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Fecal amine metabolite analysis before onset of severe necrotizing enterocolitis in preterm infants: a prospective case-control study.
Deianova, N; El Manouni El Hassani, S; Struijs, E A; Jansen, E E W; Bakkali, A; van de Wiel, M A; de Boode, W P; Hulzebos, C V; van Kaam, A H; Kramer, B W; d'Haens, E; Vijlbrief, D C; van Weissenbruch, M M; de Jonge, W J; Benninga, M A; Niemarkt, H J; de Boer, N K H; de Meij, T G J.
Afiliação
  • Deianova N; Department of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Vrije Universiteit, location VUmc, (Room PK-1 Z050), Postbox 7057, 1007 MB, Amsterdam, The Netherlands. n.deianova@amsterdamumc.nl.
  • El Manouni El Hassani S; Department of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Vrije Universiteit, location VUmc, (Room PK-1 Z050), Postbox 7057, 1007 MB, Amsterdam, The Netherlands.
  • Struijs EA; Department of Clinical Chemistry, Amsterdam UMC, Vrije Universiteit, Amsterdam, The Netherlands.
  • Jansen EEW; Department of Clinical Chemistry, Amsterdam UMC, Vrije Universiteit, Amsterdam, The Netherlands.
  • Bakkali A; Department of Clinical Chemistry, Amsterdam UMC, Vrije Universiteit, Amsterdam, The Netherlands.
  • van de Wiel MA; Department of Epidemiology and Data Science, Amsterdam Public Health Research Institute, Amsterdam UMC, Vrije Universiteit, Amsterdam, The Netherlands.
  • de Boode WP; Department of Neonatology, Amalia Children's Hospital, Radboud UMC, Radboud Institute for Health Sciences, Nijmegen, The Netherlands.
  • Hulzebos CV; Division of Neonatology, University Medical Center Groningen, Beatrix Children's Hospital, University of Groningen, Groningen, The Netherlands.
  • van Kaam AH; Department of Neonatology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • Kramer BW; Neonatal Intensive Care Unit, Department of Pediatrics, Maastricht UMC, Maastricht, The Netherlands.
  • d'Haens E; Neonatal Intensive Care Unit, Amalia Children's Center, Isala, Zwolle, The Netherlands.
  • Vijlbrief DC; Neonatal Intensive Care Unit, UMC Utrecht, Wilhelmina Children's Hospital, Utrecht, The Netherlands.
  • van Weissenbruch MM; Department of Neonatology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • de Jonge WJ; Amsterdam Gastroenterology Endocrinology Metabolism (AGEM) Research Institute, Amsterdam UMC, University of Amsterdam, Tytgat Institute for Liver and Intestinal Research, Amsterdam, The Netherlands.
  • Benninga MA; Department of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Vrije Universiteit, Amsterdam, The Netherlands.
  • Niemarkt HJ; Department of Neonatology, Máxima Medical Center, Veldhoven, The Netherlands.
  • de Boer NKH; Department of Gastroenterology and Hepatology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam Gastroenterology Endocrinology Metabolism (AGEM) Research Institute, Amsterdam, The Netherlands.
  • de Meij TGJ; Department of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Vrije Universiteit, location VUmc, (Room PK-1 Z050), Postbox 7057, 1007 MB, Amsterdam, The Netherlands.
Sci Rep ; 12(1): 12310, 2022 07 19.
Article em En | MEDLINE | ID: mdl-35853977
ABSTRACT
Infants developing necrotizing enterocolitis (NEC) have a different metabolomic profile compared to controls. The potential of specific metabolomics, i.e. amino acids and amino alcohols (AAA), as early diagnostic biomarkers for NEC is largely unexplored. In this multicenter prospective case-control study, longitudinally collected fecal samples from preterm infants (born <30 weeks of gestation) from 1-3 days before diagnosis of severe NEC (Bell's stage IIIA/IIIB), were analyzed by targeted high-performance liquid chromatography (HPLC). Control samples were collected from gestational and postnatal age-matched infants. Thirty-one NEC cases (15 NEC IIIA;16 NEC IIIB) with 11 matched controls were included. Preclinical samples of infants with NEC were characterized by five increased essential amino acids-isoleucine, leucine, methionine, phenylalanine and valine. Lysine and ethanolamine ratios were lower prior to NEC, compared to control samples. A multivariate model was rendered based on isoleucine, lysine, ethanolamine, tryptophan and ornithine, modestly discriminating cases from controls (AUC 0.67; p < 0.001). Targeted HPLC pointed to several specific AAA alterations in samples collected 1-3 days before NEC onset, compared to controls. Whether this reflects metabolic alterations and has a role in early biomarker development for NEC, has yet to be elucidated.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Enterocolite Necrosante / Doenças do Recém-Nascido Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Enterocolite Necrosante / Doenças do Recém-Nascido Idioma: En Ano de publicação: 2022 Tipo de documento: Article