Prevalence of G6PD deficiency in Iranian neonates with jaundice: a systematic review and meta-analysis

Maryam Javadi1,2, Somayeh Deravi2, Shabnam Zarei2

  • 1Children Growth Research Center, Research Institute for Prevention of Non-Communicable Diseases, Qazvin University of Medical Sciences, Qazvin, Iran.

Insights

The overall prevalence of Glucose-6-phosphate dehydrogenase (G6PD) deficiency in Iranian neonates with jaundice is 7%. This G6PD deficiency is more common in males and necessitates screening to prevent complications.

Area of Science:

  • Medical Research
  • Neonatal Health
  • Genetic Disorders

Background:

  • Neonatal jaundice is a common condition, and Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a significant underlying cause.
  • Estimating the prevalence of G6PD deficiency in neonates with jaundice in Iran is crucial for public health planning and intervention.

Approach:

  • A systematic review and meta-analysis was conducted, searching major scientific databases up to December 2019.
  • Prevalence and 95% Confidence Intervals (CI) were calculated as summary measures.
  • Subgroup, meta-regression, and sensitivity analyses were performed to explore variations and robustness of the findings.

Key Points:

  • The pooled prevalence of G6PD deficiency among neonates with jaundice in Iran was found to be 7.0% (95% CI: 5.5-8.5%).
  • Prevalence was significantly higher in male neonates (12.1%) compared to female neonates (3.00%).
  • Sensitivity analyses confirmed the robustness of the pooled prevalence estimates.

Conclusions:

  • The study confirms a 7% prevalence of G6PD deficiency in Iranian neonates presenting with jaundice.
  • Higher prevalence in males and early hours of life suggests specific risk groups.
  • Routine screening for G6PD deficiency in neonates is recommended to mitigate potential complications.
Abstract

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