cluster 3 (n = 32) had greater comorbidity, increased bronchial responsiveness, and lower lung function. Cluster 4 (n = 29) had the lowest lung function and the greatest symptoms and medication use. Predictors of cluster assignment were asthma duration, the number of asthma controller medications, and baseline lung function. Children with severe asthma were present in all clusters, and no cluster corresponded to definitions of asthma severity provided in asthma treatment guidelines. Conclusion Severe asthma in children is highly heterogeneous. Unique phenotypic clusters previously identified in adults can also be identified in children, but with important differences. Larger validation and longitudinal studies are needed to determine the baseline and predictive validity of these phenotypic clusters in the larger clinical setting.
doi_str_mv 10.1016/j.jaci.2010.11.015
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Gerald, MD ; Meyers, Deborah A., PhD ; Peters, Stephen P., MD, PhD ; Li, Xingnan, PhD ; Li, Huashi, MS ; Wenzel, Sally E., MD ; Aujla, Shean, MD ; Castro, Mario, MD ; Bacharier, Leonard B., MD ; Gaston, Benjamin M., MD ; Bleecker, Eugene R., MD ; Moore, Wendy C., MD</creator><creatorcontrib>Fitzpatrick, Anne M., PhD ; Teague, W. Gerald, MD ; Meyers, Deborah A., PhD ; Peters, Stephen P., MD, PhD ; Li, Xingnan, PhD ; Li, Huashi, MS ; Wenzel, Sally E., MD ; Aujla, Shean, MD ; Castro, Mario, MD ; Bacharier, Leonard B., MD ; Gaston, Benjamin M., MD ; Bleecker, Eugene R., MD ; Moore, Wendy C., MD ; National Institutes of Health/National Heart, Lung, and Blood Institute Severe Asthma Research Program</creatorcontrib><description>Background Asthma in children is a heterogeneous disorder with many phenotypes. Although unsupervised cluster analysis is a useful tool for identifying phenotypes, it has not been applied to school-age children with persistent asthma across a wide range of severities. Objectives This study determined how children with severe asthma are distributed across a cluster analysis and how well these clusters conform to current definitions of asthma severity. Methods Cluster analysis was applied to 12 continuous and composite variables from 161 children at 5 centers enrolled in the Severe Asthma Research Program. Results Four clusters of asthma were identified. Children in cluster 1 (n = 48) had relatively normal lung function and less atopy. Children in cluster 2 (n = 52) had slightly lower lung function, more atopy, and increased symptoms and medication use. Cluster 3 (n = 32) had greater comorbidity, increased bronchial responsiveness, and lower lung function. Cluster 4 (n = 29) had the lowest lung function and the greatest symptoms and medication use. Predictors of cluster assignment were asthma duration, the number of asthma controller medications, and baseline lung function. Children with severe asthma were present in all clusters, and no cluster corresponded to definitions of asthma severity provided in asthma treatment guidelines. Conclusion Severe asthma in children is highly heterogeneous. Unique phenotypic clusters previously identified in adults can also be identified in children, but with important differences. Larger validation and longitudinal studies are needed to determine the baseline and predictive validity of these phenotypic clusters in the larger clinical setting.</description><identifier>ISSN: 0091-6749</identifier><identifier>EISSN: 1097-6825</identifier><identifier>DOI: 10.1016/j.jaci.2010.11.015</identifier><identifier>PMID: 21195471</identifier><identifier>CODEN: JACIBY</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>Adolescent ; Age ; Allergic sensitization ; Allergy and Immunology ; Asthma ; Asthma - drug therapy ; Asthma - physiopathology ; asthma guidelines ; Biological and medical sciences ; Blood ; Child ; children ; Cluster Analysis ; Female ; Forced Expiratory Volume ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Humans ; Immunopathology ; Lung - physiopathology ; lung function ; Male ; Medical sciences ; National Institutes of Health (U.S.) ; Pediatrics ; phenotype ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; severe asthma ; United States ; Variables</subject><ispartof>Journal of allergy and clinical immunology, 2011-02, Vol.127 (2), p.382-389.e13</ispartof><rights>American Academy of Allergy, Asthma &amp; Immunology</rights><rights>2011 American Academy of Allergy, Asthma &amp; Immunology</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 American Academy of Allergy, Asthma &amp; Immunology. Published by Mosby, Inc. 