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Hemoglobin Response to a Low-Iron Dose in Infantile Anemia
Masahiko Kimura1, Takeshi Taketani2
1Pediatrics, Kimura Children and Family Clinic, Izumo, JPN.
Insights
A lower iron dose of 1 mg/kg/day proved as effective as the standard 15 mg/day dose for treating infantile anemia. This finding suggests lower therapeutic iron doses may safely manage iron-deficiency anemia in infants.
Area of Science:
- Pediatrics
- Hematology
- Nutritional Science
Background:
- Iron-deficiency anemia (IDA) is prevalent in exclusively breastfed infants over six months.
- Standard iron doses (3-6 mg/kg/day) risk adverse effects like gut dysbiosis and oxidative stress.
- Lower iron doses show promise for IDA treatment in adults.
Purpose of the Study:
- To evaluate the hemoglobin (Hb) response to a lower iron dose in infants with anemia.
- To compare the efficacy of 1 mg/kg/day iron versus a fixed 15 mg/day dose.
Main Methods:
- Retrospective analysis of exclusively breastfed infants aged 9-10 months screened for anemia.
- Collected clinical data and performed complete blood counts (CBC).
- Compared Hb response after four weeks between a reference group (15 mg/day) and a low-dose group (1 mg/kg/day).
Main Results:
- The fixed 15 mg/day dose averaged 1.8 mg/kg/day.
- Both groups showed similar median Hb increases (1.6 g/dL vs. 1.5 g/dL).
- 70% of infants in the low-dose group achieved Hb response, with a median increase of 2.2 g/dL for those meeting the WHO anemia definition (Hb < 10.5 g/dL).
Conclusions:
- An iron dose of 1 mg/kg/day is as effective as 15 mg/day for improving Hb response in infants.
- Lower iron doses may effectively manage IDA while potentially reducing risks associated with higher doses.
- Findings support exploring reduced therapeutic iron doses for infantile anemia.
Introduction:
Iron-deficiency anemia (IDA) is common during infancy, especially among infants exclusively breastfed after six months of age. The recommended therapeutic iron dose is 3-6 mg/kg/day; however, excessive iron load can be harmful due to alteration of the gut microbiome and oxidative stress to the developing organs. Lower doses of iron have shown efficacy in treating IDA in adults. This retrospective study evaluated the hemoglobin (Hb) response to a lower iron dose in infantile anemia.
Methods:
During health checkups for 9- to 10-month-old infants, anemia screening was conducted for those who were exclusively breastfed. Clinical parameters, including birth date, gestational age, birth weight, and body weight at the start of iron supplementation, were recorded. Venous blood samples were collected for a complete blood count (CBC). Infants with either Hb levels below 11.0 g/dL or mean corpuscular volume below 70 fL received a therapeutic iron trial. From March 2016 to November 2018, a fixed dose of elemental iron (soluble ferric pyrophosphate) 15 mg/day was administered (reference group), and from November 2018 to December 2023, a dose of 1 mg/kg/day was given (low-dose group). CBC measurements were repeated after four weeks, and Hb responses were compared between the two regimens.
Results:
A total of 26 children in the reference group and 27 in the low-dose group were finally analyzed. The fixed 15 mg/day dose in the reference group corresponded to 1.8 (1.6-1.9) (median (interquartile range) mg/kg/day). Baseline clinical variables showed no statistically significant differences between the two groups. The median Hb increase was 1.6 g/dL and 1.5 g/dL, with 69% (18/26) and 70% (19/27) of children achieving an Hb level ≥ 1 g/dL, in the reference and low-dose groups, respectively. All 15 children (15/27, 56%) in the low-dose group, who met the new WHO anemia definition at the age of 6-23 months of Hb < 10.5 g/dL, had an Hb response ≥ 1.0 g/dL, with a median Hb response of 2.2 g/dL.
Conclusion:
An iron dose of 1 mg/kg/day was as effective as 15 mg/day (median: 1.8 mg/kg/day) in the Hb response. In all children with Hb < 10.5 g/dL, the iron dose of 1 mg/kg/day showed substantial Hb responses. These findings suggest that therapeutic iron doses lower than conventional recommendations may be effective for managing IDA and mitigating the harmful effects.
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