Using Eosinophil Biomarkers From Rectal Epithelial Samples to Diagnose Food Protein-induced Proctocolitis: A Pilot Study
OBJECTIVES:The gold standard diagnostic procedure for food protein-induced proctocolitis (FPIP) requires flexible sigmoidoscopy (FS). To date there is no validated, noninvasive test to confirm FPIP diagnosis. Eosinophil-derived neurotoxin (EDN), a product of eosinophil (EOS) degranulation, has been...
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Veröffentlicht in: | Journal of pediatric gastroenterology and nutrition 2020-10, Vol.71 (4), p.e109-e112 |
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creator | de Boer, Justin Deb, Chirajyoti Bornstein, Jeffrey Horvath, Karoly Mehta, Devendra Smadi, Yamen |
description | OBJECTIVES:The gold standard diagnostic procedure for food protein-induced proctocolitis (FPIP) requires flexible sigmoidoscopy (FS). To date there is no validated, noninvasive test to confirm FPIP diagnosis. Eosinophil-derived neurotoxin (EDN), a product of eosinophil (EOS) degranulation, has been shown to correlate with eosinophil infiltration in other tissues. Our objective was to compare EDN concentrations in rectal epithelial samples from infants with FPIP with those from a control population.
METHODS:Children who underwent routine FS at Arnold Palmer Hospital for Children were enrolled in an IRB-approved, prospective, open-label pilot study between July 2017 and May 2019. We obtained rectal epithelial samples viarectal swab, cytology brushing through FS, and rectal biopsy through FS. We then measured EDN levels in the samples and compared levels found in infants with FPIP against levels found in the control group. FPIP was defined as more than 60 EOS per 10 high-power fields (HPF) in rectal epithelial tissue obtained via rectosigmoid biopsy.
RESULTS:Twenty-four patients were enrolled. The control group (n = 13) included patients with normal histopathology (84% boys, mean age 19 months, SD 6 months) and the FPIP group (n = 11) included patients with FPIP confirmed via biopsy (45% boys, mean age 6.9 months, SD 9 months). EDN concentration was significantly higher in the FPIP group than in the control group, for 2 sampling methodsrectal biopsy (183.6 ± 114.6 vs 76.6 ± 71.0 μg/mL; P = 0.010) and rectal swab (66.2 ± 64.8 vs 20.4 ± 22.2 μg/mL; P = 0.025).
CONCLUSIONS:EDN concentrations measured from rectal swab and rectal biopsy samples is elevated and may be a useful tool to screen for FPIP in children. |
doi_str_mv | 10.1097/MPG.0000000000002812 |
format | Article |
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METHODS:Children who underwent routine FS at Arnold Palmer Hospital for Children were enrolled in an IRB-approved, prospective, open-label pilot study between July 2017 and May 2019. We obtained rectal epithelial samples viarectal swab, cytology brushing through FS, and rectal biopsy through FS. We then measured EDN levels in the samples and compared levels found in infants with FPIP against levels found in the control group. FPIP was defined as more than 60 EOS per 10 high-power fields (HPF) in rectal epithelial tissue obtained via rectosigmoid biopsy.
RESULTS:Twenty-four patients were enrolled. The control group (n = 13) included patients with normal histopathology (84% boys, mean age 19 months, SD 6 months) and the FPIP group (n = 11) included patients with FPIP confirmed via biopsy (45% boys, mean age 6.9 months, SD 9 months). EDN concentration was significantly higher in the FPIP group than in the control group, for 2 sampling methodsrectal biopsy (183.6 ± 114.6 vs 76.6 ± 71.0 μg/mL; P = 0.010) and rectal swab (66.2 ± 64.8 vs 20.4 ± 22.2 μg/mL; P = 0.025).
