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Serum hepcidin in infants born after 32 to 37 wk of gestational age
Lieke Uijterschout1, Magnus Domellöf2, Staffan K Berglund2
1Department of Pediatrics, OLVG, Amsterdam, the Netherlands.
Insights
Hepcidin levels decrease in late preterm infants during the first four months of life. Lower hepcidin indicates iron deficiency (ID) in infants, serving as an early diagnostic marker.
Area of Science:
- Neonatal Medicine
- Pediatric Hematology
- Biochemistry
Background:
- Preterm infants face a high risk of iron deficiency (ID).
- Hepcidin is a potential biomarker for ID in preterm infants, complementing ferritin levels.
Purpose of the Study:
- To investigate serum hepcidin concentrations in late preterm infants.
- To evaluate hepcidin as an early indicator of iron deficiency in this population.
Main Methods:
- Prospective observational study involving 111 late preterm infants (32+0 to 36+6 weeks gestational age).
- Serum hepcidin levels were analyzed during the first four months of life.
- Comparison of hepcidin concentrations between infants with and without ID.
Main Results:
- Hepcidin concentrations naturally decreased over the first four months of life.
- Infants with ID exhibited significantly lower hepcidin levels compared to those without ID.
- Early detection of ID was possible with hepcidin at 1.5 months, while ferritin changes were noted at 1 week.
Conclusions:
- The decrease in hepcidin and ferritin concentrations is a physiological response to increase iron availability in late preterm infants.
- Hepcidin is a valuable early marker for identifying iron deficiency in this cohort.
- While hepcidin is a useful early indicator, it does not offer additional diagnostic value beyond ferritin for ID.
Background:
Preterm infants are at risk of iron deficiency (ID). Hepcidin has been suggested as a good additional indicator of ID in preterm infants, next to ferritin.
Methods:
In a prospective observational study, we analyzed serum hepcidin in 111 infants born after 32+0 to 36+6 wk gestational age during the first 4 mo of life.
Results:
Hepcidin concentrations decreased during the first 4 mo of life, and concentrations were lower in infants with ID compared to those without ID. Infants who developed ID at the age of 4 mo had already significantly lower levels of hepcidin at 1.5 mo of age, while ferritin was already significantly lower at the age of 1 wk.
Conclusion:
Hepcidin concentrations of late preterm infants decrease during the first 4 mo of life. This decrease, which parallels a decrease of ferritin concentration, we interpret as a physiological response, aiming to increase iron availability. Hepcidin concentrations are lower in infants with ID compared with those without ID, with a notable change already observed at 1.5 mo of age. Hepcidin can be used as an early marker of ID, although an additive value of hepcidin over ferritin in the diagnosis of ID is not present.
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