Factors that predict the clinical reactivity and tolerance in children with cow's milk allergy
Abstract Background Specific IgE (sIgE) may be used for the diagnosis of cow's milk allergy (CMA) and as a guide to perform food challenge tests in patients with CMA. The effect of genetic variants on the prognosis of food allergy is largely unknown. Objective To examine the performance of sIgE...
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creator | Yavuz, S. Tolga, MD Buyuktiryaki, Betul, MD Sahiner, Umit M., MD Birben, Esra, PhD Tuncer, Ayfer, MD Yakarisik, Selin, MD Karabulut, Erdem, PhD Kalayci, Omer, MD Sackesen, Cansin, MD |
description | Abstract Background Specific IgE (sIgE) may be used for the diagnosis of cow's milk allergy (CMA) and as a guide to perform food challenge tests in patients with CMA. The effect of genetic variants on the prognosis of food allergy is largely unknown. Objective To examine the performance of sIgE analysis and the utility of the genetic variants of CD14, STAT6, IL13, IL10, SPINK5 , and TSLP in predicting the clinical course in children with CMA. Methods Serum sIgE levels of 94 children who underwent open food challenges and 54 children with anaphylaxis due to cow's milk (CM) were retrospectively analyzed between January 2002 and May 2009. The genetic polymorphisms were determined in 72 children. Results A total of 148 children were followed up for a median of 3.5 years, and 42 of the 94 challenge results were positive. The probability curves with 95% decision points were 2.8 kU/L for younger than 1 year, 11.1 for younger than 2 years, 11.7 for younger than 4 years, and 13.7 for younger than 6 years. Sixty-six children outgrew CMA during follow-up. Children with initial an CM sIgE level less than 6 kU/L outgrew CMA earlier than children with an initial CM sIgE level of 6 kU/L or higher ( P < .001). The age of tolerance development for CM was significantly higher in children with the GG genotype at rs324015 of the STAT6 gene compared with those with the AA+AG genotype (2 years [range, 1.5-3.9 years] vs 1.2 years [range, 1.0-2.2 years]) ( P = .02). Conclusion The decision points of sIgE obtained in different age groups may help to determine the likelihood of clinical reactivity more precisely. The results suggest that sIgE levels and STAT6 gene variants may be important determinants to predict longer persistence of CMA. |
doi_str_mv | 10.1016/j.anai.2013.01.018 |
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Tolga, MD ; Buyuktiryaki, Betul, MD ; Sahiner, Umit M., MD ; Birben, Esra, PhD ; Tuncer, Ayfer, MD ; Yakarisik, Selin, MD ; Karabulut, Erdem, PhD ; Kalayci, Omer, MD ; Sackesen, Cansin, MD</creator><creatorcontrib>Yavuz, S. Tolga, MD ; Buyuktiryaki, Betul, MD ; Sahiner, Umit M., MD ; Birben, Esra, PhD ; Tuncer, Ayfer, MD ; Yakarisik, Selin, MD ; Karabulut, Erdem, PhD ; Kalayci, Omer, MD ; Sackesen, Cansin, MD</creatorcontrib><description>Abstract Background Specific IgE (sIgE) may be used for the diagnosis of cow's milk allergy (CMA) and as a guide to perform food challenge tests in patients with CMA. The effect of genetic variants on the prognosis of food allergy is largely unknown. Objective To examine the performance of sIgE analysis and the utility of the genetic variants of CD14, STAT6, IL13, IL10, SPINK5 , and TSLP in predicting the clinical course in children with CMA. Methods Serum sIgE levels of 94 children who underwent open food challenges and 54 children with anaphylaxis due to cow's milk (CM) were retrospectively analyzed between January 2002 and May 2009. The genetic polymorphisms were determined in 72 children. Results A total of 148 children were followed up for a median of 3.5 years, and 42 of the 94 challenge results were positive. The probability curves with 95% decision points were 2.8 kU/L for younger than 1 year, 11.1 for younger than 2 years, 11.7 for younger than 4 years, and 13.7 for younger than 6 years. Sixty-six children outgrew CMA during follow-up. Children with initial an CM sIgE level less than 6 kU/L outgrew CMA earlier than children with an initial CM sIgE level of 6 kU/L or higher ( P < .001). The age of tolerance development for CM was significantly higher in children with the GG genotype at rs324015 of the STAT6 gene compared with those with the AA+AG genotype (2 years [range, 1.5-3.9 years] vs 1.2 years [range, 1.0-2.2 years]) ( P = .02). Conclusion The decision points of sIgE obtained in different age groups may help to determine the likelihood of clinical reactivity more precisely. The results suggest that sIgE levels and STAT6 gene variants may be important determinants to predict longer persistence of CMA.