Retinol concentrations after birth are inversely associated with atopic manifestations in children and young adults

Summary Background Vitamin A has anti‐inflammatory and immunomodulatory effects, and its deficiency results in impaired specific and innate immunity. Vitamin A is essential for inducing the gut‐homing specificity on T cells. Objective As an impaired gut immune response in early infancy may contribut...

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Veröffentlicht in:Clinical and experimental allergy 2007-01, Vol.37 (1), p.54-61
Hauptverfasser: Pesonen, M., Kallio, M. J. T., Siimes, M. A., Ranki, A.
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container_issue 1
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container_title Clinical and experimental allergy
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creator Pesonen, M.
Kallio, M. J. T.
Siimes, M. A.
Ranki, A.
description Summary Background Vitamin A has anti‐inflammatory and immunomodulatory effects, and its deficiency results in impaired specific and innate immunity. Vitamin A is essential for inducing the gut‐homing specificity on T cells. Objective As an impaired gut immune response in early infancy may contribute to the development of atopic sensitization, we looked for an association of plasma retinol concentrations and the subsequent development of allergic symptoms in healthy infants. Methods A cohort of 200 unselected, full‐term newborns were followed up from birth to age 20 years. The plasma retinol concentration was determined in cord blood (n=97), at ages of 2, 4 and 12 months (n=95), and at ages 5 years (n=155) and 11 years (n=151). The subjects were re‐examined at the ages of 5, 11 and 20 years with assessment of the occurrence of allergic symptoms during the preceding year, skin prick testing and measurement of serum total IgE. Results Subjects with allergic symptoms or a positive skin prick test (SPT) in childhood or adolescence had lower retinol concentrations in infancy and childhood than symptom‐free subjects. The difference was most pronounced at age 2 months. Retinol concentration at 2 months correlated inversely with positive SPT at ages of 5 and 20 years, and with allergic symptoms at age 20 years. Conclusion Retinol concentration in young infants is inversely associated with the subsequent development of allergic symptoms. We propose that an inborn regulation of retinol may play a role in atopic sensitization, possibly through regulating the intestinal T cell responses.
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J. T. ; Siimes, M. A. ; Ranki, A.</creator><creatorcontrib>Pesonen, M. ; Kallio, M. J. T. ; Siimes, M. A. ; Ranki, A.</creatorcontrib><description>Summary Background Vitamin A has anti‐inflammatory and immunomodulatory effects, and its deficiency results in impaired specific and innate immunity. Vitamin A is essential for inducing the gut‐homing specificity on T cells. Objective As an impaired gut immune response in early infancy may contribute to the development of atopic sensitization, we looked for an association of plasma retinol concentrations and the subsequent development of allergic symptoms in healthy infants. Methods A cohort of 200 unselected, full‐term newborns were followed up from birth to age 20 years. The plasma retinol concentration was determined in cord blood (n=97), at ages of 2, 4 and 12 months (n=95), and at ages 5 years (n=155) and 11 years (n=151). The subjects were re‐examined at the ages of 5, 11 and 20 years with assessment of the occurrence of allergic symptoms during the preceding year, skin prick testing and measurement of serum total IgE. Results Subjects with allergic symptoms or a positive skin prick test (SPT) in childhood or adolescence had lower retinol concentrations in infancy and childhood than symptom‐free subjects. The difference was most pronounced at age 2 months. Retinol concentration at 2 months correlated inversely with positive SPT at ages of 5 and 20 years, and with allergic symptoms at age 20 years. Conclusion Retinol concentration in young infants is inversely associated with the subsequent development of allergic symptoms. We propose that an inborn regulation of retinol may play a role in atopic sensitization, possibly through regulating the intestinal T cell responses.