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Evaluating iron status and the risk of anemia in young infants using erythrocyte parameters
Ingrid Kristin Torsvik1, Trond Markestad, Per Magne Ueland
1Department of Pediatrics, Haukeland University Hospital, Bergen, Norway. idto@helse-bergen.no
Insights
Iron supplementation improved iron status in infants, with reticulocyte hemoglobin content (CHr) effectively monitoring iron levels. Early CHr measurements can predict future anemia in at-risk infants.
Area of Science:
- Pediatric Nutrition
- Hematology
- Infant Development
Background:
- Accurate iron status assessment is crucial in young infants due to potential negative impacts of both deficiency and excess on development and health.
- Iron deficiency and overload can adversely affect infant growth, development, and morbidity.
Purpose of the Study:
- To evaluate iron status in infants using erythrocyte parameters, including reticulocyte hemoglobin content (CHr).
- To assess the effectiveness of iron supplementation in infants with low birth weight.
- To identify predictors of anemia in infants.
Main Methods:
- Erythrocyte parameters, including reticulocyte hemoglobin content (CHr), were used to evaluate iron status in infants with birth weight <3,000 g.
- Infant characteristics and blood samples were collected at 6 weeks, 4 months, and 6 months.
- Iron supplementation was recommended for infants with a birth weight ≤2,500 g.
Main Results:
- Iron-supplemented infants showed significantly higher hemoglobin (Hb) and CHr levels at 6 months compared to non-supplemented infants.
- Prolonged exclusive breastfeeding, high weight gain, and male gender were identified as factors predisposing to low iron status at 6 months.
- A CHr cutoff level of 26.9 pg at 4 months predicted anemia at 6 months with high sensitivity.
Conclusions:
- Nonsupplemented infants with birth weights between 2,501-3,000 g exhibited signs of iron-restricted erythropoiesis.
- Reticulocyte hemoglobin content (CHr) proved to be a valuable tool for assessing iron status in infants.
- Further evaluation is needed regarding the necessity of iron supplementation in specific infant risk populations.
Background:
Correct evaluation of iron status is important in young infants because both iron deficiency and excess may have negative effects on development, growth, and morbidity.
Methods:
We evaluated iron status using erythrocyte parameters, including reticulocyte hemoglobin content (CHr) in infants with birth weight <3,000 g (n = 80). Blood samples and infant characteristics were recorded at 6 wk and at 4 and 6 months. Infants with a birth weight ≤2,500 g (n = 36) were recommended for iron supplementation.
Results:
Despite a significantly poorer status at 6 wk, iron-supplemented infants had significantly higher hemoglobin level (Hb): 12.2 (SD = 0.8) g/dl and CHr: 28.3 (SD = 1.4) pg at 6 mo, as compared with nonsupplemented infants, Hb: 11.7 (SD = 1.0) g/dl, P = 0.02 and CHr: 26.5 (SD = 2.5) pg, P < 0.001. Prolonged exclusive breastfeeding, high weight gain, and male gender were the predisposing factors for a low iron status at 6 mo. A CHr cutoff level of 26.9 pg at 4 mo proved to be a sensitive predictor for anemia at 6 mo.
Conclusion:
Signs of an iron-restricted erythropoiesis were observed in nonsupplemented infants (birth weight 2,501-3,000 g), and CHr was a useful tool for evaluating iron status. The need for iron supplementation in certain infant risk populations should be further evaluated.
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