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Growth in non-anemic infants supplemented with different prophylactic iron doses
Danielle G Silva1, Sylvia do C C Franceschini, Dirce M Sigulem
1Universidade Federal de São Paulo - Escola Paulista de Medicina (UNIFESP-EPM), São Paulo, SP, Brazil. daniellegoes@ufs.br
Insights
Different prophylactic iron doses did not impact the growth or nutritional status of non-anemic infants. This study found no significant differences in weight, length, or morbidity across various iron supplementation regimens.
Area of Science:
- Pediatric Nutrition
- Iron Metabolism
- Infant Growth and Development
Background:
- Iron deficiency is a global health concern, impacting infant development.
- Prophylactic iron supplementation is common, but optimal dosing for non-anemic infants remains debated.
- Understanding the effects of different iron doses is crucial for public health guidelines.
Purpose of the Study:
- To evaluate the impact of varying prophylactic iron doses on the growth and nutritional status of non-anemic infants.
- To compare the efficacy of daily versus weekly iron supplementation regimens.
- To assess the influence of iron dosing on infant morbidity.
Main Methods:
- A prospective randomized study involving 114 non-anemic infants aged 5.0 to 6.9 months.
- Infants were allocated to receive iron (ferrous sulfate) at 1 mg/kg/day, 2 mg/kg/day, or 25 mg/week for 16 weeks.
- Anthropometric measurements (weight, length) and World Health Organization (WHO) z-scores were used to assess nutritional status; morbidity was monitored monthly.
Main Results:
- Baseline nutritional status and daily nutrient intake were similar across all groups.
- No statistically significant differences were observed in weight gain, length gain, or changes in anthropometric indices among the iron-supplemented groups.
- The incidence and duration of morbidity episodes did not differ significantly between the groups.
Conclusions:
- Prophylactic iron supplementation with different doses (1 mg/kg/day, 2 mg/kg/day, 25 mg/week) showed no differential effects on the growth and nutritional status of non-anemic infants.
- Current prophylactic iron dosing strategies do not appear to significantly alter key growth parameters or health outcomes in this population.
- Further research may explore long-term implications or specific subpopulations.
Objective:
To compare the effects of different prophylactic iron doses on the growth and nutritional status of non-anemic infants.
Methods:
Prospective randomized study. Infants aged 5.0 to 6.9 months who met the inclusion criteria and showed capillary hemoglobin >or= 11 g/dL were randomly allocated into three groups who received the following prophylactic doses of iron supplement (ferrous sulfate): 1 mg/kg/day (n = 39); 2 mg/kg/day (n = 36); and 25 mg/week (n = 39). This supplementation was given during 16 weeks. Both weight and length were measured. The nutritional status was evaluated by comparing z scores for weight/age, length/age and weight/length based on the World Health Organization (2006) references. Morbidity information was collected during monthly visits.
Results:
The groups showed similar nutritional status before supplementation. There were no differences in daily nutrient intake among groups. During the study, weight and length gain, and increments in anthropometric indices did not differ statistically among supplemented groups. The occurrence and duration of morbidity episodes did not differ statistically among groups. In general, improvements were observed in both weight/age and weight/length indices in the population under study, whereas length/age showed no differences before and after supplementation.
Conclusion:
Different prophylactic iron doses had no different effects on the growth and nutritional status of non-anemic infants.
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