G6PD Enzyme Deficiency in Neonatal Pathologic Hyperbilirubinemia in Yazd

M Pahlavanzadeh1, S Hekmatimoghaddam2, M Teremahi Ardestani3

  • 1Doctor of Laboratory Sciences, School of Paramedicine, Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, Iran.

Insights

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is prevalent in Iranian neonates with jaundice, with 18.1% affected. Early G6PD testing is recommended to prevent complications like hemolysis.

Area of Science:

  • Medical Genetics
  • Neonatology
  • Biochemistry

Background:

  • Glucose-6-phosphate dehydrogenase (G6PD) deficiency affects 7.5% globally, with 10-14.9% prevalence in Iran.
  • This genetic disorder is a significant public health concern, particularly in regions with high carrier rates.

Purpose of the Study:

  • To determine the frequency of G6PD deficiency in jaundiced neonates hospitalized in Yazd, Iran.
  • To assess the association between G6PD deficiency and the severity of neonatal jaundice.

Main Methods:

  • A cohort of 105 icteric neonates was evaluated in Yazd hospitals.
  • G6PD activity was measured using a photometric biochemical assay.
  • Statistical analysis included Student's t-test and Pearson's chi-squared test.

Main Results:

  • 18.1% of neonates (19 out of 105) exhibited G6PD deficiency, with a higher prevalence in boys (29.4%) than girls (7.4%).
  • Jaundice onset occurred within the first week of life in all cases.
  • G6PD-deficient neonates required exchange transfusion significantly more often (31.5%) compared to G6PD-sufficient neonates (4.6%).

Conclusions:

  • The frequency of G6PD deficiency among jaundiced neonates in Yazd is notably high.
  • Given the severity and increased need for intervention, screening all jaundiced neonates for G6PD is recommended.
  • Universal G6PD testing in neonates is advised to prevent severe complications such as favism and drug-induced hemolysis.
Abstract

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