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Updated: Jul 18, 2025

Biochemical Measurement of Neonatal Hypoxia
Published on: August 24, 2011
Do Lower Levels of Fetal Hemoglobin in Preterm Infants Relate to Oxidative Stress?
Laura Torrejón-Rodríguez1, Anna Parra-Llorca2, Alejandro Pinilla-González1
1Neonatal Research Group, Health Research Institute La Fe, Valencia, Spain.
Insights
Preterm infants receiving adult blood transfusions experience a drop in fetal hemoglobin (HbF). Lower HbF levels correlate with increased oxidative stress biomarkers in these vulnerable newborns.
Area of Science:
- Neonatal physiology
- Hematology
- Oxidative stress research
Background:
- Fetal hemoglobin (HbF) facilitates oxygen transfer for fetal development.
- Preterm infants often receive adult blood transfusions, reducing HbF levels.
- This reduction may lead to increased oxygen delivery and a pro-oxidant state.
Discussion:
- This study compared oxidative stress biomarkers in preterm infants (<32 weeks' gestation) based on HbF levels.
- Urine samples from 56 infants were analyzed.
- Statistical analysis (Wilcoxon rank sum test) revealed significant differences.
Key Insights:
- Preterm neonates with lower circulating fetal hemoglobin (HbF) exhibited significantly higher levels of oxidative stress biomarkers.
- This suggests a potential protective role for HbF against oxidative damage in the newborn period.
- Findings indicate a link between HbF levels and oxidative stress in preterm infants.
Outlook:
- Further research is warranted to confirm HbF's protective role against free radical-associated conditions in neonates.
- Investigating interventions to maintain HbF levels could mitigate oxidative stress in preterm infants.
- Exploring the precise mechanisms by which HbF influences oxidative stress is a future direction.
Abstract:
Fetal hemoglobin (HbF) has a higher affinity to oxygen than adult hemoglobin, allowing for a slower oxygen transfer to peripheral tissue, creating a microenvironment conducive to adequate fetal development in utero. However, most preterm infants receive packed red blood cell transfusions from adult donors leading to a drastic nonphysiological descent of circulating HbF. We hypothesized that this drop could enhance oxygen delivery to peripheral tissues generating a hyperoxic pro-oxidant environment. To investigate this, we assessed differences in oxidative stress biomarkers determined in urine samples in a cohort of 56 preterm infants born <32 weeks' gestation. Median oxidative stress biomarkers were compared between patients with circulating HbF above or below median HbF levels using Wilcoxon rank sum test. Oxidative stress biomarkers were significantly higher in the group of patients with lower levels of HbF. This study provides the initial evidence indicating elevated levels of oxidative stress biomarkers in preterm neonates with lower HbF levels. Based on the results, we hypothesize that HbF may contribute to preventing free radical-associated conditions during the newborn period. Antioxid. Redox Signal. 40, 453-459.
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