</description><identifier>ISSN: 0954-7894</identifier><identifier>EISSN: 1365-2222</identifier><identifier>DOI: 10.1111/j.1365-2222.2006.02630.x</identifier><identifier>PMID: 17210042</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Allergic diseases ; atopy ; Biological and medical sciences ; Case-Control Studies ; Female ; Fetal Blood - chemistry ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Humans ; Hypersensitivity - blood ; Hypersensitivity - diagnosis ; Hypersensitivity - immunology ; Immunoglobulin E - blood ; Immunopathology ; Infant, Newborn ; Logistic Models ; Longitudinal Studies ; Male ; Medical sciences ; retinol ; Sex Factors ; Skin Tests ; vitamin A ; Vitamin A - blood</subject><ispartof>Clinical and experimental allergy, 2007-01, Vol.37 (1), p.54-61</ispartof><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4350-3cedf0536d29ab25b075f4875add6e3096ab07407365a2b0c833797324da5afc3</citedby><cites>FETCH-LOGICAL-c4350-3cedf0536d29ab25b075f4875add6e3096ab07407365a2b0c833797324da5afc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2222.2006.02630.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2222.2006.02630.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,4010,27904,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=18489140$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17210042$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pesonen, M.</creatorcontrib><creatorcontrib>Kallio, M. J. T.</creatorcontrib><creatorcontrib>Siimes, M. A.</creatorcontrib><creatorcontrib>Ranki, A.</creatorcontrib><title>Retinol concentrations after birth are inversely associated with atopic manifestations in children and young adults</title><title>Clinical and experimental allergy</title><addtitle>Clin Exp Allergy</addtitle><description>Summary Background Vitamin A has anti‐inflammatory and immunomodulatory effects, and its deficiency results in impaired specific and innate immunity. Vitamin A is essential for inducing the gut‐homing specificity on T cells. Objective As an impaired gut immune response in early infancy may contribute to the development of atopic sensitization, we looked for an association of plasma retinol concentrations and the subsequent development of allergic symptoms in healthy infants. Methods A cohort of 200 unselected, full‐term newborns were followed up from birth to age 20 years. The plasma retinol concentration was determined in cord blood (n=97), at ages of 2, 4 and 12 months (n=95), and at ages 5 years (n=155) and 11 years (n=151). The subjects were re‐examined at the ages of 5, 11 and 20 years with assessment of the occurrence of allergic symptoms during the preceding year, skin prick testing and measurement of serum total IgE. Results Subjects with allergic symptoms or a positive skin prick test (SPT) in childhood or adolescence had lower retinol concentrations in infancy and childhood than symptom‐free subjects. The difference was most pronounced at age 2 months. Retinol concentration at 2 months correlated inversely with positive SPT at ages of 5 and 20 years, and with allergic symptoms at age 20 years. Conclusion Retinol concentration in young infants is inversely associated with the subsequent development of allergic symptoms. We propose that an inborn regulation of retinol may play a role in atopic sensitization, possibly through regulating the intestinal T cell responses.</description><subject>Allergic diseases</subject><subject>atopy</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>Female</subject><subject>Fetal Blood - chemistry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Humans</subject><subject>Hypersensitivity - blood</subject><subject>Hypersensitivity - diagnosis</subject><subject>Hypersensitivity - immunology</subject><subject>Immunoglobulin E - blood</subject><subject>Immunopathology</subject><subject>Infant, Newborn</subject><subject>Logistic Models</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Medical sciences</subject><subject>retinol</subject><subject>Sex Factors</subject><subject>Skin Tests</subject><subject>vitamin A</subject><subject>Vitamin A - blood</subject><issn>0954-7894</issn><issn>1365-2222</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE-P1CAYh4nRuOPqVzBc9NZK-VPag4fNZB3NbjSZaEy8kLdAXcYOHYG6M99e6jS7V98LhPf5wcuDEK5IWeV6tysrVouC5iopIXVJaM1IeXyCVg-Np2hFWsEL2bT8Ar2IcUcIYaJtnqOLStKKEE5XKG5tcn4csB69tj4FSG70EUOfbMCdC-kOQ7DY-T82RDucMMQ4agfJGnzv5m4aD07jPXjX25iWvPNY37nBBOsxeINP4-R_YjDTkOJL9KyHIdpXy3qJvn24_rr-WNx-2XxaX90WmjNBCqat6YlgtaEtdFR0RIqeN1KAMbVlpK0hH3Ei84-BdkQ3jMlWMsoNCOg1u0Rvz_cewvh7yrOpvYvaDgN4O05R1Q2vWMVoBpszqMMYY7C9OgS3h3BSFVGzcLVTs1c1e1WzcPVPuDrm6OvljanbW_MYXAxn4M0CQNQw9AG8dvGRa3jTVpxk7v2Zu3eDPf33AGp9fTXvcr44511M9viQh_BL1ZJJob5_3ij2Y7vdtPJG3bC_RcKstg</recordid><startdate>200701</startdate><enddate>200701</enddate><creator>Pesonen, M.</creator><creator>Kallio, M. J. T.