Lung function and bronchial hyper‐reactivity from 11 to 18 years in children with bronchiolitis in infancy
Background Various trajectories for lung function and bronchial hyper‐reactivity (BHR) from early childhood to adulthood are described, including puberty as a period with excessive lung growth. Bronchiolitis in infancy may be associated with increased risk of developing chronic obstructive pulmonary...
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Veröffentlicht in: | Pediatric allergy and immunology 2020-01, Vol.31 (1), p.57-65 |
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description | Background
Various trajectories for lung function and bronchial hyper‐reactivity (BHR) from early childhood to adulthood are described, including puberty as a period with excessive lung growth. Bronchiolitis in infancy may be associated with increased risk of developing chronic obstructive pulmonary disease, but the development of respiratory patterns during puberty is poorly characterized for these children. We aimed to study the development and trajectories of lung function and BHR from 11 to 18 years of age in children hospitalized for bronchiolitis in infancy.
Methods
Infants hospitalized for bronchiolitis at the University Hospitals in Stavanger and Bergen, Norway, during 1997‐1998, and an age‐matched control group, were included in a longitudinal follow‐up study and examined at 11 and 18 years of age with spirometry and methacholine provocation test (MPT). The MPT data were managed as dose‐response slope (DRS) in the statistical analyses. Changes in lung function and DRS from 11 to 18 years of age were analyzed by generalized estimating equations, including interaction terms.
Results
z‐scores for forced vital capacity (FVC), forced expiratory volume in first second (FEV1), FEV1/FVC ratio, and DRS were not different from 11 to 18 years of age in both the post‐bronchiolitis and the control group. The trajectories from 11 to 18 years did not differ between the two groups. BHR at age 11 was independently associated with asthma at age 18.
Conclusion
Children hospitalized for bronchiolitis had stable predicted lung function and BHR from 11 to 18 years of age. The lung function trajectories were not different from controls. |
doi_str_mv | 10.1111/pai.13137 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2303201957</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2331911129</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3887-68fc3f034997801ea4d16458342d5537f66c2e39d075101c79d1718b535e8feb3</originalsourceid><addsrcrecordid>eNp1kU9O3DAUh62KqkxpF70AstQNLAJ-cRzbSzQqf6SR6ALWkcexO0aJPdgJKLsegSNwlh6lJ6mZGVhU4m28eJ8_Pf1-CH0DcgJ5TtfKnQAFyj-gGVApC0qo2EMzIgkramB8H31O6Y4Q4LSGT2ifApOMVeUM9YvR_8J29HpwwWPlW7yMweuVUx1eTWsT__5-ikbl9YMbJmxj6DEAHgIG8ed5Miom7DzOH7o2Go8f3bB6VYTODW6zdt4qr6cv6KNVXTJfd-8Buj3_cTO_LBbXF1fzs0WhqRC8qIXV1BJaSckFAaOqFuqKCVqVLWOU27rWpaGyJZwBAc1lCxzEklFmhDVLeoCOtt51DPejSUPTu6RN1ylvwpiaMgdUEpCMZ_T7f-hdGKPP12WKgsz5ljJTx1tKx5BSNLZZR9erODVAmpcOmtxBs-kgs4c747jsTftGvoaegdMt8Og6M71van6eXW2V_wD4PZB6</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2331911129</pqid></control><display><type>article</type><title>Lung function and bronchial hyper‐reactivity from 11 to 18 years in children with bronchiolitis in infancy</title><source>MEDLINE</source><source>Wiley Online Library All Journals</source><creator>Sørensen, Karen Galta ; Øymar, Knut ; Dalen, Ingvild ; Halvorsen, Thomas ; Mikalsen, Ingvild Bruun ; Genuneit, Jon</creator><contributor>Genuneit, Jon</contributor><creatorcontrib>Sørensen, Karen Galta ; Øymar, Knut ; Dalen, Ingvild ; Halvorsen, Thomas ; Mikalsen, Ingvild Bruun ; Genuneit, Jon ; Genuneit, Jon</creatorcontrib><description>Background
Various trajectories for lung function and bronchial hyper‐reactivity (BHR) from early childhood to adulthood are described, including puberty as a period with excessive lung growth. Bronchiolitis in infancy may be associated with increased risk of developing chronic obstructive pulmonary disease, but the development of respiratory patterns during puberty is poorly characterized for these children. We aimed to study the development and trajectories of lung function and BHR from 11 to 18 years of age in children hospitalized for bronchiolitis in infancy.
