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1000 Titel
  • Mechanisms Affecting the Gut of Preterm Infants in Enteral Feeding Trials
1000 Autor/in
  1. Embleton, Nicholas D. |
  2. Berrington, Janet E. |
  3. Dorling, Jon |
  4. Ewer, Andrew K. |
  5. Juszczak, Edmund |
  6. Kirby, John A. |
  7. Lamb, Christopher A. |
  8. Lanyon, Clare V. |
  9. McGuire, William |
  10. Probert, Christopher S. |
  11. Rushton, Stephen P. |
  12. Shirley, Mark D. |
  13. Stewart, Christopher J. |
  14. Cummings, Stephen P. |
1000 Erscheinungsjahr 2017
1000 Art der Datei
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2017-05-08
1000 Erschienen in
1000 Quellenangabe
  • 4:14
1000 Copyrightjahr
  • 2017
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.3389/fnut.2017.00014 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420562/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Large randomized controlled trials (RCTs) in preterm infants offer unique opportunities for mechanistic evaluation of the risk factors leading to serious diseases, as well as the actions of interventions designed to prevent them. Necrotizing enterocolitis (NEC) a serious inflammatory gut condition and late-onset sepsis (LOS) are common feeding and nutrition-related problems that may cause death or serious long-term morbidity and are key outcomes in two current UK National Institutes for Health Research (NIHR) trials. Speed of increasing milk feeds trial (SIFT) randomized preterm infants to different rates of increases in milk feeds with a primary outcome of survival without disability at 2 years corrected age. Enteral lactoferrin in neonates (ELFIN) randomizes infants to supplemental enteral lactoferrin or placebo with a primary outcome of LOS. This is a protocol for the mechanisms affecting the gut of preterm infants in enteral feeding trials (MAGPIE) study and is funded by the UK NIHR Efficacy and Mechanistic Evaluation programme. MAGPIE will recruit ~480 preterm infants who were enrolled in SIFT or ELFIN. Participation in MAGPIE does not change the main trial protocols and uses non-invasive sampling of stool and urine, along with any residual resected gut tissue if infants required surgery. Trial interventions may involve effects on gut microbes, metabolites (e.g., short-chain fatty acids), and aspects of host immune function. Current hypotheses suggest that NEC and/or LOS are due to a dysregulated immune system in the context of gut dysbiosis, but mechanisms have not been systematically studied within large RCTs. Microbiomic analysis will use next-generation sequencing, and metabolites will be assessed by mass spectrometry to detect volatile organic and other compounds produced by microbes or the host. We will explore differences between disease cases and controls, as well as exploring the actions of trial interventions. Impacts of this research are multiple: translation of knowledge of mechanisms promoting gut health may explain outcomes or suggest alternate strategies to improve health. Results may identify new non-invasive diagnostic or monitoring techniques, preventative or treatment strategies for NEC or LOS, or provide data useful for risk stratification in future studies. Mechanistic evaluation might be especially informative where there are not clear effects on the primary outcome (ISRCTN 12554594).
1000 Sacherschließung
lokal mechanistic evaluation
lokal necrotizing enterocolitis
lokal nutrition
lokal lactoferrin
lokal preterm infant
lokal gut microbiota
lokal late-onset sepsis
lokal metabolome
1000 Fachgruppe
  1. Gesundheitswesen |
  2. Ernährungswissenschaften |
  3. Medizin |
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/creator/RW1ibGV0b24sIE5pY2hvbGFzIEQu|https://frl.publisso.de/adhoc/creator/QmVycmluZ3RvbiwgSmFuZXQgRS4=|https://frl.publisso.de/adhoc/creator/RG9ybGluZywgSm9u|https://frl.publisso.de/adhoc/creator/RXdlciwgQW5kcmV3IEsu|https://frl.publisso.de/adhoc/creator/SnVzemN6YWssIEVkbXVuZA==|https://frl.publisso.de/adhoc/creator/S2lyYnksIEpvaG4gQS4=|https://frl.publisso.de/adhoc/creator/TGFtYiwgQ2hyaXN0b3BoZXIgQS4=|https://frl.publisso.de/adhoc/creator/TGFueW9uLCBDbGFyZSBWLg==|https://frl.publisso.de/adhoc/creator/TWNHdWlyZSwgV2lsbGlhbQ==|https://frl.publisso.de/adhoc/creator/UHJvYmVydCwgQ2hyaXN0b3BoZXIgUy4=|https://frl.publisso.de/adhoc/creator/UnVzaHRvbiwgU3RlcGhlbiBQLg==|https://frl.publisso.de/adhoc/creator/U2hpcmxleSwgTWFyayBELg==|https://frl.publisso.de/adhoc/creator/U3Rld2FydCwgQ2hyaXN0b3BoZXIgSi4=|https://frl.publisso.de/adhoc/creator/Q3VtbWluZ3MsIFN0ZXBoZW4gUC4=
1000 Label
1000 Förderer
  1. UK National Institute for Health Research (UK NIHR)
1000 Fördernummer
  1. 13/122/02
1000 Förderprogramm
  1. Health Technology Assessment programme; Efficacy and Mechanistic Evaluation Programme (EME)
1000 Dateien
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6409577.rdf
1000 Erstellt am 2018-08-23T16:16:19.638+0200
1000 Erstellt von 122
1000 beschreibt frl:6409577
1000 Bearbeitet von 122
1000 Zuletzt bearbeitet 2020-01-31T00:21:23.792+0100
1000 Objekt bearb. Thu Aug 23 16:17:14 CEST 2018
1000 Vgl. frl:6409577
1000 Oai Id
  1. oai:frl.publisso.de:frl:6409577 |
1000 Sichtbarkeit Metadaten public
1000 Sichtbarkeit Daten public
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