</creator><creator>Siimes, M. A.</creator><creator>Ranki, A.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><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>7X8</scope></search><sort><creationdate>200701</creationdate><title>Retinol concentrations after birth are inversely associated with atopic manifestations in children and young adults</title><author>Pesonen, M. ; Kallio, M. J. T. ; Siimes, M. A. ; Ranki, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4350-3cedf0536d29ab25b075f4875add6e3096ab07407365a2b0c833797324da5afc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Allergic diseases</topic><topic>atopy</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>Female</topic><topic>Fetal Blood - chemistry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Humans</topic><topic>Hypersensitivity - blood</topic><topic>Hypersensitivity - diagnosis</topic><topic>Hypersensitivity - immunology</topic><topic>Immunoglobulin E - blood</topic><topic>Immunopathology</topic><topic>Infant, Newborn</topic><topic>Logistic Models</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Medical sciences</topic><topic>retinol</topic><topic>Sex Factors</topic><topic>Skin Tests</topic><topic>vitamin A</topic><topic>Vitamin A - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pesonen, M.</creatorcontrib><creatorcontrib>Kallio, M. J. T.</creatorcontrib><creatorcontrib>Siimes, M. A.</creatorcontrib><creatorcontrib>Ranki, A.</creatorcontrib><collection>Istex</collection><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>MEDLINE - Academic</collection><jtitle>Clinical and experimental allergy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pesonen, M.</au><au>Kallio, M. J. T.</au><au>Siimes, M. A.</au><au>Ranki, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Retinol concentrations after birth are inversely associated with atopic manifestations in children and young adults</atitle><jtitle>Clinical and experimental allergy</jtitle><addtitle>Clin Exp Allergy</addtitle><date>2007-01</date><risdate>2007</risdate><volume>37</volume><issue>1</issue><spage>54</spage><epage>61</epage><pages>54-61</pages><issn>0954-7894</issn><eissn>1365-2222</eissn><abstract>Summary Background Vitamin A has anti‐inflammatory and immunomodulatory effects, and its deficiency results in impaired specific and innate immunity. Vitamin A is essential for inducing the gut‐homing specificity on T cells. Objective As an impaired gut immune response in early infancy may contribute to the development of atopic sensitization, we looked for an association of plasma retinol concentrations and the subsequent development of allergic symptoms in healthy infants. Methods A cohort of 200 unselected, full‐term newborns were followed up from birth to age 20 years. The plasma retinol concentration was determined in cord blood (n=97), at ages of 2, 4 and 12 months (n=95), and at ages 5 years (n=155) and 11 years (n=151). The subjects were re‐examined at the ages of 5, 11 and 20 years with assessment of the occurrence of allergic symptoms during the preceding year, skin prick testing and measurement of serum total IgE. Results Subjects with allergic symptoms or a positive skin prick test (SPT) in childhood or adolescence had lower retinol concentrations in infancy and childhood than symptom‐free subjects. The difference was most pronounced at age 2 months. Retinol concentration at 2 months correlated inversely with positive SPT at ages of 5 and 20 years, and with allergic symptoms at age 20 years. Conclusion Retinol concentration in young infants is inversely associated with the subsequent development of allergic symptoms. We propose that an inborn regulation of retinol may play a role in atopic sensitization, possibly through regulating the intestinal T cell responses.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>17210042</pmid><doi>10.1111/j.1365-2222.2006.02630.x</doi><tpages>8</tpages></addata></record>
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subjects Allergic diseases
atopy
Biological and medical sciences
Case-Control Studies
Female
Fetal Blood - chemistry
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Humans
Hypersensitivity - blood
Hypersensitivity - diagnosis
Hypersensitivity - immunology
Immunoglobulin E - blood
Immunopathology
Infant, Newborn
Logistic Models
Longitudinal Studies
Male
Medical sciences
retinol
Sex Factors
Skin Tests
vitamin A
Vitamin A - blood
title Retinol concentrations after birth are inversely associated with atopic manifestations in children and young adults
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