Methods
Infants hospitalized for bronchiolitis at the University Hospitals in Stavanger and Bergen, Norway, during 1997‐1998, and an age‐matched control group, were included in a longitudinal follow‐up study and examined at 11 and 18 years of age with spirometry and methacholine provocation test (MPT). The MPT data were managed as dose‐response slope (DRS) in the statistical analyses. Changes in lung function and DRS from 11 to 18 years of age were analyzed by generalized estimating equations, including interaction terms.
Results
z‐scores for forced vital capacity (FVC), forced expiratory volume in first second (FEV1), FEV1/FVC ratio, and DRS were not different from 11 to 18 years of age in both the post‐bronchiolitis and the control group. The trajectories from 11 to 18 years did not differ between the two groups. BHR at age 11 was independently associated with asthma at age 18.
Conclusion
Children hospitalized for bronchiolitis had stable predicted lung function and BHR from 11 to 18 years of age. The lung function trajectories were not different from controls.</description><identifier>ISSN: 0905-6157</identifier><identifier>EISSN: 1399-3038</identifier><identifier>DOI: 10.1111/pai.13137</identifier><identifier>PMID: 31595542</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Adolescent ; Age ; Asthma ; Bronchial Hyperreactivity - epidemiology ; bronchial hyper‐reactivity ; bronchial provocation tests ; bronchiolitis ; Bronchiolitis - complications ; Bronchopneumonia ; Child ; Children ; Chronic obstructive pulmonary disease ; Female ; Follow-Up Studies ; Hospitalization ; Humans ; Infant ; Infant, Newborn ; Infants ; Longitudinal Studies ; Lung diseases ; Male ; Methacholine ; methacholine chloride ; Norway ; Obstructive lung disease ; Puberty ; Respiration ; Respiratory function ; Respiratory Function Tests ; spirometry ; Statistical analysis ; Teenagers</subject><ispartof>Pediatric allergy and immunology, 2020-01, Vol.31 (1), p.57-65</ispartof><rights>2019 The Authors. published by John Wiley & Sons Ltd.</rights><rights>2019 The Authors. Pediatric Allergy and Immunology published by John Wiley & Sons Ltd.</rights><rights>Copyright © 2020 John Wiley & Sons A/S</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3887-68fc3f034997801ea4d16458342d5537f66c2e39d075101c79d1718b535e8feb3</citedby><cites>FETCH-LOGICAL-c3887-68fc3f034997801ea4d16458342d5537f66c2e39d075101c79d1718b535e8feb3</cites><orcidid>0000-0001-7530-2933</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fpai.13137$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fpai.13137$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31595542$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Genuneit, Jon</contributor><creatorcontrib>Sørensen, Karen Galta</creatorcontrib><creatorcontrib>Øymar, Knut</creatorcontrib><creatorcontrib>Dalen, Ingvild</creatorcontrib><creatorcontrib>Halvorsen, Thomas</creatorcontrib><creatorcontrib>Mikalsen, Ingvild Bruun</creatorcontrib><creatorcontrib>Genuneit, Jon</creatorcontrib><title>Lung function and bronchial hyper‐reactivity from 11 to 18 years in children with bronchiolitis in infancy</title><title>Pediatric allergy and immunology</title><addtitle>Pediatr Allergy Immunol</addtitle><description>Background
Various trajectories for lung function and bronchial hyper‐reactivity (BHR) from early childhood to adulthood are described, including puberty as a period with excessive lung growth. Bronchiolitis in infancy may be associated with increased risk of developing chronic obstructive pulmonary disease, but the development of respiratory patterns during puberty is poorly characterized for these children. We aimed to study the development and trajectories of lung function and BHR from 11 to 18 years of age in children hospitalized for bronchiolitis in infancy.
