Duration of postviral airway hyperresponsiveness in children with asthma: Effect of atopy
Respiratory viruses induce asthma exacerbations and airway hyperresponsiveness (AHR). Atopy is an important risk factor for asthma persistence. We sought to evaluate whether atopy is a risk factor for prolonged AHR after upper respiratory tract infections (URIs). Twenty-five children (13 atopic and...
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description | Respiratory viruses induce asthma exacerbations and airway hyperresponsiveness (AHR). Atopy is an important risk factor for asthma persistence.
We sought to evaluate whether atopy is a risk factor for prolonged AHR after upper respiratory tract infections (URIs).
Twenty-five children (13 atopic and 12 nonatopic children) with intermittent virus-induced asthma were studied. Clinical evaluation, skin prick tests, methacholine bronchoprovocation, questionnaires, and a nasal wash specimen were obtained at baseline. For 9 months, subjects completed diary cards with respiratory symptoms. During their first reported cold, a nasal wash specimen was obtained. Methacholine provocation was performed 10 days and 5, 7, 9, and 11 weeks later. In case a new cold developed, the provocation schedule was followed from the beginning.
Viruses were detected in 17 (68%) of 25 patients during their first cold, with rhinovirus being most commonly identified (82%). AHR increased significantly 10 days after the URI, equally in both groups (
P
=
.67), and remained so up to the fifth week. Duration of AHR in subjects experiencing a single URI ranged from 5 to 11 weeks, without a significant difference between groups. In the duration of the study, atopic children experienced more colds and asthma exacerbations than nonatopic children. Thus for duration of AHR, significant prolongation was noted in the atopic group when assessed cumulatively.
In asthmatic children the duration of AHR after a single natural cold is 5 to 11 weeks. However, an increased rate of symptomatic cold and asthma episodes in atopic children is associated with considerable cumulative prolongation of AHR, which might help explain the role of atopy as a risk factor for asthma persistence. |
doi_str_mv | 10.1016/j.jaci.2005.04.007 |
format | Article |
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We sought to evaluate whether atopy is a risk factor for prolonged AHR after upper respiratory tract infections (URIs).
Twenty-five children (13 atopic and 12 nonatopic children) with intermittent virus-induced asthma were studied. Clinical evaluation, skin prick tests, methacholine bronchoprovocation, questionnaires, and a nasal wash specimen were obtained at baseline. For 9 months, subjects completed diary cards with respiratory symptoms. During their first reported cold, a nasal wash specimen was obtained. Methacholine provocation was performed 10 days and 5, 7, 9, and 11 weeks later. In case a new cold developed, the provocation schedule was followed from the beginning.
Viruses were detected in 17 (68%) of 25 patients during their first cold, with rhinovirus being most commonly identified (82%). AHR increased significantly 10 days after the URI, equally in both groups (
P
=
.67), and remained so up to the fifth week. Duration of AHR in subjects experiencing a single URI ranged from 5 to 11 weeks, without a significant difference between groups. In the duration of the study, atopic children experienced more colds and asthma exacerbations than nonatopic children. Thus for duration of AHR, significant prolongation was noted in the atopic group when assessed cumulatively.
In asthmatic children the duration of AHR after a single natural cold is 5 to 11 weeks. However, an increased rate of symptomatic cold and asthma episodes in atopic children is associated with considerable cumulative prolongation of AHR, which might help explain the role of atopy as a risk factor for asthma persistence.</description><identifier>ISSN: 0091-6749</identifier><identifier>EISSN: 1097-6825</identifier><identifier>DOI: 10.1016/j.jaci.2005.04.007</identifier><identifier>PMID: 16083783</identifier><identifier>CODEN: JACIBY</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>airway hyperresponsiveness ; Airway management ; Asthma ; Asthma - complications ; atopy ; Biological and medical sciences ; Bronchial Hyperreactivity - etiology ; Case-Control Studies ; Child ; Colds ; Common Cold - complications ; Female ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Humans ; Hypersensitivity - complications ; Immunopathology ; Male ; Medical sciences ; Polymerase Chain Reaction ; Prospective Studies ; Respiratory Tract Infections - complications ; Risk factors ; Secondary education ; Time Factors ; Values ; Variables ; Viral infections ; Virus Diseases - complications ; Virus Diseases - diagnosis ; Viruses ; Viruses - isolation & purification ; Winter</subject><ispartof>Journal of allergy and clinical immunology, 2005-08, Vol.116 (2), p.299-304</ispartof><rights>2005 American Academy of Allergy, Asthma and Immunology</rights><rights>2005 INIST-CNRS</rights><rights>Copyright Elsevier Limited Aug 2005</rights><rights>Copyright © 2005 American Academy of Allergy, Asthma and Immunology. Published by Mosby, Inc. All rights reserved. 2005 American Academy of Allergy, Asthma and Immunology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-254006be1d1ff3ae25b375c0cf7ae55733e3ccd130ea25a3edd35be9702583b23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S009167490500713X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17154548$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16083783$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xepapadaki, Paraskevi</creatorcontrib><creatorcontrib>Papadopoulos, Nikolaos G.</creatorcontrib><creatorcontrib>Bossios, Apostolos</creatorcontrib><creatorcontrib>Manoussakis, Emmanuel</creatorcontrib><creatorcontrib>Manousakas, Theodoros</creatorcontrib><creatorcontrib>Saxoni-Papageorgiou, Photini</creatorcontrib><title>Duration of postviral airway hyperresponsiveness in children with asthma: Effect of atopy</title><title>Journal of allergy and clinical immunology</title><addtitle>J Allergy Clin Immunol</addtitle><description>Respiratory viruses induce asthma exacerbations and airway hyperresponsiveness (AHR). Atopy is an important risk factor for asthma persistence.
