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Natural history of allergic sensitization in infants with early-onset atopic dermatitis: results from ORCA Study

Background Early‐onset atopic dermatitis (AD) is a particular phenotype that may convey a risk of developing multiple sensitizations to allergens but little is known about the pathway of sensitization. The aims of this study were to describe the natural history of sensitization to allergens for this...

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Published in:Pediatric allergy and immunology 2014-11, Vol.25 (7), p.668-673
Main Authors: Just, Jocelyne, Deslandes-Boutmy, Emmanuelle, Amat, Flore, Desseaux, Kristell, Nemni, Ariane, Bourrat, Emmanuelle, Sahraoui, Fatia, Pansé, Isabelle, Bagot, Martine, Fouéré, Sébastien
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container_title Pediatric allergy and immunology
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creator Just, Jocelyne
Deslandes-Boutmy, Emmanuelle
Amat, Flore
Desseaux, Kristell
Nemni, Ariane
Bourrat, Emmanuelle
Sahraoui, Fatia
Pansé, Isabelle
Bagot, Martine
Fouéré, Sébastien
description Background Early‐onset atopic dermatitis (AD) is a particular phenotype that may convey a risk of developing multiple sensitizations to allergens but little is known about the pathway of sensitization. The aims of this study were to describe the natural history of sensitization to allergens for this phenotype and to identify the most predictive marker associated with the risk of developing sensitization to inhaled allergens in a well‐selected cohort of infants with AD. Methods Infants with active AD were enrolled and prospectively explored for biological markers of atopy every year until the age of 6 yr. Allergic sensitization was defined as the presence of positive specific IgEs to allergens and multiple sensitizations as being sensitized to ≥2 allergens. Elevated blood eosinophilia was defined as an eosinophil blood count ≥470 eosinophils/mm3 and elevated total IgE as a serum IgE level ≥45 kU/l. Results Two hundred and twenty‐nine infants were included. Elevated blood eosinophilia was observed at baseline in 60 children (26.2%) and elevated total IgE in 85 (37.1%). When elevated at baseline, eosinophilia and IgE levels remained significantly higher during the follow‐up period. Sensitization to food allergens decreased from 58% to 34%, whereas sensitization to inhaled allergens increased over time from 17% to 67%. Initial multiple sensitizations to food allergens were the most predictive factor for the risk of developing sensitization to inhaled allergens at 6 yr (OR 3.72 [1.68–8.30] p 
doi_str_mv 10.1111/pai.12287
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The aims of this study were to describe the natural history of sensitization to allergens for this phenotype and to identify the most predictive marker associated with the risk of developing sensitization to inhaled allergens in a well‐selected cohort of infants with AD. Methods Infants with active AD were enrolled and prospectively explored for biological markers of atopy every year until the age of 6 yr. Allergic sensitization was defined as the presence of positive specific IgEs to allergens and multiple sensitizations as being sensitized to ≥2 allergens. Elevated blood eosinophilia was defined as an eosinophil blood count ≥470 eosinophils/mm3 and elevated total IgE as a serum IgE level ≥45 kU/l. Results Two hundred and twenty‐nine infants were included. Elevated blood eosinophilia was observed at baseline in 60 children (26.2%) and elevated total IgE in 85 (37.1%). When elevated at baseline, eosinophilia and IgE levels remained significantly higher during the follow‐up period. Sensitization to food allergens decreased from 58% to 34%, whereas sensitization to inhaled allergens increased over time from 17% to 67%. Initial multiple sensitizations to food allergens were the most predictive factor for the risk of developing sensitization to inhaled allergens at 6 yr (OR 3.72 [1.68–8.30] p &lt; 0.001). Conclusions In the early‐onset AD phenotype, multiple sensitization to food allergens conveys a higher risk of sensitization to inhaled allergens than single sensitization.