Methods
Infants hospitalized for bronchiolitis at the University Hospitals in Stavanger and Bergen, Norway, during 1997‐1998, and an age‐matched control group, were included in a longitudinal follow‐up study and examined at 11 and 18 years of age with spirometry and methacholine provocation test (MPT). The MPT data were managed as dose‐response slope (DRS) in the statistical analyses. Changes in lung function and DRS from 11 to 18 years of age were analyzed by generalized estimating equations, including interaction terms.
Results
z‐scores for forced vital capacity (FVC), forced expiratory volume in first second (FEV1), FEV1/FVC ratio, and DRS were not different from 11 to 18 years of age in both the post‐bronchiolitis and the control group. The trajectories from 11 to 18 years did not differ between the two groups. BHR at age 11 was independently associated with asthma at age 18.
Conclusion
Children hospitalized for bronchiolitis had stable predicted lung function and BHR from 11 to 18 years of age. The lung function trajectories were not different from controls.</description><subject>Adolescent</subject><subject>Age</subject><subject>Asthma</subject><subject>Bronchial Hyperreactivity - epidemiology</subject><subject>bronchial hyper‐reactivity</subject><subject>bronchial provocation tests</subject><subject>bronchiolitis</subject><subject>Bronchiolitis - complications</subject><subject>Bronchopneumonia</subject><subject>Child</subject><subject>Children</subject><subject>Chronic obstructive pulmonary disease</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Hospitalization</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Infants</subject><subject>Longitudinal Studies</subject><subject>Lung diseases</subject><subject>Male</subject><subject>Methacholine</subject><subject>methacholine chloride</subject><subject>Norway</subject><subject>Obstructive lung disease</subject><subject>Puberty</subject><subject>Respiration</subject><subject>Respiratory function</subject><subject>Respiratory Function Tests</subject><subject>spirometry</subject><subject>Statistical analysis</subject><subject>Teenagers</subject><issn>0905-6157</issn><issn>1399-3038</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNp1kU9O3DAUh62KqkxpF70AstQNLAJ-cRzbSzQqf6SR6ALWkcexO0aJPdgJKLsegSNwlh6lJ6mZGVhU4m28eJ8_Pf1-CH0DcgJ5TtfKnQAFyj-gGVApC0qo2EMzIgkramB8H31O6Y4Q4LSGT2ifApOMVeUM9YvR_8J29HpwwWPlW7yMweuVUx1eTWsT__5-ikbl9YMbJmxj6DEAHgIG8ed5Miom7DzOH7o2Go8f3bB6VYTODW6zdt4qr6cv6KNVXTJfd-8Buj3_cTO_LBbXF1fzs0WhqRC8qIXV1BJaSckFAaOqFuqKCVqVLWOU27rWpaGyJZwBAc1lCxzEklFmhDVLeoCOtt51DPejSUPTu6RN1ylvwpiaMgdUEpCMZ_T7f-hdGKPP12WKgsz5ljJTx1tKx5BSNLZZR9erODVAmpcOmtxBs-kgs4c747jsTftGvoaegdMt8Og6M71van6eXW2V_wD4PZB6</recordid><startdate>202001</startdate><enddate>202001</enddate><creator>Sørensen, Karen Galta</creator><creator>Øymar, Knut</creator><creator>Dalen, Ingvild</creator><creator>Halvorsen, Thomas</creator><creator>Mikalsen, Ingvild Bruun</creator><creator>Genuneit, Jon</creator><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>WIN</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>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7530-2933</orcidid></search><sort><creationdate>202001</creationdate><title>Lung function and bronchial hyper‐reactivity from 11 to 18 years in children with bronchiolitis in infancy</title><author>Sørensen, Karen Galta ; Øymar, Knut ; Dalen, Ingvild ; Halvorsen, Thomas ; Mikalsen, Ingvild Bruun ; Genuneit, Jon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3887-68fc3f034997801ea4d16458342d5537f66c2e39d075101c79d1718b535e8feb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adolescent</topic><topic>Age</topic><topic>Asthma</topic><topic>Bronchial Hyperreactivity - epidemiology</topic><topic>bronchial hyper‐reactivity</topic><topic>bronchial provocation tests</topic><topic>bronchiolitis</topic><topic>Bronchiolitis - complications</topic><topic>Bronchopneumonia</topic><topic>Child</topic><topic>Children</topic><topic>Chronic obstructive pulmonary disease</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Hospitalization</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Infants</topic><topic>Longitudinal