University of Leicester
Browse

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

Download (443.01 kB)
journal contribution
posted on 2019-09-03, 11:24 authored by Tatiana Christides, Julia Clark Ganis, Paul Anthony Sharp
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.

Funding

The Faculty of Engineering and Science at the University of Greenwich, and the Diabetes and Nutritional Sciences Division at King’s College London, supported this work. We thank David Scott Ganis for assistance with statistical and numerical analysis.

History

Citation

European Journal of Nutrition, 2018, 57 (2), pp. 669-678

Author affiliation

/Organisation/COLLEGE OF LIFE SCIENCES/School of Medicine

Version

  • VoR (Version of Record)

Published in

European Journal of Nutrition

Publisher

Springer (part of Springer Nature)

eissn

1436-6215

Acceptance date

2016-11-29

Copyright date

2016

Available date

2019-09-03

Publisher version

https://link.springer.com/article/10.1007/s00394-016-1353-3

Language

en