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Updated: Mar 6, 2026

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Published on: August 24, 2011
Comparison of quantitative and qualitative tests for glucose-6-phosphate dehydrogenase deficiency in the neonatal
F Keihanian1,2, S Basirjafari1,3, B Darbandi4
1Guilan University of Medical Sciences, Rasht, Iran.
Insights
Glucose-6-phosphate dehydrogenase (G6PD) deficiency affects 6.6% of newborns in Rasht, Iran. The fluorescent spot test (FST) shows good sensitivity and specificity for screening G6PD deficiency in neonates.
Area of Science:
- Medical Sciences
- Pediatrics
- Genetics
Background:
- Glucose-6-phosphate dehydrogenase (G6PD) deficiency is common in newborns globally.
- Various screening methods are employed for G6PD deficiency detection in neonates.
- Understanding regional prevalence is crucial for public health initiatives.
Purpose of the Study:
- To determine the prevalence of G6PD deficiency in newborns in Rasht, Iran.
- To compare the efficacy of quantitative and qualitative tests for G6PD activity assessment.
- To evaluate the diagnostic performance of the fluorescent spot test (FST).
Main Methods:
- A cross-sectional, prospective study involving 1474 newborns in Rasht, Iran.
- G6PD activity was measured using both kinetic assay (quantitative) and fluorescent spot test (qualitative).
- Sensitivity, specificity, and predictive values of the FST were calculated.
Main Results:
- A prevalence of 6.6% for G6PD deficiency was observed among the studied newborns.
- Significant differences in mean G6PD levels were found between male and female newborns (P = 0.0001).
- A strong correlation was established between FST results and quantitative G6PD activity measurements (P < 0.0001).
Conclusions:
- The fluorescent spot test (FST) demonstrates acceptable sensitivity and specificity for G6PD deficiency screening in newborns.
- While FST is a useful screening tool, its diagnostic efficiency may be limited in certain situations.
- The study highlights the importance of accurate G6PD deficiency screening in neonates in the Rasht region.
Introduction:
Considering the high prevalence of glucose-6-phosphate dehydrogenase (G6PD) deficiency among newborns, different screening methods have been established in various countries. In this study, we aimed to assess the prevalence of G6PD deficiency among newborns in Rasht, Iran, and compare G6PD activity in cord blood samples, using quantitative and qualitative tests.
Methods:
This cross-sectional, prospective study was performed at five largest hospitals in Rasht, Guilan Province, Iran. The screening tests were performed for all the newborns, referred to these hospitals. Specimens were characterized in terms of G6PD activity under ultraviolet light, using the kinetic method and the qualitative fluorescent spot test (FST). We also determined the sensitivity, specificity, negative predictive value, and positive predictive value of the qualitative assay.
Results:
Blood samples were collected from 1474 newborns. Overall, 757 (51.4%) subjects were male. As the findings revealed, 1376 (93.4%) newborns showed normal G6PD activity, while 98 (6.6%) had G6PD deficiency. There was a significant difference in the mean G6PD level between males and females (P = 0.0001). Also, a significant relationship was detected between FST results and the mean values obtained in the quantitative test (P < 0.0001).
Conclusion:
According to the present study, FST showed acceptable sensitivity and specificity for G6PD activity, although it appeared inefficient for diagnostic purposes in some cases.
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