Poor correlation between hemolysis and jaundice in glucose 6-phosphate dehydrogenase-deficient babies

Pediatr Int. 2005 Jun;47(3):258-61. doi: 10.1111/j.1442-200x.2005.02052.x.

Abstract

Background: The role of hemolysis in the pathophysiology of neonatal jaundice (NNJ) in patients with glucose 6-phosphate dehydrogenase (G6PD) deficiency has been questioned recently. The aim of the present study was to determine the contribution of hemolysis to the pathophysiology of jaundice in Malay neonates with G6PD deficiency and NNJ.

Methods: Four groups of babies were included in the study: (i) G6PD deficient with NNJ; (ii) G6PD deficient without NNJ; (iii) G6PD normal with NNJ; and (iv) normal controls. Babies with other known causes of jaundice were excluded from the study. All subjects underwent the following investigations on day 3-5 after birth: hemoglobin level (Hb), serum bilirubin level, carboxyhemoglobin (CO-Hb) concentration, reticulocyte count and full blood picture. The results of the investigations were compared between the groups using SPSS version 11.

Results: Babies with G6PD and jaundice had a similar percentage of CO-Hb to babies with G6PD without NNJ or babies with normal G6PD and NNJ (1.76 +/- 0.40% vs 1.66 +/- 0.31% and 1.67 +/- 0.28%, respectively; P: 0.23 and 0.41, respectively). Total Hb levels and reticulocyte counts were not significantly different between the groups. The blood film showed more (even though not reaching significance) hemolysis in the G6PD patients but results of the blood film were very similar for G6PD patients with and those without NNJ.

Conclusion: Hemolysis is not a main determinant of neonatal jaundice in G6PD-deficient babies.

MeSH terms

  • Bilirubin / blood
  • Carboxyhemoglobin / analysis
  • Case-Control Studies
  • Cross-Sectional Studies
  • Female
  • Glucosephosphate Dehydrogenase Deficiency / blood
  • Glucosephosphate Dehydrogenase Deficiency / physiopathology*
  • Hemoglobins / analysis
  • Hemolysis
  • Humans
  • Infant, Newborn
  • Jaundice, Neonatal / physiopathology*
  • Malaysia
  • Male
  • Reticulocyte Count
  • Risk Factors

Substances

  • Hemoglobins
  • Carboxyhemoglobin
  • Bilirubin