Studies</topic><topic>Lung diseases</topic><topic>Male</topic><topic>Methacholine</topic><topic>methacholine chloride</topic><topic>Norway</topic><topic>Obstructive lung disease</topic><topic>Puberty</topic><topic>Respiration</topic><topic>Respiratory function</topic><topic>Respiratory Function Tests</topic><topic>spirometry</topic><topic>Statistical analysis</topic><topic>Teenagers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sørensen, Karen Galta</creatorcontrib><creatorcontrib>Øymar, Knut</creatorcontrib><creatorcontrib>Dalen, Ingvild</creatorcontrib><creatorcontrib>Halvorsen, Thomas</creatorcontrib><creatorcontrib>Mikalsen, Ingvild Bruun</creatorcontrib><creatorcontrib>Genuneit, Jon</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</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>Pediatric allergy and immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sørensen, Karen Galta</au><au>Øymar, Knut</au><au>Dalen, Ingvild</au><au>Halvorsen, Thomas</au><au>Mikalsen, Ingvild Bruun</au><au>Genuneit, Jon</au><au>Genuneit, Jon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lung function and bronchial hyper‐reactivity from 11 to 18 years in children with bronchiolitis in infancy</atitle><jtitle>Pediatric allergy and immunology</jtitle><addtitle>Pediatr Allergy Immunol</addtitle><date>2020-01</date><risdate>2020</risdate><volume>31</volume><issue>1</issue><spage>57</spage><epage>65</epage><pages>57-65</pages><issn>0905-6157</issn><eissn>1399-3038</eissn><abstract>Background
Various trajectories for lung function and bronchial hyper‐reactivity (BHR) from early childhood to adulthood are described, including puberty as a period with excessive lung growth. Bronchiolitis in infancy may be associated with increased risk of developing chronic obstructive pulmonary disease, but the development of respiratory patterns during puberty is poorly characterized for these children. We aimed to study the development and trajectories of lung function and BHR from 11 to 18 years of age in children hospitalized for bronchiolitis in infancy.
Methods
Infants hospitalized for bronchiolitis at the University Hospitals in Stavanger and Bergen, Norway, during 1997‐1998, and an age‐matched control group, were included in a longitudinal follow‐up study and examined at 11 and 18 years of age with spirometry and methacholine provocation test (MPT). The MPT data were managed as dose‐response slope (DRS) in the statistical analyses. Changes in lung function and DRS from 11 to 18 years of age were analyzed by generalized estimating equations, including interaction terms.
Results
z‐scores for forced vital capacity (FVC), forced expiratory volume in first second (FEV1), FEV1/FVC ratio, and DRS were not different from 11 to 18 years of age in both the post‐bronchiolitis and the control group. The trajectories from 11 to 18 years did not differ between the two groups. BHR at age 11 was independently associated with asthma at age 18.
Conclusion
Children hospitalized for bronchiolitis had stable predicted lung function and BHR from 11 to 18 years of age. The lung function trajectories were not different from controls.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31595542</pmid><doi>10.1111/pai.13137</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-7530-2933</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Age Asthma Bronchial Hyperreactivity - epidemiology bronchial hyper‐reactivity bronchial provocation tests bronchiolitis Bronchiolitis - complications Bronchopneumonia Child Children Chronic obstructive pulmonary disease Female Follow-Up Studies Hospitalization Humans Infant Infant, Newborn Infants Longitudinal Studies Lung diseases Male Methacholine methacholine chloride Norway Obstructive lung disease Puberty Respiration Respiratory function Respiratory Function Tests spirometry Statistical analysis Teenagers |
title | Lung function and bronchial hyper‐reactivity from 11 to 18 years in children with bronchiolitis in infancy |
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