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Urinary Metabolomic Profile of Preterm Infants Receiving Human Milk with Either Bovine or Donkey Milk-Based Fortifiers

Fortification of human milk (HM) for preterm and very low-birth weight (VLBW) infants is a standard practice in most neonatal intensive care units. The optimal fortification strategy and the most suitable protein source for achieving better tolerance and growth rates for fortified infants are still...

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Autores principales: Giribaldi, Marzia, Peila, Chiara, Coscia, Alessandra, Cavallarin, Laura, Antoniazzi, Sara, Corbu, Sara, Maiocco, Giulia, Sottemano, Stefano, Cresi, Francesco, Moro, Guido E., Bertino, Enrico, Fanos, Vassilios, Cesare Marincola, Flaminia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468788/
https://www.ncbi.nlm.nih.gov/pubmed/32727157
http://dx.doi.org/10.3390/nu12082247
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author Giribaldi, Marzia
Peila, Chiara
Coscia, Alessandra
Cavallarin, Laura
Antoniazzi, Sara
Corbu, Sara
Maiocco, Giulia
Sottemano, Stefano
Cresi, Francesco
Moro, Guido E.
Bertino, Enrico
Fanos, Vassilios
Cesare Marincola, Flaminia
author_facet Giribaldi, Marzia
Peila, Chiara
Coscia, Alessandra
Cavallarin, Laura
Antoniazzi, Sara
Corbu, Sara
Maiocco, Giulia
Sottemano, Stefano
Cresi, Francesco
Moro, Guido E.
Bertino, Enrico
Fanos, Vassilios
Cesare Marincola, Flaminia
author_sort Giribaldi, Marzia
collection PubMed
description Fortification of human milk (HM) for preterm and very low-birth weight (VLBW) infants is a standard practice in most neonatal intensive care units. The optimal fortification strategy and the most suitable protein source for achieving better tolerance and growth rates for fortified infants are still being investigated. In a previous clinical trial, preterm and VLBW infants receiving supplementation of HM with experimental donkey milk-based fortifiers (D-HMF) showed decreased signs of feeding intolerance, including feeding interruptions, bilious gastric residuals and vomiting, with respect to infants receiving bovine milk-based fortifiers (B-HMF). In the present ancillary study, the urinary metabolome of infants fed B-HMF (n = 27) and D-HMF (n = 27) for 21 days was analyzed by (1)H NMR spectroscopy at the beginning (T0) and at the end (T1) of the observation period. Results showed that most temporal changes in the metabolic responses were common in the two groups, providing indications of postnatal adaptation. The significantly higher excretion of galactose in D-HMF and of carnitine, choline, lysine and leucine in B-HMF at T1 were likely due to different formulations. In conclusion, isocaloric and isoproteic HM fortification may result in different metabolic patterns, as a consequence of the different quality of the nutrients provided by the fortifiers.
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spelling pubmed-74687882020-09-04 Urinary Metabolomic Profile of Preterm Infants Receiving Human Milk with Either Bovine or Donkey Milk-Based Fortifiers Giribaldi, Marzia Peila, Chiara Coscia, Alessandra Cavallarin, Laura Antoniazzi, Sara Corbu, Sara Maiocco, Giulia Sottemano, Stefano Cresi, Francesco Moro, Guido E. Bertino, Enrico Fanos, Vassilios Cesare Marincola, Flaminia Nutrients Article Fortification of human milk (HM) for preterm and very low-birth weight (VLBW) infants is a standard practice in most neonatal intensive care units. The optimal fortification strategy and the most suitable protein source for achieving better tolerance and growth rates for fortified infants are still being investigated. In a previous clinical trial, preterm and VLBW infants receiving supplementation of HM with experimental donkey milk-based fortifiers (D-HMF) showed decreased signs of feeding intolerance, including feeding interruptions, bilious gastric residuals and vomiting, with respect to infants receiving bovine milk-based fortifiers (B-HMF). In the present ancillary study, the urinary metabolome of infants fed B-HMF (n = 27) and D-HMF (n = 27) for 21 days was analyzed by (1)H NMR spectroscopy at the beginning (T0) and at the end (T1) of the observation period. Results showed that most temporal changes in the metabolic responses were common in the two groups, providing indications of postnatal adaptation. The significantly higher excretion of galactose in D-HMF and of carnitine, choline, lysine and leucine in B-HMF at T1 were likely due to different formulations. In conclusion, isocaloric and isoproteic HM fortification may result in different metabolic patterns, as a consequence of the different quality of the nutrients provided by the fortifiers. MDPI 2020-07-27 /pmc/articles/PMC7468788/ /pubmed/32727157 http://dx.doi.org/10.3390/nu12082247 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Giribaldi, Marzia
Peila, Chiara
Coscia, Alessandra
Cavallarin, Laura
Antoniazzi, Sara
Corbu, Sara
Maiocco, Giulia
Sottemano, Stefano
Cresi, Francesco
Moro, Guido E.
Bertino, Enrico
Fanos, Vassilios
Cesare Marincola, Flaminia
Urinary Metabolomic Profile of Preterm Infants Receiving Human Milk with Either Bovine or Donkey Milk-Based Fortifiers
title Urinary Metabolomic Profile of Preterm Infants Receiving Human Milk with Either Bovine or Donkey Milk-Based Fortifiers
title_full Urinary Metabolomic Profile of Preterm Infants Receiving Human Milk with Either Bovine or Donkey Milk-Based Fortifiers
title_fullStr Urinary Metabolomic Profile of Preterm Infants Receiving Human Milk with Either Bovine or Donkey Milk-Based Fortifiers
title_full_unstemmed Urinary Metabolomic Profile of Preterm Infants Receiving Human Milk with Either Bovine or Donkey Milk-Based Fortifiers
title_short Urinary Metabolomic Profile of Preterm Infants Receiving Human Milk with Either Bovine or Donkey Milk-Based Fortifiers
title_sort urinary metabolomic profile of preterm infants receiving human milk with either bovine or donkey milk-based fortifiers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468788/
https://www.ncbi.nlm.nih.gov/pubmed/32727157
http://dx.doi.org/10.3390/nu12082247
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