CONCLUSIONS:EDN concentrations measured from rectal swab and rectal biopsy samples is elevated and may be a useful tool to screen for FPIP in children.</description><identifier>ISSN: 0277-2116</identifier><identifier>EISSN: 1536-4801</identifier><identifier>DOI: 10.1097/MPG.0000000000002812</identifier><identifier>PMID: 32960539</identifier><language>eng</language><publisher>United States: Lippincott Williams & Wilkins</publisher><subject>Biomarkers ; Child ; Eosinophil-Derived Neurotoxin ; Eosinophils ; Female ; Humans ; Infant ; Male ; Pilot Projects ; Proctocolitis - diagnosis ; Prospective Studies</subject><ispartof>Journal of pediatric gastroenterology and nutrition, 2020-10, Vol.71 (4), p.e109-e112</ispartof><rights>Lippincott Williams & Wilkins</rights><rights>2020 by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3502-f793ed60389ec879859cd80d084f121969f5da493223153df9a92907ca040df03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32960539$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Boer, Justin</creatorcontrib><creatorcontrib>Deb, Chirajyoti</creatorcontrib><creatorcontrib>Bornstein, Jeffrey</creatorcontrib><creatorcontrib>Horvath, Karoly</creatorcontrib><creatorcontrib>Mehta, Devendra</creatorcontrib><creatorcontrib>Smadi, Yamen</creatorcontrib><title>Using Eosinophil Biomarkers From Rectal Epithelial Samples to Diagnose Food Protein-induced Proctocolitis: A Pilot Study</title><title>Journal of pediatric gastroenterology and nutrition</title><addtitle>J Pediatr Gastroenterol Nutr</addtitle><description>OBJECTIVES:The gold standard diagnostic procedure for food protein-induced proctocolitis (FPIP) requires flexible sigmoidoscopy (FS). To date there is no validated, noninvasive test to confirm FPIP diagnosis. Eosinophil-derived neurotoxin (EDN), a product of eosinophil (EOS) degranulation, has been shown to correlate with eosinophil infiltration in other tissues. Our objective was to compare EDN concentrations in rectal epithelial samples from infants with FPIP with those from a control population.
METHODS:Children who underwent routine FS at Arnold Palmer Hospital for Children were enrolled in an IRB-approved, prospective, open-label pilot study between July 2017 and May 2019. We obtained rectal epithelial samples viarectal swab, cytology brushing through FS, and rectal biopsy through FS. We then measured EDN levels in the samples and compared levels found in infants with FPIP against levels found in the control group. FPIP was defined as more than 60 EOS per 10 high-power fields (HPF) in rectal epithelial tissue obtained via rectosigmoid biopsy.
RESULTS:Twenty-four patients were enrolled. The control group (n = 13) included patients with normal histopathology (84% boys, mean age 19 months, SD 6 months) and the FPIP group (n = 11) included patients with FPIP confirmed via biopsy (45% boys, mean age 6.9 months, SD 9 months). EDN concentration was significantly higher in the FPIP group than in the control group, for 2 sampling methodsrectal biopsy (183.6 ± 114.6 vs 76.6 ± 71.0 μg/mL; P = 0.010) and rectal swab (66.2 ± 64.8 vs 20.4 ± 22.2 μg/mL; P = 0.025).
CONCLUSIONS:EDN concentrations measured from rectal swab and rectal biopsy samples is elevated and may be a useful tool to screen for FPIP in children.</description><subject>Biomarkers</subject><subject>Child</subject><subject>Eosinophil-Derived Neurotoxin</subject><subject>Eosinophils</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Male</subject><subject>Pilot Projects</subject><subject>Proctocolitis - diagnosis</subject><subject>Prospective Studies</subject><issn>0277-2116</issn><issn>1536-4801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkNtKAzEQhoMoth7eQCQvsDpJ9hTvam1VUCwerpeYZN3YtFk2WdS3N7Uq4oUODDMD___DfAgdEDgiwIvj69n5EfwoWhK6gYYkY3mSlkA20RBoUSSUkHyAdrx_jqIizWAbDRjlOWSMD9HrgzfLJzxxcbi2MRafGrcQ3Vx3Hk87t8C3WgZh8aQ1odHWxPVOLFqrPQ4OnxnxtHRe46lzCs86F7RZJmapeqk_bhmcdNYE40_wCM-MdQHfhV697aGtWliv9z_nLnqYTu7HF8nVzfnleHSVSJYBTeqCM61yYCXXsix4mXGpSlBQpjWhhOe8zpRIOaOUxddVzQWnHAopIAVVA9tF6TpXds77TtdV25n44FtFoFqBrCLI6jfIaDtc29r-caHVt-mLXBSUa8GLsyHCmtv-RXdVo4UNzX_Z6R_WlSwjRZ5QoEBWVxKbpOwdieyPMg</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>de