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Gerald, MD</creatorcontrib><creatorcontrib>Meyers, Deborah A., PhD</creatorcontrib><creatorcontrib>Peters, Stephen P., MD, PhD</creatorcontrib><creatorcontrib>Li, Xingnan, PhD</creatorcontrib><creatorcontrib>Li, Huashi, MS</creatorcontrib><creatorcontrib>Wenzel, Sally E., MD</creatorcontrib><creatorcontrib>Aujla, Shean, MD</creatorcontrib><creatorcontrib>Castro, Mario, MD</creatorcontrib><creatorcontrib>Bacharier, Leonard B., MD</creatorcontrib><creatorcontrib>Gaston, Benjamin M., MD</creatorcontrib><creatorcontrib>Bleecker, Eugene R., MD</creatorcontrib><creatorcontrib>Moore, Wendy C., MD</creatorcontrib><creatorcontrib>National Institutes of Health/National Heart, Lung, and Blood Institute Severe Asthma Research Program</creatorcontrib><title>Heterogeneity of severe asthma in childhood: Confirmation by cluster analysis of children in the National Institutes of Health/National Heart, Lung, and Blood Institute Severe Asthma Research Program</title><title>Journal of allergy and clinical immunology</title><addtitle>J Allergy Clin Immunol</addtitle><description>Background Asthma in children is a heterogeneous disorder with many phenotypes. Although unsupervised cluster analysis is a useful tool for identifying phenotypes, it has not been applied to school-age children with persistent asthma across a wide range of severities. Objectives This study determined how children with severe asthma are distributed across a cluster analysis and how well these clusters conform to current definitions of asthma severity. Methods Cluster analysis was applied to 12 continuous and composite variables from 161 children at 5 centers enrolled in the Severe Asthma Research Program. Results Four clusters of asthma were identified. Children in cluster 1 (n = 48) had relatively normal lung function and less atopy. Children in cluster 2 (n = 52) had slightly lower lung function, more atopy, and increased symptoms and medication use. Cluster 3 (n = 32) had greater comorbidity, increased bronchial responsiveness, and lower lung function. Cluster 4 (n = 29) had the lowest lung function and the greatest symptoms and medication use. Predictors of cluster assignment were asthma duration, the number of asthma controller medications, and baseline lung function. Children with severe asthma were present in all clusters, and no cluster corresponded to definitions of asthma severity provided in asthma treatment guidelines. Conclusion Severe asthma in children is highly heterogeneous. Unique phenotypic clusters previously identified in adults can also be identified in children, but with important differences. Larger validation and longitudinal studies are needed to determine the baseline and predictive validity of these phenotypic clusters in the larger clinical setting.</description><subject>Adolescent</subject><subject>Age</subject><subject>Allergic sensitization</subject><subject>Allergy and Immunology</subject><subject>Asthma</subject><subject>Asthma - drug therapy</subject><subject>Asthma - physiopathology</subject><subject>asthma guidelines</subject><subject>Biological and medical sciences</subject><subject>Blood</subject><subject>Child</subject><subject>children</subject><subject>Cluster Analysis</subject><subject>Female</subject><subject>Forced Expiratory Volume</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Humans</subject><subject>Immunopathology</subject><subject>Lung - physiopathology</subject><subject>lung function</subject><subject>Male</subject><subject>Medical sciences</subject><subject>National Institutes of Health (U.S.)</subject><subject>Pediatrics</subject><subject>phenotype</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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Gerald, MD ; Meyers, Deborah A., PhD ; Peters, Stephen P., MD, PhD ; Li, Xingnan, PhD ; Li, Huashi, MS ; Wenzel, Sally E., MD ; Aujla, Shean, MD ; Castro, Mario, MD ; Bacharier, Leonard B., MD ; Gaston, Benjamin M., MD ; Bleecker, Eugene R., MD ; Moore, Wendy C., MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c578t-d958b67e33452207fa6cef7aa2106f5bef9dbe990d02e58ef8be6947069aaefb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adolescent</topic><topic>Age</topic><topic>Allergic sensitization</topic><topic>Allergy and Immunology</topic><topic>Asthma</topic><topic>Asthma - drug therapy</topic><topic>Asthma - physiopathology</topic><topic>asthma guidelines</topic><topic>Biological and medical sciences</topic><topic>Blood</topic><topic>Child</topic><topic>children</topic><topic>Cluster Analysis</topic><topic>Female</topic><topic>Forced Expiratory Volume</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Humans</topic><topic>Immunopathology</topic><topic>Lung - physiopathology</topic><topic>lung function</topic><topic>Male</topic><topic>Medical sciences</topic><topic>National Institutes of Health (U.S.)