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Overweight impairs efficacy of iron supplementation in iron-deficient South African children: a randomized controlled
J Baumgartner1, C M Smuts, I Aeberli
1Centre of Exellence for Nutrition (CEN), North-West University, Potchefstroom, South Africa. jeannine.baumgartner@gmail.com
Insights
Overweight children with iron deficiency (ID) are at higher risk of remaining iron deficient after supplementation. Higher body mass index (BMI) in children with ID may reduce iron absorption, impacting anemia control efforts.
Area of Science:
- Pediatric Nutrition
- Nutritional Biochemistry
- Public Health
Background:
- Countries undergoing nutrition transition often face high rates of iron deficiency (ID) and overweight (OW).
- Overweight status in children may exacerbate ID, potentially due to inflammation hindering iron absorption.
Purpose of the Study:
- To determine if weight status influences the effectiveness of oral iron supplementation in South African children with ID.
- Investigate the predictive role of body mass index-for-age z-scores (BAZ) on treatment response.
Main Methods:
- A placebo-controlled trial involving 321 children aged 6-11 years with ID, with 28% classified as OW or obese.
- Oral iron supplementation (50 mg, 4x weekly for 8.5 months) or placebo was administered.
- Measurements included BMI-for-age z-scores (BAZ), hepcidin, hemoglobin, serum ferritin (SF), transferrin receptor (TfR), zinc protoporphyrin (ZnPP), and C-reactive protein (CRP). Body iron was calculated using the SF to TfR ratio.
Main Results:
- Higher BAZ correlated with increased C-reactive protein (CRP) and hepcidin levels at baseline.
- Children with normal weight who received iron showed significantly lower TfR levels compared to overweight children receiving iron or placebo.
- Increased BAZ predicted higher TfR and lower body iron at endpoint, and a higher likelihood of remaining iron deficient.
Conclusions:
- Children with higher BAZ have a doubled risk of persistent ID post-supplementation, likely due to elevated hepcidin reducing iron absorption.
- The rising prevalence of overweight in developing nations may impede efforts to combat anemia in vulnerable populations.
- Clinical trial registered with ClinicalTrials.gov (NCT01092377).
Background:
Many countries in the nutrition transition have high rates of iron deficiency (ID) and overweight (OW). ID is more common in OW children; this may be due to adiposity-related inflammation reducing iron absorption.
Objective:
We investigated whether weight status predicts response to oral iron supplementation in ID South African children.
Design:
A placebo-controlled trial of oral iron supplementation (50 mg, 4 × weeks for 8.5 months) was done in ID 6- to 11-year-old children (n=321); 28% were OW or obese. BMI-for-age z-scores (BAZ), hepcidin (in a sub-sample), hemoglobin, serum ferritin (SF), transferrin receptor (TfR), zinc protoporphyrin (ZnPP) and C-reactive protein (CRP) were measured; body iron was calculated from the SF to TfR ratio.
Results:
At baseline, BAZ correlated with CRP (r=0.201, P<0.001) and CRP correlated with hepcidin (r=0.384, P<0.001). Normal weight children supplemented with iron had significantly lower TfR concentrations at endpoint than the OW children supplemented with iron and the children receiving placebo. Higher BAZ predicted higher TfR (β=0.232, P<0.001) and lower body iron (β=-0.090, P=0.016) at endpoint, and increased the odds ratio (OR) for remaining ID at endpoint in both the iron and placebo groups (iron: OR 2.31, 95% CI: 1.13, 4.73; placebo: OR 1.78, 95% CI: 1.09, 2.91). In the children supplemented with iron, baseline hepcidin and BAZ were significant predictors of endpoint TfR, with a trend towards a hepcidin × BAZ interaction (P=0.058).
Conclusion:
South African children with high BAZ have a two-fold higher risk of remaining ID after iron supplementation. This may be due to their higher hepcidin concentrations reducing iron absorption. Thus, the current surge in OW in rapidly developing countries may undercut efforts to control anemia in vulnerable groups. The trial is registered at clinicaltrials.gov as NCT01092377.
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