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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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 & Immunology</rights><rights>2011 American Academy of Allergy, Asthma & Immunology</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 American Academy of Allergy, Asthma & Immunology. Published by Mosby, Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Feb 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c578t-d958b67e33452207fa6cef7aa2106f5bef9dbe990d02e58ef8be6947069aaefb3</citedby><cites>FETCH-LOGICAL-c578t-d958b67e33452207fa6cef7aa2106f5bef9dbe990d02e58ef8be6947069aaefb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0091674910017653$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23889740$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21195471$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><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. Vasculitis</subject><subject>severe asthma</subject><subject>United States</subject><subject>Variables</subject><issn>0091-6749</issn><issn>1097-6825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kt9u0zAUxiMEYmXwAlwgSwhxs3Z2Eif2hJBGBXRSBYjBteU4J4uLYw_bmdQn5LVw2rJKu-DKOvbvO_8-Z9lLghcEk-p8s9hIpRc5ni7IAhP6KJsRzOt5xXL6OJthzMm8qkt-kj0LYYNTXDD-NDvJCeG0rMks-7OCCN7dgAUdt8h1KMAdeEAyxH6QSFukem3a3rn2Ai2d7bQfZNTOomaLlBlDkiNppdkGHSb9DvdgJ2nsAX3Z0dKgKxuijmOEHbYCaWJ_fv-aYh_P0Hq0N2cpX4s-mFTyKELX-74u9319h5AEqkffUvNeDs-zJ500AV4cztPs56ePP5ar-frr56vl5XquaM3ivOWUNVUNRVHSPMd1JysFXS1lTnDV0QY63jbAOW5xDpRBxxqoeFnjiksJXVOcZm_3eW-9-z1CiGLQQYEx0oIbg2AlY2m7uErk6wfkxo0-jRoEoRSTZEXOEpXvKeVdCB46cev1IP1WECwml8VGTC6LyWVBiEguJ9GrQ-qxGaC9l_yzNQFvDoAMSprOS6t0OHIFY7wuceLe7TlIK7vT4EVQGqyCVntQUbRO_7-P9w_kymirU8VfsIVwnFeEXGBxPf3H6TsSjEld0aL4C7ye3eQ</recordid><startdate>20110201</startdate><enddate>20110201</enddate><creator>Fitzpatrick, Anne M., PhD</creator><creator>Teague, W. Gerald, MD</creator><creator>Meyers, Deborah A., PhD</creator><creator>Peters, Stephen P., MD, PhD</creator><creator>Li, Xingnan, PhD</creator><creator>Li, Huashi, MS</creator><creator>Wenzel, Sally E., MD</creator><creator>Aujla, Shean, MD</creator><creator>Castro, Mario, MD</creator><creator>Bacharier, Leonard B., MD</creator><creator>Gaston, Benjamin M., MD</creator><creator>Bleecker, Eugene R., MD</creator><creator>Moore, Wendy C., MD</creator><general>Mosby, Inc</general><general>Elsevier</general><general>Elsevier Limited</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SS</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20110201</creationdate><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><author>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</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 & Medical Complete (Alumni)</collection><collection>Nursing & 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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