PO-0607b Metabolomic Determinants Of Necrotizing Enterocolitis In Preterm Piglets
Background and aimStudies in premature infants and animals show that carbohydrate malabsorption and gut microbiota colonisation are key elements for triggering necrotizing enterocolitis (NEC). Our aim was to determine how dietary carbohydrate composition affects the metabolomic profile and whether u...
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Veröffentlicht in: | Archives of disease in childhood 2014-10, Vol.99 (Suppl 2), p.A451-A451 |
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description | Background and aimStudies in premature infants and animals show that carbohydrate malabsorption and gut microbiota colonisation are key elements for triggering necrotizing enterocolitis (NEC). Our aim was to determine how dietary carbohydrate composition affects the metabolomic profile and whether unique metabolite signatures correlate with NEC incidence.MethodsCecal contents and plasma were collected from a group of preterm pigs at birth and from three groups fed formula containing either lactose, corn syrup solids (CSS) or a 1:1 mixture of lactose:CSS (MIX) as the sole carbohydrate. We performed metabolomic analysis by LC/GC mass spectroscopy, clinical and histological NEC scoring, and distal ileum tissue expression of inflammatory markers.ResultsBased on clinical and histological scores NEC incidence rates were 12%, 35%, and 40% in the lactose, CSS and MIX groups, respectively. Ileum inflammatory markers (IL-8, IL-6, and IL1b) were highest in CSS vs. MIX and lactose groups and also correlated with NEC. Metabolomic analysis showed that lactose vs. CSS formula increased abundance of several cecal endocannabinoids. CSS and MIX formula increased plasma histamine, cecal and plasma lactate, beta-hydroxybutyrate, and butanediol, and decreased the abundance of several primary and secondary bile acids vs. lactose fed pigs.ConclusionsWe conclude that lactose-based formula protects against inflammation and NEC and that this correlates with increased cecal levels of anti-inflammatory neurotransmitters and reduced levels of carbohydrate fermentation products and bile acids. This novel finding suggests that endocannabinoids, normally found in breast milk, may be produced endogenously and modulate inflammation in preterm neonates fed a lactose-based formula. |
doi_str_mv | 10.1136/archdischild-2014-307384.1248 |
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Our aim was to determine how dietary carbohydrate composition affects the metabolomic profile and whether unique metabolite signatures correlate with NEC incidence.MethodsCecal contents and plasma were collected from a group of preterm pigs at birth and from three groups fed formula containing either lactose, corn syrup solids (CSS) or a 1:1 mixture of lactose:CSS (MIX) as the sole carbohydrate. We performed metabolomic analysis by LC/GC mass spectroscopy, clinical and histological NEC scoring, and distal ileum tissue expression of inflammatory markers.ResultsBased on clinical and histological scores NEC incidence rates were 12%, 35%, and 40% in the lactose, CSS and MIX groups, respectively. Ileum inflammatory markers (IL-8, IL-6, and IL1b) were highest in CSS vs. MIX and lactose groups and also correlated with NEC. Metabolomic analysis showed that lactose vs. CSS formula increased abundance of several cecal endocannabinoids. CSS and MIX formula increased plasma histamine, cecal and plasma lactate, beta-hydroxybutyrate, and butanediol, and decreased the abundance of several primary and secondary bile acids vs. lactose fed pigs.ConclusionsWe conclude that lactose-based formula protects against inflammation and NEC and that this correlates with increased cecal levels of anti-inflammatory neurotransmitters and reduced levels of carbohydrate fermentation products and bile acids. This novel finding suggests that endocannabinoids, normally found in breast milk, may be produced endogenously and modulate inflammation in preterm neonates fed a lactose-based formula.