</description><identifier>ISSN: 0905-6157</identifier><identifier>EISSN: 1399-3038</identifier><identifier>DOI: 10.1111/pai.12287</identifier><identifier>PMID: 25283304</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Age of Onset ; Allergens - adverse effects ; Allergens - immunology ; Allergies ; atopic dermatitis ; Child ; Child, Preschool ; cohort ; Cohort Studies ; Dermatitis ; Dermatitis, Atopic - epidemiology ; Dermatitis, Atopic - immunology ; Eosinophilia - epidemiology ; Eosinophilia - immunology ; Female ; Follow-Up Studies ; Food - adverse effects ; food allergens ; Food Hypersensitivity - epidemiology ; Food Hypersensitivity - immunology ; Genotype &amp; phenotype ; Humans ; Immunization ; Immunoglobulin E - blood ; Infant ; Infant, Newborn ; inhaled allergens ; Male ; Medical History Taking ; Medical treatment ; phenotypes ; Prospective Studies ; sensitization</subject><ispartof>Pediatric allergy and immunology, 2014-11, Vol.25 (7), p.668-673</ispartof><rights>2014 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd</rights><rights>2014 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2014 John Wiley &amp; Sons A/S</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4267-c947a63caf3605fd2264c8795dfff60e4f8ec4bcd27a457918351c373266782c3</citedby><cites>FETCH-LOGICAL-c4267-c947a63caf3605fd2264c8795dfff60e4f8ec4bcd27a457918351c373266782c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25283304$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Just, Jocelyne</creatorcontrib><creatorcontrib>Deslandes-Boutmy, Emmanuelle</creatorcontrib><creatorcontrib>Amat, Flore</creatorcontrib><creatorcontrib>Desseaux, Kristell</creatorcontrib><creatorcontrib>Nemni, Ariane</creatorcontrib><creatorcontrib>Bourrat, Emmanuelle</creatorcontrib><creatorcontrib>Sahraoui, Fatia</creatorcontrib><creatorcontrib>Pansé, Isabelle</creatorcontrib><creatorcontrib>Bagot, Martine</creatorcontrib><creatorcontrib>Fouéré, Sébastien</creatorcontrib><title>Natural history of allergic sensitization in infants with early-onset atopic dermatitis: results from ORCA Study</title><title>Pediatric allergy and immunology</title><addtitle>Pediatr Allergy Immunol</addtitle><description>Background Early‐onset atopic dermatitis (AD) is a particular phenotype that may convey a risk of developing multiple sensitizations to allergens but little is known about the pathway of sensitization. The aims of this study were to describe the natural history of sensitization to allergens for this phenotype and to identify the most predictive marker associated with the risk of developing sensitization to inhaled allergens in a well‐selected cohort of infants with AD. Methods Infants with active AD were enrolled and prospectively explored for biological markers of atopy every year until the age of 6 yr. Allergic sensitization was defined as the presence of positive specific IgEs to allergens and multiple sensitizations as being sensitized to ≥2 allergens. Elevated blood eosinophilia was defined as an eosinophil blood count ≥470 eosinophils/mm3 and elevated total IgE as a serum IgE level ≥45 kU/l. Results Two hundred and twenty‐nine infants were included. Elevated blood eosinophilia was observed at baseline in 60 children (26.2%) and elevated total IgE in 85 (37.1%). When elevated at baseline, eosinophilia and IgE levels remained significantly higher during the follow‐up period. Sensitization to food allergens decreased from 58% to 34%, whereas sensitization to inhaled allergens increased over time from 17% to 67%. Initial multiple sensitizations to food allergens were the most predictive factor for the risk of developing sensitization to inhaled allergens at 6 yr (OR 3.72 [1.68–8.30] p &lt; 0.001). Conclusions In the early‐onset AD phenotype, multiple sensitization to food allergens conveys a higher risk of sensitization to inhaled allergens than single sensitization.