</description><identifier>ISSN: 1081-1206</identifier><identifier>EISSN: 1534-4436</identifier><identifier>DOI: 10.1016/j.anai.2013.01.018</identifier><identifier>PMID: 23535094</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Allergy and Immunology ; Anaphylaxis - diagnosis ; Anaphylaxis - genetics ; Anaphylaxis - immunology ; Animals ; Cattle ; Child ; Child, Preschool ; Female ; Food Hypersensitivity - diagnosis ; Food Hypersensitivity - genetics ; Food Hypersensitivity - immunology ; Food Hypersensitivity - physiopathology ; Humans ; Immune Tolerance - genetics ; Immunoglobulin E - blood ; Infant ; Male ; Milk - adverse effects ; Milk - immunology ; Milk Hypersensitivity - diagnosis ; Milk Hypersensitivity - genetics ; Milk Hypersensitivity - immunology ; Polymorphism, Genetic ; Predictive Value of Tests ; Prognosis ; Risk Factors ; STAT6 Transcription Factor - genetics ; STAT6 Transcription Factor - metabolism</subject><ispartof>Annals of allergy, asthma, & immunology, 2013-04, Vol.110 (4), p.284-289</ispartof><rights>American College of Allergy, Asthma & Immunology</rights><rights>2013 American College of Allergy, Asthma & Immunology</rights><rights>Copyright © 2013 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-1992d903f6fd871649c49d1566875ad90e207b0c737e22c22c45953041892f5b3</citedby><cites>FETCH-LOGICAL-c411t-1992d903f6fd871649c49d1566875ad90e207b0c737e22c22c45953041892f5b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1081120613000513$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23535094$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yavuz, S. Tolga, MD</creatorcontrib><creatorcontrib>Buyuktiryaki, Betul, MD</creatorcontrib><creatorcontrib>Sahiner, Umit M., MD</creatorcontrib><creatorcontrib>Birben, Esra, PhD</creatorcontrib><creatorcontrib>Tuncer, Ayfer, MD</creatorcontrib><creatorcontrib>Yakarisik, Selin, MD</creatorcontrib><creatorcontrib>Karabulut, Erdem, PhD</creatorcontrib><creatorcontrib>Kalayci, Omer, MD</creatorcontrib><creatorcontrib>Sackesen, Cansin, MD</creatorcontrib><title>Factors that predict the clinical reactivity and tolerance in children with cow's milk allergy</title><title>Annals of allergy, asthma, & immunology</title><addtitle>Ann Allergy Asthma Immunol</addtitle><description>Abstract Background Specific IgE (sIgE) may be used for the diagnosis of cow's milk allergy (CMA) and as a guide to perform food challenge tests in patients with CMA. The effect of genetic variants on the prognosis of food allergy is largely unknown. Objective To examine the performance of sIgE analysis and the utility of the genetic variants of CD14, STAT6, IL13, IL10, SPINK5 , and TSLP in predicting the clinical course in children with CMA. Methods Serum sIgE levels of 94 children who underwent open food challenges and 54 children with anaphylaxis due to cow's milk (CM) were retrospectively analyzed between January 2002 and May 2009. The genetic polymorphisms were determined in 72 children. Results A total of 148 children were followed up for a median of 3.5 years, and 42 of the 94 challenge results were positive. The probability curves with 95% decision points were 2.8 kU/L for younger than 1 year, 11.1 for younger than 2 years, 11.7 for younger than 4 years, and 13.7 for younger than 6 years. Sixty-six children outgrew CMA during follow-up. Children with initial an CM sIgE level less than 6 kU/L outgrew CMA earlier than children with an initial CM sIgE level of 6 kU/L or higher ( P < .001). The age of tolerance development for CM was significantly higher in children with the GG genotype at rs324015 of the STAT6 gene compared with those with the AA+AG genotype (2 years [range, 1.5-3.9 years] vs 1.2 years [range, 1.0-2.2 years]) ( P = .02). Conclusion The decision points of sIgE obtained in different age groups may help to determine the likelihood of clinical reactivity more precisely. The results suggest that sIgE levels and STAT6 gene variants may be important determinants to predict longer persistence of CMA.