Boer, Justin</creator><creator>Deb, Chirajyoti</creator><creator>Bornstein, Jeffrey</creator><creator>Horvath, Karoly</creator><creator>Mehta, Devendra</creator><creator>Smadi, Yamen</creator><general>Lippincott Williams & Wilkins</general><general>by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology</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></search><sort><creationdate>20201001</creationdate><title>Using Eosinophil Biomarkers From Rectal Epithelial Samples to Diagnose Food Protein-induced Proctocolitis: A Pilot Study</title><author>de Boer, Justin ; Deb, Chirajyoti ; Bornstein, Jeffrey ; Horvath, Karoly ; Mehta, Devendra ; Smadi, Yamen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3502-f793ed60389ec879859cd80d084f121969f5da493223153df9a92907ca040df03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Biomarkers</topic><topic>Child</topic><topic>Eosinophil-Derived Neurotoxin</topic><topic>Eosinophils</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Male</topic><topic>Pilot Projects</topic><topic>Proctocolitis - diagnosis</topic><topic>Prospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Boer, Justin</creatorcontrib><creatorcontrib>Deb, Chirajyoti</creatorcontrib><creatorcontrib>Bornstein, Jeffrey</creatorcontrib><creatorcontrib>Horvath, Karoly</creatorcontrib><creatorcontrib>Mehta, Devendra</creatorcontrib><creatorcontrib>Smadi, Yamen</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Boer, Justin</au><au>Deb, Chirajyoti</au><au>Bornstein, Jeffrey</au><au>Horvath, Karoly</au><au>Mehta, Devendra</au><au>Smadi, Yamen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Using Eosinophil Biomarkers From Rectal Epithelial Samples to Diagnose Food Protein-induced Proctocolitis: A Pilot Study</atitle><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle><addtitle>J Pediatr Gastroenterol Nutr</addtitle><date>2020-10-01</date><risdate>2020</risdate><volume>71</volume><issue>4</issue><spage>e109</spage><epage>e112</epage><pages>e109-e112</pages><issn>0277-2116</issn><eissn>1536-4801</eissn><abstract>OBJECTIVES:The gold standard diagnostic procedure for food protein-induced proctocolitis (FPIP) requires flexible sigmoidoscopy (FS). To date there is no validated, noninvasive test to confirm FPIP diagnosis. Eosinophil-derived neurotoxin (EDN), a product of eosinophil (EOS) degranulation, has been shown to correlate with eosinophil infiltration in other tissues. Our objective was to compare EDN concentrations in rectal epithelial samples from infants with FPIP with those from a control population.
METHODS:Children who underwent routine FS at Arnold Palmer Hospital for Children were enrolled in an IRB-approved, prospective, open-label pilot study between July 2017 and May 2019. We obtained rectal epithelial samples viarectal swab, cytology brushing through FS, and rectal biopsy through FS. We then measured EDN levels in the samples and compared levels found in infants with FPIP against levels found in the control group. FPIP was defined as more than 60 EOS per 10 high-power fields (HPF) in rectal epithelial tissue obtained via rectosigmoid biopsy.
RESULTS:Twenty-four patients were enrolled. The control group (n = 13) included patients with normal histopathology (84% boys, mean age 19 months, SD 6 months) and the FPIP group (n = 11) included patients with FPIP confirmed via biopsy (45% boys, mean age 6.9 months, SD 9 months). EDN concentration was significantly higher in the FPIP group than in the control group, for 2 sampling methodsrectal biopsy (183.6 ± 114.6 vs 76.6 ± 71.0 μg/mL; P = 0.010) and rectal swab (66.2 ± 64.8 vs 20.4 ± 22.2 μg/mL; P = 0.025).
CONCLUSIONS:EDN concentrations measured from rectal swab and rectal biopsy samples is elevated and may be a useful tool to screen for FPIP in children.</abstract><cop>United States</cop><pub>Lippincott Williams & Wilkins</pub><pmid>32960539</pmid><doi>10.1097/MPG.0000000000002812</doi></addata></record> |
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subjects | Biomarkers Child Eosinophil-Derived Neurotoxin Eosinophils Female Humans Infant Male Pilot Projects Proctocolitis - diagnosis Prospective Studies |
title | Using Eosinophil Biomarkers From Rectal Epithelial Samples to Diagnose Food Protein-induced Proctocolitis: A Pilot Study |
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