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Updated: May 5, 2026

Biochemical Measurement of Neonatal Hypoxia
Published on: August 24, 2011
Is it accurate to separate glucose-6-phosphate dehydrogenase activity in neonatal hyperbilirubinemia as deficient and
Hasan Kilicdag1, Zeynel Gökmen1, Servet Ozkiraz1
1Division of Neonatology, Department of Pediatrics, Faculty of Medicine, Baskent University, Ankara, Turkey.
Insights
Glucose 6-phosphate dehydrogenase (G6PD) activity is crucial for managing severe neonatal hyperbilirubinemia. Lower G6PD levels in infants correlate with longer phototherapy and increased need for exchange transfusions, highlighting the importance of routine G6PD testing.
Area of Science:
- Neonatal Medicine
- Biochemistry
- Pediatric Hematology
Background:
- Severe neonatal hyperbilirubinemia poses risks for neurological dysfunction.
- Glucose 6-phosphate dehydrogenase (G6PD) deficiency can impact bilirubin metabolism.
- Understanding G6PD activity is vital for managing hyperbilirubinemia in newborns.
Purpose of the Study:
- To investigate glucose 6-phosphate dehydrogenase (G6PD) activity in term and late preterm infants with severe neonatal hyperbilirubinemia.
- To explore the relationship between G6PD activity levels and the severity and treatment requirements of hyperbilirubinemia.
- To assess G6PD activity irrespective of deficiency or normal levels.
Main Methods:
- A cohort of 529 term and late preterm infants (≥35 weeks) with severe hyperbilirubinemia was studied.
- Serum samples were analyzed for blood group, direct Coombs' test, complete blood count, bilirubin levels, thyroid-stimulating hormone, and G6PD activity.
- Partial correlation analysis was used to examine the association between G6PD activity and total bilirubin.
Main Results:
- Significant correlation found between hyperbilirubinemia severity and G6PD activity in both male and female neonates.
- Male infants with G6PD <12 U/g Hb and female infants with G6PD <16 U/g Hb required longer phototherapy.
- Decreased G6PD activity was linked to increased phototherapy duration and exchange transfusion necessity.
Conclusions:
- Routine G6PD level screening in hyperbilirubinemic neonates is essential for effective medical management.
- Identifying specific G6PD thresholds (males <12 U/g Hb, females <16 U/g Hb) aids in assessing condition severity.
- Prompt identification and care for severe hyperbilirubinemia in neonates with low G6PD activity are critical to prevent neurological damage.
Background:
The aim of this study was to investigate glucose 6-phosphate dehydrogenase (G6PD) activity in term and late preterm babies with severe neonatal hyperbilirubinemia and its relationship to the severity and treatment of this disorder, regardless of level of G6PD activity (deficient/normal).
Methods:
A total of 529 term and late preterm (≥35 weeks) infants (228 female, 301 male) who were diagnosed with severe hyperbilirubinemia were included in this study. In each case, serum was collected to evaluate blood group, direct Coombs' test, complete blood cell count, total and direct bilirubin, thyroid-stimulating hormone, and G6PD activity. A partial correlation analysis was carried out to assess the relationship between G6PD activity and total bilirubin levels.
Results:
A significant correlation was found between the severity of hyperbilirubinemia and G6PD activity in both males and females. Male neonates who had G6PD levels <12 U/g Hb required more phototherapy time than neonates who had G6PD levels ≥12 U/g Hb; and female neonates who had G6PD levels <16 U/g Hb required more phototherapy time than neonates who had G6PD levels ≥16 U/g Hb (p < 0.0001). When we analyzed only breastfed infants, a significant difference also emerged in both sexes. Decreased G6PD activity was associated with increased phototherapy time and the need for exchange transfusion.
Conclusion:
Routine checks of G6PD level in hyperbilirubinemic neonates are very important in providing proper medical management to prevent bilirubin-induced neurological dysfunction. Appropriate identification of G6PD (<12 U/g Hb for male infants and <16 U/g Hb for female infants) raises awareness of the severity of the condition and the necessity for immediate care of severe hyperbilirubinemic infants.
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