Journal article
A double blind randomised controlled trial comparing standard dose of iron supplementation for pregnant women with two screen-and-treat approaches using hepcidin as a biomarker for ready and safe to receive iron
A Bah, R Wegmuller, C Cerami, L Kendall, SR Pasricha, SE Moore, AM Prentice
BMC Pregnancy and Childbirth | BMC | Published : 2016
Abstract
Background: Until recently, WHO recommended daily iron supplementation for all pregnant women (60 mg/d iron combined with 400ug/d folic acid) where anaemia rates exceeded 40 %. Recent studies indicate that this may pose a risk to pregnant women. Therefore, there is a need to explore screen-and-treat options to minimise iron exposure during pregnancy using an overall lower dosage of iron that would achieve equivalent results as being currently recommended by the WHO. However, there is a lack of agreement on how to best assess iron deficiency when infections are prevalent. Here, we test the use of hepcidin a peptide hormone and key regulator of iron metabolism, as a potential index for 'safe a..
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Awarded by Medical Research Council
Funding Acknowledgements
The trial will not be possible without the funding provided by the Bill and Melinda Gates Foundation to the MRC-ING. The trial is also supported by the UK MRC and the UK Department for International Development (DFID) under the MRC/DFID Concordant agreement. We appreciate the valuable contribution of Momodou W. Jallow and Ebrima Ceesay for analysing the blood samples for the determination of the hepcidin cut-off point used in this trial.