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Updated: Nov 12, 2025

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Published on: August 24, 2011
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.
Objectives:
This systematic review and meta-analysis study aimed to estimate the overall prevalence of Glucose-6-phosphate dehydrogenase (G6PD) deficiency in neonates with jaundice who were admitted to hospitals in Iran.
Materials And Methods:
In this systematic review and meta-analysis, we searched PubMed/Medline, Scopus, ISI Web of Sciences, and Iranian Local databases up to December 2019.We calculated Prevalence and 95% Confidence Interval (95% CI) of G6PD deficiency as summary measures. We conducted subgroup analysis based on the sex and quality of studies, while meta-regression were applied for investigating the effect of years of studies and years of publication on the pooled prevalence. We applied sensitivity analysis to investigate the effect of excluding each study on the pooled prevalence estimation.
Results:
The total sample size was 9799 people. The pooled prevalence of G6PD deficiency among neonates with jaundice in Iran was 7.0% (95% CI: 5.5-8.5%). The results of subgroup analysis showed that, pooled prevalence of G6PD deficiency among male neonate (12.1%, 95%CI: 7.6-16.7%) was more prevalent that female (3.00%, 95%CI: 1.1-4.9%). Based on the sensitivity analysis, lower and higher pooled prevalence of G6PD deficiency was observed 5.8% (95%CI: 4.7-6.9%) and 7.3% (95%CI: 5.7-8.8%) respectively by excluding each study.
Conclusion:
The overall prevalence of G6PD deficiency was 7% in Iranian neonates with Jaundice. Prevalence was high in male and early hours of life. We recommend screening test for G6PD deficiency in neonates to prevent its complications.
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