</topic><topic>Pediatrics</topic><topic>phenotype</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>severe asthma</topic><topic>United States</topic><topic>Variables</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fitzpatrick, Anne M., PhD</creatorcontrib><creatorcontrib>Teague, W. Gerald, MD</creatorcontrib><creatorcontrib>Meyers, Deborah A., PhD</creatorcontrib><creatorcontrib>Peters, Stephen P., MD, PhD</creatorcontrib><creatorcontrib>Li, Xingnan, PhD</creatorcontrib><creatorcontrib>Li, Huashi, MS</creatorcontrib><creatorcontrib>Wenzel, Sally E., MD</creatorcontrib><creatorcontrib>Aujla, Shean, MD</creatorcontrib><creatorcontrib>Castro, Mario, MD</creatorcontrib><creatorcontrib>Bacharier, Leonard B., MD</creatorcontrib><creatorcontrib>Gaston, Benjamin M., MD</creatorcontrib><creatorcontrib>Bleecker, Eugene R., MD</creatorcontrib><creatorcontrib>Moore, Wendy C., MD</creatorcontrib><creatorcontrib>National Institutes of Health/National Heart, Lung, and Blood Institute Severe Asthma Research Program</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of allergy and clinical immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fitzpatrick, Anne M., PhD</au><au>Teague, W. Gerald, MD</au><au>Meyers, Deborah A., PhD</au><au>Peters, Stephen P., MD, PhD</au><au>Li, Xingnan, PhD</au><au>Li, Huashi, MS</au><au>Wenzel, Sally E., MD</au><au>Aujla, Shean, MD</au><au>Castro, Mario, MD</au><au>Bacharier, Leonard B., MD</au><au>Gaston, Benjamin M., MD</au><au>Bleecker, Eugene R., MD</au><au>Moore, Wendy C., MD</au><aucorp>National Institutes of Health/National Heart, Lung, and Blood Institute Severe Asthma Research Program</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Heterogeneity of severe asthma in childhood: Confirmation by cluster analysis of children in the National Institutes of Health/National Heart, Lung, and Blood Institute Severe Asthma Research Program</atitle><jtitle>Journal of allergy and clinical immunology</jtitle><addtitle>J Allergy Clin Immunol</addtitle><date>2011-02-01</date><risdate>2011</risdate><volume>127</volume><issue>2</issue><spage>382</spage><epage>389.e13</epage><pages>382-389.e13</pages><issn>0091-6749</issn><eissn>1097-6825</eissn><coden>JACIBY</coden><abstract>Background Asthma in children is a heterogeneous disorder with many phenotypes. Although unsupervised cluster analysis is a useful tool for identifying phenotypes, it has not been applied to school-age children with persistent asthma across a wide range of severities. Objectives This study determined how children with severe asthma are distributed across a cluster analysis and how well these clusters conform to current definitions of asthma severity. Methods Cluster analysis was applied to 12 continuous and composite variables from 161 children at 5 centers enrolled in the Severe Asthma Research Program. Results Four clusters of asthma were identified. Children in cluster 1 (n = 48) had relatively normal lung function and less atopy. Children in cluster 2 (n = 52) had slightly lower lung function, more atopy, and increased symptoms and medication use. Cluster 3 (n = 32) had greater comorbidity, increased bronchial responsiveness, and lower lung function. Cluster 4 (n = 29) had the lowest lung function and the greatest symptoms and medication use. Predictors of cluster assignment were asthma duration, the number of asthma controller medications, and baseline lung function. Children with severe asthma were present in all clusters, and no cluster corresponded to definitions of asthma severity provided in asthma treatment guidelines. Conclusion Severe asthma in children is highly heterogeneous. Unique phenotypic clusters previously identified in adults can also be identified in children, but with important differences. Larger validation and longitudinal studies are needed to determine the baseline and predictive validity of these phenotypic clusters in the larger clinical setting.</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>21195471</pmid><doi>10.1016/j.jaci.2010.11.015</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Age
Allergic sensitization
Allergy and Immunology
Asthma
Asthma - drug therapy
Asthma - physiopathology
asthma guidelines
Biological and medical sciences
Blood
Child
children
Cluster Analysis
Female
Forced Expiratory Volume
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Humans
Immunopathology
Lung - physiopathology
lung function
Male
Medical sciences
National Institutes of Health (U.S.)
Pediatrics
phenotype
Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis
severe asthma
United States
Variables
title Heterogeneity of severe asthma in childhood: Confirmation by cluster analysis of children in the National Institutes of Health/National Heart, Lung, and Blood Institute Severe Asthma Research Program
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