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In vitro assessment of iron availability from commercial Young Child Formulae supplemented with prebiotics

PURPOSE: Iron is essential for development and growth in young children; unfortunately, iron deficiency (ID) is a significant public health problem in this population. Young Child Formulae (YCF), milk-derived products fortified with iron and ascorbic acid (AA, an enhancer of iron absorption) may be...

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Autores principales: Christides, Tatiana, Ganis, Julia Clark, Sharp, Paul Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845627/
https://www.ncbi.nlm.nih.gov/pubmed/27942845
http://dx.doi.org/10.1007/s00394-016-1353-3
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author Christides, Tatiana
Ganis, Julia Clark
Sharp, Paul Anthony
author_facet Christides, Tatiana
Ganis, Julia Clark
Sharp, Paul Anthony
author_sort Christides, Tatiana
collection PubMed
description PURPOSE: Iron is essential for development and growth in young children; unfortunately, iron deficiency (ID) is a significant public health problem in this population. Young Child Formulae (YCF), milk-derived products fortified with iron and ascorbic acid (AA, an enhancer of iron absorption) may be good sources of iron to help prevent ID. Furthermore, some YCF are supplemented with prebiotics, non-digestible carbohydrates suggested to enhance iron bioavailability. The aim of our study was to evaluate iron bioavailability of YCF relative to prebiotic and AA concentrations. We hypothesised that YCF with the highest levels of prebiotics and AA would have the most bioavailable iron. METHODS: We used the in vitro digestion/Caco-2 cell model to measure iron bioavailability from 4 commercially available YCF with approximately equal amounts of iron, but varying amounts of: AA and the prebiotics fructo- and galacto-oligosaccharides. Caco-2 cell ferritin formation was used as a surrogate marker for iron bioavailability. RESULTS: The YCF with the highest concentration of prebiotics and AA had the highest iron bioavailability; conversely, the YCF with the lowest concentration of prebiotics and AA had the lowest. After the addition of exogenous prebiotics, so that all tested YCF had equivalent amounts, there was no longer a significant difference between YCF iron bioavailability. CONCLUSION: Our results suggest that ascorbic acid and prebiotics in YCF improve iron bioavailability. Ensuring that iron is delivered in a bioavailable form would improve the nutritional benefits of YCF in relation to ID/IDA amongst young children; therefore, further exploration of our findings in vivo is warranted.
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spelling pubmed-58456272018-03-20 In vitro assessment of iron availability from commercial Young Child Formulae supplemented with prebiotics Christides, Tatiana Ganis, Julia Clark Sharp, Paul Anthony Eur J Nutr Original Contribution PURPOSE: Iron is essential for development and growth in young children; unfortunately, iron deficiency (ID) is a significant public health problem in this population. Young Child Formulae (YCF), milk-derived products fortified with iron and ascorbic acid (AA, an enhancer of iron absorption) may be good sources of iron to help prevent ID. Furthermore, some YCF are supplemented with prebiotics, non-digestible carbohydrates suggested to enhance iron bioavailability. The aim of our study was to evaluate iron bioavailability of YCF relative to prebiotic and AA concentrations. We hypothesised that YCF with the highest levels of prebiotics and AA would have the most bioavailable iron. METHODS: We used the in vitro digestion/Caco-2 cell model to measure iron bioavailability from 4 commercially available YCF with approximately equal amounts of iron, but varying amounts of: AA and the prebiotics fructo- and galacto-oligosaccharides. Caco-2 cell ferritin formation was used as a surrogate marker for iron bioavailability. RESULTS: The YCF with the highest concentration of prebiotics and AA had the highest iron bioavailability; conversely, the YCF with the lowest concentration of prebiotics and AA had the lowest. After the addition of exogenous prebiotics, so that all tested YCF had equivalent amounts, there was no longer a significant difference between YCF iron bioavailability. CONCLUSION: Our results suggest that ascorbic acid and prebiotics in YCF improve iron bioavailability. Ensuring that iron is delivered in a bioavailable form would improve the nutritional benefits of YCF in relation to ID/IDA amongst young children; therefore, further exploration of our findings in vivo is warranted. Springer Berlin Heidelberg 2016-12-09 2018 /pmc/articles/PMC5845627/ /pubmed/27942845 http://dx.doi.org/10.1007/s00394-016-1353-3 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Contribution
Christides, Tatiana
Ganis, Julia Clark
Sharp, Paul Anthony
In vitro assessment of iron availability from commercial Young Child Formulae supplemented with prebiotics
title In vitro assessment of iron availability from commercial Young Child Formulae supplemented with prebiotics
title_full In vitro assessment of iron availability from commercial Young Child Formulae supplemented with prebiotics
title_fullStr In vitro assessment of iron availability from commercial Young Child Formulae supplemented with prebiotics
title_full_unstemmed In vitro assessment of iron availability from commercial Young Child Formulae supplemented with prebiotics
title_short In vitro assessment of iron availability from commercial Young Child Formulae supplemented with prebiotics
title_sort in vitro assessment of iron availability from commercial young child formulae supplemented with prebiotics
topic Original Contribution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845627/
https://www.ncbi.nlm.nih.gov/pubmed/27942845
http://dx.doi.org/10.1007/s00394-016-1353-3
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