</description><subject>Age of Onset</subject><subject>Allergens - adverse effects</subject><subject>Allergens - immunology</subject><subject>Allergies</subject><subject>atopic dermatitis</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>cohort</subject><subject>Cohort Studies</subject><subject>Dermatitis</subject><subject>Dermatitis, Atopic - epidemiology</subject><subject>Dermatitis, Atopic - immunology</subject><subject>Eosinophilia - epidemiology</subject><subject>Eosinophilia - immunology</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Food - adverse effects</subject><subject>food allergens</subject><subject>Food Hypersensitivity - epidemiology</subject><subject>Food Hypersensitivity - immunology</subject><subject>Genotype &amp; phenotype</subject><subject>Humans</subject><subject>Immunization</subject><subject>Immunoglobulin E - blood</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>inhaled allergens</subject><subject>Male</subject><subject>Medical History Taking</subject><subject>Medical treatment</subject><subject>phenotypes</subject><subject>Prospective Studies</subject><subject>sensitization</subject><issn>0905-6157</issn><issn>1399-3038</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp10U1rFDEYB_Agil2rB7-ABLzoYdq8J-NtWbQtLNviCx5Dmkls6sxkmmSo46c3ddseBEMgl9_zJzx_AF5jdITrOZ5MOMKEKPkErDBt24Yiqp6CFWoRbwTm8gC8yPkaISypwM_BAeFEUYrYCkw7U-ZkengVcolpgdFD0_cu_QgWZjfmUMJvU0IcYbi73owlw9tQrqAzqV-aOGZXoClxqgOdS0PFJeQPMLk899X6FAd4_nmzhl_K3C0vwTNv-uxe3b-H4Nunj183p832_ORss942lhEhG9syaQS1xlOBuO8IEcwq2fLOey-QY145yy5tR6RhXLZYUY4tlZQIIRWx9BC82-dOKd7MLhc9hGxd35vRxTlrLDhhqFpa6dt_6HWc01h_VxUTTEmiRFXv98qmmHNyXk8pDCYtGiN9V4OuNei_NVT75j5xvhxc9ygf9l7B8R7cht4t_0_SF-uzh8hmP1F7cr8eJ0z6qYWkkuvvuxPdnmJ0sd0RzekffvmgfA</recordid><startdate>201411</startdate><enddate>201411</enddate><creator>Just, Jocelyne</creator><creator>Deslandes-Boutmy, Emmanuelle</creator><creator>Amat, Flore</creator><creator>Desseaux, Kristell</creator><creator>Nemni, Ariane</creator><creator>Bourrat, Emmanuelle</creator><creator>Sahraoui, Fatia</creator><creator>Pansé, Isabelle</creator><creator>Bagot, Martine</creator><creator>Fouéré, Sébastien</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</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></search><sort><creationdate>201411</creationdate><title>Natural history of allergic sensitization in infants with early-onset atopic dermatitis: results from ORCA Study</title><author>Just, Jocelyne ; Deslandes-Boutmy, Emmanuelle ; Amat, Flore ; Desseaux, Kristell ; Nemni, Ariane ; Bourrat, Emmanuelle ; Sahraoui, Fatia ; Pansé, Isabelle ; Bagot, Martine ; Fouéré, Sébastien</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4267-c947a63caf3605fd2264c8795dfff60e4f8ec4bcd27a457918351c373266782c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Age of Onset</topic><topic>Allergens - adverse effects</topic><topic>Allergens - immunology</topic><topic>Allergies</topic><topic>atopic dermatitis</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>cohort</topic><topic>Cohort Studies</topic><topic>Dermatitis</topic><topic>Dermatitis, Atopic - epidemiology</topic><topic>Dermatitis, Atopic - immunology</topic><topic>Eosinophilia - epidemiology</topic><topic>Eosinophilia - immunology</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Food - adverse effects</topic><topic>food allergens</topic><topic>Food Hypersensitivity - epidemiology</topic><topic>Food Hypersensitivity - immunology</topic><topic>Genotype &amp; phenotype</topic><topic>Humans</topic><topic>Immunization</topic><topic>Immunoglobulin E - blood</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>inhaled allergens</topic><topic>Male</topic><topic>Medical History Taking</topic><topic>Medical treatment</topic><topic>phenotypes</topic><topic>Prospective