We sought to evaluate whether atopy is a risk factor for prolonged AHR after upper respiratory tract infections (URIs).
Twenty-five children (13 atopic and 12 nonatopic children) with intermittent virus-induced asthma were studied. Clinical evaluation, skin prick tests, methacholine bronchoprovocation, questionnaires, and a nasal wash specimen were obtained at baseline. For 9 months, subjects completed diary cards with respiratory symptoms. During their first reported cold, a nasal wash specimen was obtained. Methacholine provocation was performed 10 days and 5, 7, 9, and 11 weeks later. In case a new cold developed, the provocation schedule was followed from the beginning.
Viruses were detected in 17 (68%) of 25 patients during their first cold, with rhinovirus being most commonly identified (82%). AHR increased significantly 10 days after the URI, equally in both groups (
P
=
.67), and remained so up to the fifth week. Duration of AHR in subjects experiencing a single URI ranged from 5 to 11 weeks, without a significant difference between groups. In the duration of the study, atopic children experienced more colds and asthma exacerbations than nonatopic children. Thus for duration of AHR, significant prolongation was noted in the atopic group when assessed cumulatively.
In asthmatic children the duration of AHR after a single natural cold is 5 to 11 weeks. However, an increased rate of symptomatic cold and asthma episodes in atopic children is associated with considerable cumulative prolongation of AHR, which might help explain the role of atopy as a risk factor for asthma persistence.</description><subject>airway hyperresponsiveness</subject><subject>Airway management</subject><subject>Asthma</subject><subject>Asthma - complications</subject><subject>atopy</subject><subject>Biological and medical sciences</subject><subject>Bronchial Hyperreactivity - etiology</subject><subject>Case-Control Studies</subject><subject>Child</subject><subject>Colds</subject><subject>Common Cold - complications</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Humans</subject><subject>Hypersensitivity - complications</subject><subject>Immunopathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Polymerase Chain Reaction</subject><subject>Prospective Studies</subject><subject>Respiratory Tract Infections - complications</subject><subject>Risk factors</subject><subject>Secondary education</subject><subject>Time Factors</subject><subject>Values</subject><subject>Variables</subject><subject>Viral infections</subject><subject>Virus Diseases - complications</subject><subject>Virus Diseases - diagnosis</subject><subject>Viruses</subject><subject>Viruses - isolation & purification</subject><subject>Winter</subject><issn>0091-6749</issn><issn>1097-6825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU2L1TAUhosoznX0D7iQguiu9eSraUUEGccPGHCjC1chTU9tSm9Sk_YO99-bci-OunAVQp7z5pzzZNlTAiUBUr0ay1EbW1IAUQIvAeS9bEegkUVVU3E_2wE0pKgkby6yRzGOkO6sbh5mF6SCmsma7bLv79egF-td7vt89nE52KCnXNtwq4_5cJwxBIyzd9Ee0GGMuXW5GezUBXT5rV2GXMdl2OvX-XXfo1m2HL34-fg4e9DrKeKT83mZfftw_fXqU3Hz5ePnq3c3hRGELAUVHKBqkXSk75lGKlomhQHTS41CSMaQGdMRBqip0Ay7jokWGwlU1Kyl7DJ7e8qd13aPnUG3pAnUHOxeh6Py2qq_X5wd1A9_UJJISmueAl6eA4L_uWJc1N5Gg9OkHfo1qqrmQnDOEvj8H3D0a3BpOEUEcEmbmtSJoifKBB9jwP53KwTU5k2NavOmNm8KuEreUtGzP4e4KzmLSsCLM6Cj0VMftDM23nGSCC749vubE4dp5QeLQUVj0RnsbEh2VOft__r4BVvtuCg</recordid><startdate>20050801</startdate><enddate>20050801</enddate><creator>Xepapadaki, Paraskevi</creator><creator>Papadopoulos, Nikolaos G.</creator><creator>Bossios, Apostolos</creator><creator>Manoussakis, Emmanuel</creator><creator>Manousakas, Theodoros</creator><creator>Saxoni-Papageorgiou, Photini</creator><general>Mosby, Inc</general><general>Elsevier</general><general>Elsevier Limited</general><general>American Academy of Allergy, Asthma and Immunology. Published by Mosby, Inc</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><scope>5PM</scope></search><sort><creationdate>20050801</creationdate><title>Duration of postviral airway hyperresponsiveness in children with asthma: Effect of atopy</title><author>Xepapadaki, Paraskevi ; Papadopoulos, Nikolaos G. ; Bossios, Apostolos ; Manoussakis, Emmanuel ; Manousakas, Theodoros ; Saxoni-Papageorgiou, Photini</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c511t-254006be1d1ff3ae25b375c0cf7ae55733e3ccd130ea25a3edd35be9702583b23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>airway hyperresponsiveness</topic><topic>Airway management</topic><topic>Asthma</topic><topic>Asthma - complications</topic><topic>atopy</topic><topic>Biological and medical sciences</topic><topic>Bronchial