</description><subject>Allergy and Immunology</subject><subject>Anaphylaxis - diagnosis</subject><subject>Anaphylaxis - genetics</subject><subject>Anaphylaxis - immunology</subject><subject>Animals</subject><subject>Cattle</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Female</subject><subject>Food Hypersensitivity - diagnosis</subject><subject>Food Hypersensitivity - genetics</subject><subject>Food Hypersensitivity - immunology</subject><subject>Food Hypersensitivity - physiopathology</subject><subject>Humans</subject><subject>Immune Tolerance - genetics</subject><subject>Immunoglobulin E - blood</subject><subject>Infant</subject><subject>Male</subject><subject>Milk - adverse effects</subject><subject>Milk - immunology</subject><subject>Milk Hypersensitivity - diagnosis</subject><subject>Milk Hypersensitivity - genetics</subject><subject>Milk Hypersensitivity - immunology</subject><subject>Polymorphism, Genetic</subject><subject>Predictive Value of Tests</subject><subject>Prognosis</subject><subject>Risk Factors</subject><subject>STAT6 Transcription Factor - genetics</subject><subject>STAT6 Transcription Factor - metabolism</subject><issn>1081-1206</issn><issn>1534-4436</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc9rFDEUx4NYbK3-Ax5KbnqZNS8_ZiZQBCmtCoUe1Kshm7xxs83ObJNsy_73zbBtDx6EB0nI533hfR4hH4AtgEH7eb2wow0LzkAsGNTqX5ETUEI2Uor2db2zHhrgrD0mb3NeM1aRVrwhx1wooZiWJ-TPlXVlSpmWlS10m9AHV-oDqYthDM5GmrAi4T6UPbWjp2WKmOzokIaRulWIPuFIH0JZUTc9fMx0E-IttbFSf_fvyNFgY8b3T-cp-X11-evie3N98-3HxdfrxkmA0oDW3GsmhnbwfQet1E5qD6pt-07Z-oOcdUvmOtEh566WVFoJJqHXfFBLcUo-HXK3abrbYS5mE7LDGO2I0y4bEBw6rXroK8oPqEtTzgkHs01hY9PeADOzV7M2s1czezUMas1NZ0_5u-UG_UvLs8gKnB8ArFPeB0wmu4DVkg8JXTF-Cv_P__JP-7P-W9xjXk-7NFZ_Bkzmhpmf82bnxYKoS1UgxCMBPZy1</recordid><startdate>20130401</startdate><enddate>20130401</enddate><creator>Yavuz, S. Tolga, MD</creator><creator>Buyuktiryaki, Betul, MD</creator><creator>Sahiner, Umit M., MD</creator><creator>Birben, Esra, PhD</creator><creator>Tuncer, Ayfer, MD</creator><creator>Yakarisik, Selin, MD</creator><creator>Karabulut, Erdem, PhD</creator><creator>Kalayci, Omer, MD</creator><creator>Sackesen, Cansin, MD</creator><general>Elsevier Inc</general><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>20130401</creationdate><title>Factors that predict the clinical reactivity and tolerance in children with cow's milk allergy</title><author>Yavuz, S. Tolga, MD ; Buyuktiryaki, Betul, MD ; Sahiner, Umit M., MD ; Birben, Esra, PhD ; Tuncer, Ayfer, MD ; Yakarisik, Selin, MD ; Karabulut, Erdem, PhD ; Kalayci, Omer, MD ; Sackesen, Cansin, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-1992d903f6fd871649c49d1566875ad90e207b0c737e22c22c45953041892f5b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Allergy and Immunology</topic><topic>Anaphylaxis - diagnosis</topic><topic>Anaphylaxis - genetics</topic><topic>Anaphylaxis - immunology</topic><topic>Animals</topic><topic>Cattle</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Female</topic><topic>Food Hypersensitivity - diagnosis</topic><topic>Food Hypersensitivity - genetics</topic><topic>Food Hypersensitivity - immunology</topic><topic>Food Hypersensitivity - physiopathology</topic><topic>Humans</topic><topic>Immune Tolerance - genetics</topic><topic>Immunoglobulin E - blood</topic><topic>Infant</topic><topic>Male</topic><topic>Milk - adverse effects</topic><topic>Milk - immunology</topic><topic>Milk Hypersensitivity - diagnosis</topic><topic>Milk Hypersensitivity - genetics</topic><topic>Milk Hypersensitivity - immunology</topic><topic>Polymorphism, Genetic</topic><topic>Predictive Value of Tests</topic><topic>Prognosis</topic><topic>Risk Factors</topic><topic>STAT6 Transcription Factor - genetics</topic><topic>STAT6 Transcription Factor - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yavuz, S. Tolga, MD</creatorcontrib><creatorcontrib>Buyuktiryaki, Betul, MD</creatorcontrib><creatorcontrib>Sahiner, Umit M., MD</creatorcontrib><creatorcontrib>Birben, Esra, PhD</creatorcontrib><creatorcontrib>Tuncer, Ayfer, MD</creatorcontrib><creatorcontrib>Yakarisik, Selin, MD</creatorcontrib><creatorcontrib>Karabulut, Erdem, PhD</creatorcontrib><creatorcontrib>Kalayci, Omer, MD</creatorcontrib><creatorcontrib>Sackesen, Cansin, MD</creatorcontrib><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>Annals of allergy, asthma, & immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yavuz, S. Tolga, MD</au><au>Buyuktiryaki, Betul, MD</au><au>Sahiner, Umit M., MD</au><au>Birben, Esra, PhD</au><au>Tuncer, Ayfer, MD</au><au>Yakarisik, Selin, MD</au><au>Karabulut, Erdem, PhD</au><au>Kalayci, Omer, MD</au><au>Sackesen, Cansin, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Factors that predict the clinical reactivity and tolerance in children with cow's milk allergy</atitle><jtitle>Annals of allergy, asthma, & immunology</jtitle><addtitle>Ann Allergy Asthma Immunol</addtitle><date>2013-04-01</date><risdate>2013</risdate><volume>110</volume><issue>4</issue><spage>284</spage><epage>289</epage><pages>284-289</pages><issn>1081-1206</issn><eissn>1534-4436</eissn><abstract>Abstract Background Specific IgE (sIgE) may be used for the diagnosis of cow's milk allergy (CMA) and as a guide to perform food challenge tests in patients with CMA. The effect of genetic variants on the prognosis of food allergy is largely unknown. Objective To examine the performance of sIgE analysis and the utility of the genetic variants of CD14, STAT6, IL13, IL10, SPINK5 , and TSLP in predicting the clinical course in children with CMA. Methods Serum sIgE levels of 94 children who underwent open food challenges and 54 children with anaphylaxis due to cow's milk (CM) were retrospectively analyzed between January 2002 and May 2009. The genetic polymorphisms were determined in 72 children. Results A total of 148 children were followed up for a median of 3.5 years, and 42 of the 94 challenge results were positive. The probability curves with 95% decision points were 2.8 kU/L for younger than 1 year, 11.1 for younger than 2 years, 11.7 for younger than 4 years, and 13.7 for younger than 6 years. Sixty-six children outgrew CMA during follow-up. Children with initial an CM sIgE level less than 6 kU/L outgrew CMA earlier than children with an initial CM sIgE level of 6 kU/L or higher ( P < .001). The age of tolerance development for CM was significantly higher in children with the GG genotype at rs324015 of the STAT6 gene compared with those with the AA+AG genotype (2 years [range, 1.5-3.9 years] vs 1.2 years [range, 1.0-2.2 years]) ( P = .02). Conclusion The decision points of sIgE obtained in different age groups may help to determine the likelihood of clinical reactivity more precisely. The results suggest that sIgE levels and STAT6 gene variants may be important determinants to predict longer persistence of CMA.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23535094</pmid><doi>10.1016/j.anai.2013.01.018</doi><tpages>6</tpages></addata></record> |
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subjects | Allergy and Immunology Anaphylaxis - diagnosis Anaphylaxis - genetics Anaphylaxis - immunology Animals Cattle Child Child, Preschool Female Food Hypersensitivity - diagnosis Food Hypersensitivity - genetics Food Hypersensitivity - immunology Food Hypersensitivity - physiopathology Humans Immune Tolerance - genetics Immunoglobulin E - blood Infant Male Milk - adverse effects Milk - immunology Milk Hypersensitivity - diagnosis Milk Hypersensitivity - genetics Milk Hypersensitivity - immunology Polymorphism, Genetic Predictive Value of Tests Prognosis Risk Factors STAT6 Transcription Factor - genetics STAT6 Transcription Factor - metabolism |
title | Factors that predict the clinical reactivity and tolerance in children with cow's milk allergy |
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