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Glucose-6-phosphate dehydrogenase deficiency among neonates with jaundice in Africa; systematic review and
Woldeteklehaymanot Kassahun1, Abayneh Tunta2, Atitegeb Abera3
1Department of Medical Laboratory Sciences, College of Health Sciences, Woldia University, Po Box, 400, Woldia, Ethiopia.
Insights
Glucose-6-phosphate dehydrogenase (G6PD) deficiency affects nearly a quarter of African neonates with jaundice. Early screening for this genetic disorder is recommended due to its significant prevalence in the region.
Area of Science:
- Medical Genetics
- Neonatal Medicine
- Public Health
Background:
- Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common genetic enzyme disorder.
- It disproportionately affects populations in Africa, Asia, and the Mediterranean.
- Neonatal jaundice is a frequent clinical presentation in newborns.
Purpose of the Study:
- To determine the prevalence of G6PD deficiency in African neonates presenting with jaundice.
- To synthesize existing data on G6PD deficiency in this specific demographic.
Main Methods:
- A systematic literature search was conducted across major scientific databases.
- Ten studies involving 1555 neonates were included and quality assessed using JBI criteria.
- Meta-analysis with random effects modeling was employed to calculate pooled prevalence and assess heterogeneity.
Main Results:
- The pooled prevalence of G6PD deficiency among jaundiced neonates in Africa was 24.60%.
- Significant heterogeneity was observed across studies (I² = 100%).
- Prevalence varied widely by country, with Nigeria reporting 49.67% and South Africa 3.14%.
Conclusions:
- G6PD deficiency is a significant contributing factor to neonatal jaundice in Africa.
- Further research into regional predisposing factors is warranted.
- Screening and diagnostic testing for G6PD deficiency in neonates with jaundice should be considered.
Background:
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a genetic disorder caused by a structural abnormality in the enzyme. G6PD deficiency is most prevalent among African, Asian, and Mediterranean people. This study aimed to investigate how prevalent G6PD deficiency is in African neonates with jaundice.
Methods:
The public sources, such as PubMed, Science Direct, Google Scholar, and Africa Journal Online were searched for articles that reported the prevalence of G6PD deficiency published before March 21st, 2022. The Joanna Briggs Institute's (JBI) critical assessment checklist was used to evaluate the quality of individual studies. STATA-17 was used to do the statistical analysis. The pooled prevalence of G6PD deficiency in neonates with jaundice in Africa was calculated using a forest plot and a random effects model. I2 statistics and Galbraith plots were used to assess heterogeneity. Publication bias was assessed using a funnel plot and Egger's statistical test.
Results:
Ten studies involving 1555 neonates with jaundice were involved in the study. G6PD deficiency was prevalent in 24.60% of African neonates with jaundice (95% CI:12.47-36.74) with considerable heterogeneity (I2 = 100%). Nigerian neonates with jaundice had the highest G6PD deficiency (49.67%), whereas South Africans had the lowest (3.14%).
Conclusion:
G6PD deficiency has been implicated in a significant portion of African neonates with jaundice, notwithstanding the need for greater research on predisposing variables from other countries. Therefore, it should be thought of performing screening and diagnostic laboratory tests for G6PD deficiency.
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