Open access · OA
via OpenAlex
Iron fortification adversely affects the gut microbiome, increases pathogen abundance and induces intestinal inflammation in Kenyan infants
Tanja Jaeggi, Guus A. M. Kortman, Diego Moretti, Christophe Chassard, Penny Holding, Alexandra Dostal, Jos Boekhorst, Harro M. Timmerman, Dorine W. Swinkels, Harold Tjalsma, Jane Njenga, Alice Mwangi, Jane Kvalsvig, Christophe Lacroix, Michael Zimmermann
Gut · 2014 · ▲ 618 citations
Abstract
BACKGROUND: In-home iron fortification for infants in developing countries is recommended for control of anaemia, but low absorption typically results in >80% of the iron passing into the colon. Iron is essential for growth and virulence of many pathogenic enterobacteria. We determined the effect of high and low dose in-home iron fortification on the infant gut microbiome and intestinal inflammation. METHODS: We performed two double-blind randomised controlled trials in 6-month-old Kenyan infants (n=115) consuming home-fortified maize porridge daily for 4 months. In the first, infants received a micronutrient powder (MNP) containing 2.5 mg iron as NaFeEDTA or the MNP without iron. In the second, they received a different MNP containing 12.5 mg iron as ferrous fumarate or the MNP without the iron. The primary outcome was gut microbiome composition analysed by 16S pyrosequencing and targeted real-time PCR (qPCR). Secondary outcomes included faecal calprotectin (marker of intestinal inflammation) and incidence of diarrhoea. We analysed the trials separately and combined. RESULTS: At baseline, 63% of the total microbial 16S rRNA could be assigned to Bifidobacteriaceae but there were high prevalences of pathogens, including Salmonella Clostridium difficile, Clostridium perfringens, and pathogenic Escherichia coli. Using pyrosequencing, +FeMNPs increased enterobacteria, particularly Escherichia/Shigella (p=0.048), the enterobacteria/bifidobacteria ratio (p=0.020), and Clostridium (p=0.030). Most of these effects were confirmed using qPCR; for example, +FeMNPs increased pathogenic E. coli strains (p=0.029). +FeMNPs also increased faecal calprotectin (p=0.002). During the trial, 27.3% of infants in +12.5 mgFeMNP required treatment for diarrhoea versus 8.3% in -12.5 mgFeMNP (p=0.092). There were no study-related serious adverse events in either group. CONCLUSIONS: In this setting, provision of iron-containing MNPs to weaning infants adversely affects the gut microbiome, increasing pathogen abundance and causing intestinal inflammation. TRIAL REGISTRATION NUMBER: NCT01111864.
◌ CITATION ONLY
Full text is not openly licensed for redistribution here. Read it at the source:
Provenance
- Source
- OpenAlex
- DOI
- 10.1136/gutjnl-2014-307720
- Canonical
- link ↗
- Fetched
- 2026-07-29 MST
Cite this
APA
Jaeggi, T., Kortman, G.A.M., Moretti, D., Chassard, C., Holding, P., Dostal, A., Boekhorst, J., Timmerman, H.M., Swinkels, D.W., Tjalsma, H., Njenga, J., Mwangi, A., Kvalsvig, J., Lacroix, C., & Zimmermann, M. (2014). Iron fortification adversely affects the gut microbiome, increases pathogen abundance and induces intestinal inflammation in Kenyan infants. <em>Gut</em>. https://doi.org/10.1136/gutjnl-2014-307720
Vancouver
Jaeggi T, Kortman GAM, Moretti D, Chassard C, Holding P, Dostal A, et al. Iron fortification adversely affects the gut microbiome, increases pathogen abundance and induces intestinal inflammation in Kenyan infants. Gut. 2014. doi:10.1136/gutjnl-2014-307720.
BibTeX
@article{tanja2014Ironfo,
title = {Iron fortification adversely affects the gut microbiome, increases pathogen abundance and induces intestinal inflammation in Kenyan infants},
author = {Tanja Jaeggi and Guus A. M. Kortman and Diego Moretti and Christophe Chassard and Penny Holding and Alexandra Dostal and Jos Boekhorst and Harro M. Timmerman and Dorine W. Swinkels and Harold Tjalsma and Jane Njenga and Alice Mwangi and Jane Kvalsvig and Christophe Lacroix and Michael Zimmermann},
journal = {Gut},
year = {2014},
doi = {10.1136/gutjnl-2014-307720},
}
Research neighborhood
References, citing works, and semantically nearest findings. Click a node to open it.
Related findings
Gut 1996
Open access · OA
Delta 4-3-oxosteroid 5 beta-reductase deficiency: failure of ursodeoxycholic acid treatment and response to chenodeoxycholic acid plus cholic acid.
Immunity & Ageing 2015
Open access · CC-BY
Hormetic effect of rotenone in primary human fibroblasts
BMC Medicine 2020
Open access · CC-BY
Cerebrospinal fluid and plasma biomarkers in individuals at risk for genetic prion disease
Carcinogenesis 2009
Open access · CC-BY
miR-124 and miR-203 are epigenetically silenced tumor-suppressive microRNAs in hepatocellular carcinoma
Dialogues in Clinical Neuroscience 2011
Open access · CC-BY
Of sound mind and body: depression, disease, and accelerated aging
Open Forum Infectious Diseases 2020
Open access · CC-BY