Studies</topic><topic>sensitization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Just, Jocelyne</creatorcontrib><creatorcontrib>Deslandes-Boutmy, Emmanuelle</creatorcontrib><creatorcontrib>Amat, Flore</creatorcontrib><creatorcontrib>Desseaux, Kristell</creatorcontrib><creatorcontrib>Nemni, Ariane</creatorcontrib><creatorcontrib>Bourrat, Emmanuelle</creatorcontrib><creatorcontrib>Sahraoui, Fatia</creatorcontrib><creatorcontrib>Pansé, Isabelle</creatorcontrib><creatorcontrib>Bagot, Martine</creatorcontrib><creatorcontrib>Fouéré, Sébastien</creatorcontrib><collection>Istex</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 &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; 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>Just, Jocelyne</au><au>Deslandes-Boutmy, Emmanuelle</au><au>Amat, Flore</au><au>Desseaux, Kristell</au><au>Nemni, Ariane</au><au>Bourrat, Emmanuelle</au><au>Sahraoui, Fatia</au><au>Pansé, Isabelle</au><au>Bagot, Martine</au><au>Fouéré, Sébastien</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Natural history of allergic sensitization in infants with early-onset atopic dermatitis: results from ORCA Study</atitle><jtitle>Pediatric allergy and immunology</jtitle><addtitle>Pediatr Allergy Immunol</addtitle><date>2014-11</date><risdate>2014</risdate><volume>25</volume><issue>7</issue><spage>668</spage><epage>673</epage><pages>668-673</pages><issn>0905-6157</issn><eissn>1399-3038</eissn><abstract>Background Early‐onset atopic dermatitis (AD) is a particular phenotype that may convey a risk of developing multiple sensitizations to allergens but little is known about the pathway of sensitization. The aims of this study were to describe the natural history of sensitization to allergens for this phenotype and to identify the most predictive marker associated with the risk of developing sensitization to inhaled allergens in a well‐selected cohort of infants with AD. Methods Infants with active AD were enrolled and prospectively explored for biological markers of atopy every year until the age of 6 yr. Allergic sensitization was defined as the presence of positive specific IgEs to allergens and multiple sensitizations as being sensitized to ≥2 allergens. Elevated blood eosinophilia was defined as an eosinophil blood count ≥470 eosinophils/mm3 and elevated total IgE as a serum IgE level ≥45 kU/l. Results Two hundred and twenty‐nine infants were included. Elevated blood eosinophilia was observed at baseline in 60 children (26.2%) and elevated total IgE in 85 (37.1%). When elevated at baseline, eosinophilia and IgE levels remained significantly higher during the follow‐up period. Sensitization to food allergens decreased from 58% to 34%, whereas sensitization to inhaled allergens increased over time from 17% to 67%. Initial multiple sensitizations to food allergens were the most predictive factor for the risk of developing sensitization to inhaled allergens at 6 yr (OR 3.72 [1.68–8.30] p &lt; 0.001). Conclusions In the early‐onset AD phenotype, multiple sensitization to food allergens conveys a higher risk of sensitization to inhaled allergens than single sensitization.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>25283304</pmid><doi>10.1111/pai.12287</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source Wiley-Blackwell Read & Publish Collection
subjects Age of Onset
Allergens - adverse effects
Allergens - immunology
Allergies
atopic dermatitis
Child
Child, Preschool
cohort
Cohort Studies
Dermatitis
Dermatitis, Atopic - epidemiology
Dermatitis, Atopic - immunology
Eosinophilia - epidemiology
Eosinophilia - immunology
Female
Follow-Up Studies
Food - adverse effects
food allergens
Food Hypersensitivity - epidemiology
Food Hypersensitivity - immunology
Genotype & phenotype
Humans
Immunization
Immunoglobulin E - blood
Infant
Infant, Newborn
inhaled allergens
Male
Medical History Taking
Medical treatment
phenotypes
Prospective Studies
sensitization
title Natural history of allergic sensitization in infants with early-onset atopic dermatitis: results from ORCA Study
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