Hyperreactivity - etiology</topic><topic>Case-Control Studies</topic><topic>Child</topic><topic>Colds</topic><topic>Common Cold - complications</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Humans</topic><topic>Hypersensitivity - complications</topic><topic>Immunopathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Polymerase Chain Reaction</topic><topic>Prospective Studies</topic><topic>Respiratory Tract Infections - complications</topic><topic>Risk factors</topic><topic>Secondary education</topic><topic>Time Factors</topic><topic>Values</topic><topic>Variables</topic><topic>Viral infections</topic><topic>Virus Diseases - complications</topic><topic>Virus Diseases - diagnosis</topic><topic>Viruses</topic><topic>Viruses - isolation & purification</topic><topic>Winter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xepapadaki, Paraskevi</creatorcontrib><creatorcontrib>Papadopoulos, Nikolaos G.</creatorcontrib><creatorcontrib>Bossios, Apostolos</creatorcontrib><creatorcontrib>Manoussakis, Emmanuel</creatorcontrib><creatorcontrib>Manousakas, Theodoros</creatorcontrib><creatorcontrib>Saxoni-Papageorgiou, Photini</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of allergy and clinical immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xepapadaki, Paraskevi</au><au>Papadopoulos, Nikolaos G.</au><au>Bossios, Apostolos</au><au>Manoussakis, Emmanuel</au><au>Manousakas, Theodoros</au><au>Saxoni-Papageorgiou, Photini</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Duration of postviral airway hyperresponsiveness in children with asthma: Effect of atopy</atitle><jtitle>Journal of allergy and clinical immunology</jtitle><addtitle>J Allergy Clin Immunol</addtitle><date>2005-08-01</date><risdate>2005</risdate><volume>116</volume><issue>2</issue><spage>299</spage><epage>304</epage><pages>299-304</pages><issn>0091-6749</issn><eissn>1097-6825</eissn><coden>JACIBY</coden><abstract>Respiratory viruses induce asthma exacerbations and airway hyperresponsiveness (AHR). Atopy is an important risk factor for asthma persistence.
We sought to evaluate whether atopy is a risk factor for prolonged AHR after upper respiratory tract infections (URIs).
Twenty-five children (13 atopic and 12 nonatopic children) with intermittent virus-induced asthma were studied. Clinical evaluation, skin prick tests, methacholine bronchoprovocation, questionnaires, and a nasal wash specimen were obtained at baseline. For 9 months, subjects completed diary cards with respiratory symptoms. During their first reported cold, a nasal wash specimen was obtained. Methacholine provocation was performed 10 days and 5, 7, 9, and 11 weeks later. In case a new cold developed, the provocation schedule was followed from the beginning.
Viruses were detected in 17 (68%) of 25 patients during their first cold, with rhinovirus being most commonly identified (82%). AHR increased significantly 10 days after the URI, equally in both groups (
P
=
.67), and remained so up to the fifth week. Duration of AHR in subjects experiencing a single URI ranged from 5 to 11 weeks, without a significant difference between groups. In the duration of the study, atopic children experienced more colds and asthma exacerbations than nonatopic children. Thus for duration of AHR, significant prolongation was noted in the atopic group when assessed cumulatively.
In asthmatic children the duration of AHR after a single natural cold is 5 to 11 weeks. However, an increased rate of symptomatic cold and asthma episodes in atopic children is associated with considerable cumulative prolongation of AHR, which might help explain the role of atopy as a risk factor for asthma persistence.</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>16083783</pmid><doi>10.1016/j.jaci.2005.04.007</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | airway hyperresponsiveness Airway management Asthma Asthma - complications atopy Biological and medical sciences Bronchial Hyperreactivity - etiology Case-Control Studies Child Colds Common Cold - complications Female Fundamental and applied biological sciences. Psychology Fundamental immunology Humans Hypersensitivity - complications Immunopathology Male Medical sciences Polymerase Chain Reaction Prospective Studies Respiratory Tract Infections - complications Risk factors Secondary education Time Factors Values Variables Viral infections Virus Diseases - complications Virus Diseases - diagnosis Viruses Viruses - isolation & purification Winter |
title | Duration of postviral airway hyperresponsiveness in children with asthma: Effect of atopy |
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