</description><identifier>ISSN: 0003-9888</identifier><identifier>EISSN: 1468-2044</identifier><identifier>DOI: 10.1136/archdischild-2014-307384.1248</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><subject>Abundance ; Acids ; Bile ; Bile acids ; Breast milk ; Cannabinoids ; Carbohydrate composition ; Carbohydrates ; Cecum ; Enterocolitis ; Fermentation ; Gastrointestinal diseases ; Histamine ; Ileum ; Infants ; Inflammation ; Interleukin 1 ; Interleukin 6 ; Interleukin 8 ; Intestinal microflora ; Lactic acid ; Lactose ; Malabsorption ; Mass spectroscopy ; Metabolites ; Metabolomics ; Microbiota ; Necrosis ; Necrotizing enterocolitis ; Neonates ; Neurotransmitters ; Syrups</subject><ispartof>Archives of disease in childhood, 2014-10, Vol.99 (Suppl 2), p.A451-A451</ispartof><rights>2014 2014, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3196,27924,27925</link.rule.ids></links><search><creatorcontrib>Call, L</creatorcontrib><creatorcontrib>Stoll, B</creatorcontrib><creatorcontrib>Garcia, S</creatorcontrib><creatorcontrib>Bauchart-Thevret, C</creatorcontrib><creatorcontrib>Donnelly, J</creatorcontrib><creatorcontrib>Sheikh, F</creatorcontrib><creatorcontrib>Akinkuotu, A</creatorcontrib><creatorcontrib>Olutoye, O</creatorcontrib><creatorcontrib>Wittke, A</creatorcontrib><creatorcontrib>Burrin, D</creatorcontrib><title>PO-0607b Metabolomic Determinants Of Necrotizing Enterocolitis In Preterm Piglets</title><title>Archives of disease in childhood</title><description>Background and aimStudies in premature infants and animals show that carbohydrate malabsorption and gut microbiota colonisation are key elements for triggering necrotizing enterocolitis (NEC). Our aim was to determine how dietary carbohydrate composition affects the metabolomic profile and whether unique metabolite signatures correlate with NEC incidence.MethodsCecal contents and plasma were collected from a group of preterm pigs at birth and from three groups fed formula containing either lactose, corn syrup solids (CSS) or a 1:1 mixture of lactose:CSS (MIX) as the sole carbohydrate. We performed metabolomic analysis by LC/GC mass spectroscopy, clinical and histological NEC scoring, and distal ileum tissue expression of inflammatory markers.ResultsBased on clinical and histological scores NEC incidence rates were 12%, 35%, and 40% in the lactose, CSS and MIX groups, respectively. Ileum inflammatory markers (IL-8, IL-6, and IL1b) were highest in CSS vs. MIX and lactose groups and also correlated with NEC. Metabolomic analysis showed that lactose vs. CSS formula increased abundance of several cecal endocannabinoids. CSS and MIX formula increased plasma histamine, cecal and plasma lactate, beta-hydroxybutyrate, and butanediol, and decreased the abundance of several primary and secondary bile acids vs. lactose fed pigs.ConclusionsWe conclude that lactose-based formula protects against inflammation and NEC and that this correlates with increased cecal levels of anti-inflammatory neurotransmitters and reduced levels of carbohydrate fermentation products and bile acids. This novel finding suggests that endocannabinoids, normally found in breast milk, may be produced endogenously and modulate inflammation in preterm neonates fed a lactose-based formula.</description><subject>Abundance</subject><subject>Acids</subject><subject>Bile</subject><subject>Bile acids</subject><subject>Breast milk</subject><subject>Cannabinoids</subject><subject>Carbohydrate composition</subject><subject>Carbohydrates</subject><subject>Cecum</subject><subject>Enterocolitis</subject><subject>Fermentation</subject><subject>Gastrointestinal diseases</subject><subject>Histamine</subject><subject>Ileum</subject><subject>Infants</subject><subject>Inflammation</subject><subject>Interleukin 1</subject><subject>Interleukin 6</subject><subject>Interleukin 8</subject><subject>Intestinal microflora</subject><subject>Lactic acid</subject><subject>Lactose</subject><subject>Malabsorption</subject><subject>Mass spectroscopy</subject><subject>Metabolites</subject><subject>Metabolomics</subject><subject>Microbiota</subject><subject>Necrosis</subject><subject>Necrotizing enterocolitis</subject><subject>Neonates</subject><subject>Neurotransmitters</subject><subject>Syrups</subject><issn>0003-9888</issn><issn>1468-2044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpNkD1PwzAQhi0EEqXwHyIhxpRznDiXgQGVApWAVgJmy_FH6ypNiu0OMLHwR_klpJSB6aS7R_fqfQi5oDCilPFL6dVSu6CWrtFpBjRPGZQM8xHNcjwgA5pz7Pd5fkgGAMDSChGPyUkIKwCaIbIBeZ7PUuBQ1t-fX48myrprurVTyY2Jxq9dK9sYkplNnozyXXQfrl0kk7a_daprXHQhmbbJ3P_SydwtGhPDKTmysgnm7G8Oyevt5GV8nz7M7qbj64dUUVZiymsmc42gpWYV4xaxsEVhqwK1sRSpVpYh6kxBWVayMKXimme81nXFLK-RDcn5_u_Gd29bE6JYdVvf9pEiowyhBApZT13tqb5ACN5YsfFuLf27oCB2HsV_j2LnUew9ip1H9gMRqGt_</recordid><startdate>201410</startdate><enddate>201410</enddate><creator>Call, L</creator><creator>Stoll, B</creator><creator>Garcia, 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Enterocolitis In Preterm Piglets</title><author>Call, L ; Stoll, B ; Garcia, S ; Bauchart-Thevret, C ; Donnelly, J ; Sheikh, F ; Akinkuotu, A ; Olutoye, O ; Wittke, A ; Burrin, D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1378-6b3a4d80dad3936f885f55f958def181dcf388d2c0779a5e7c6d626bdb93f6b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Abundance</topic><topic>Acids</topic><topic>Bile</topic><topic>Bile acids</topic><topic>Breast milk</topic><topic>Cannabinoids</topic><topic>Carbohydrate composition</topic><topic>Carbohydrates</topic><topic>Cecum</topic><topic>Enterocolitis</topic><topic>Fermentation</topic><topic>Gastrointestinal diseases</topic><topic>Histamine</topic><topic>Ileum</topic><topic>Infants</topic><topic>Inflammation</topic><topic>Interleukin 1</topic><topic>Interleukin 6</topic><topic>Interleukin 8</topic><topic>Intestinal microflora</topic><topic>Lactic acid</topic><topic>Lactose</topic><topic>Malabsorption</topic><topic>Mass spectroscopy</topic><topic>Metabolites</topic><topic>Metabolomics</topic><topic>Microbiota</topic><topic>Necrosis</topic><topic>Necrotizing enterocolitis</topic><topic>Neonates</topic><topic>Neurotransmitters</topic><topic>Syrups</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Call, L</creatorcontrib><creatorcontrib>Stoll, B</creatorcontrib><creatorcontrib>Garcia, S</creatorcontrib><creatorcontrib>Bauchart-Thevret, C</creatorcontrib><creatorcontrib>Donnelly, J</creatorcontrib><creatorcontrib>Sheikh, F</creatorcontrib><creatorcontrib>Akinkuotu, A</creatorcontrib><creatorcontrib>Olutoye, O</creatorcontrib><creatorcontrib>Wittke, A</creatorcontrib><creatorcontrib>Burrin, D</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Social Sciences Premium Collection【Remote access available】</collection><collection>ProQuest 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childhood</jtitle><date>2014-10</date><risdate>2014</risdate><volume>99</volume><issue>Suppl 2</issue><spage>A451</spage><epage>A451</epage><pages>A451-A451</pages><issn>0003-9888</issn><eissn>1468-2044</eissn><abstract>Background and aimStudies in premature infants and animals show that carbohydrate malabsorption and gut microbiota colonisation are key elements for triggering necrotizing enterocolitis (NEC). Our aim was to determine how dietary carbohydrate composition affects the metabolomic profile and whether unique metabolite signatures correlate with NEC incidence.MethodsCecal contents and plasma were collected from a group of preterm pigs at birth and from three groups fed formula containing either lactose, corn syrup solids (CSS) or a 1:1 mixture of lactose:CSS (MIX) as the sole carbohydrate. We performed metabolomic analysis by LC/GC mass spectroscopy, clinical and histological NEC scoring, and distal ileum tissue expression of inflammatory markers.ResultsBased on clinical and histological scores NEC incidence rates were 12%, 35%, and 40% in the lactose, CSS and MIX groups, respectively. Ileum inflammatory markers (IL-8, IL-6, and IL1b) were highest in CSS vs. MIX and lactose groups and also correlated with NEC. Metabolomic analysis showed that lactose vs. CSS formula increased abundance of several cecal endocannabinoids. CSS and MIX formula increased plasma histamine, cecal and plasma lactate, beta-hydroxybutyrate, and butanediol, and decreased the abundance of several primary and secondary bile acids vs. lactose fed pigs.ConclusionsWe conclude that lactose-based formula protects against inflammation and NEC and that this correlates with increased cecal levels of anti-inflammatory neurotransmitters and reduced levels of carbohydrate fermentation products and bile acids. This novel finding suggests that endocannabinoids, normally found in breast milk, may be produced endogenously and modulate inflammation in preterm neonates fed a lactose-based formula.</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/archdischild-2014-307384.1248</doi><oa>free_for_read</oa></addata></record> |
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subjects | Abundance Acids Bile Bile acids Breast milk Cannabinoids Carbohydrate composition Carbohydrates Cecum Enterocolitis Fermentation Gastrointestinal diseases Histamine Ileum Infants Inflammation Interleukin 1 Interleukin 6 Interleukin 8 Intestinal microflora Lactic acid Lactose Malabsorption Mass spectroscopy Metabolites Metabolomics Microbiota Necrosis Necrotizing enterocolitis Neonates Neurotransmitters Syrups |
title | PO-0607b Metabolomic Determinants Of Necrotizing Enterocolitis In Preterm Piglets |
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