Related Experiment Video
Updated: Jul 7, 2026

Spectrophotometric Methods for the Study of Eukaryotic Glycogen Metabolism
Published on: August 19, 2021
Prevalence of glucose-6-phosphate dehydrogenase deficiency in Northern Greece
G Ntaios1, A Chatzinikolaou, C Tomos
1First Propedeutic Department of Internal Medicine, AHEPA Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece. ntaiosgeorge@yahoo.gr
Insights
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is prevalent in Northern Greece, affecting 6.3% of the screened population. This study highlights a higher prevalence in males and suggests a significant public health concern in the region.
Area of Science:
- Medical Genetics
- Biochemistry
Background:
- Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a global health issue affecting over 400 million people.
- Prevalence varies significantly across geographic and demographic groups.
Purpose of the Study:
- To determine the prevalence of G6PD deficiency in Northern Greece.
- To compare regional prevalence with the general Greek population.
Main Methods:
- Screened 5161 newborns and adults between July 2001 and March 2007.
- Utilized the dye reduction method for G6PD deficiency detection.
Main Results:
- Identified a 6.3% overall prevalence of G6PD deficiency.
- Moderate deficiency found in 2.7% and complete deficiency in 3.7% of subjects.
- Prevalence in males was nearly double that in females.
Conclusions:
- Northern Greece exhibits a higher prevalence of G6PD deficiency than the general Greek population.
- The higher prevalence in males warrants further investigation and targeted health strategies.
Abstract:
Glucose-6-phosphate dehydrogenase (G6PD) deficiency affects more than 400 million persons worldwide. Its distribution varies significantly among different geographic regions and different population groups. Purpose of our study was to estimate its prevalence in Northern Greece. The dataset comprised 5161 newborns and adults who were screened for G6PD deficiency between July 2001 and March 2007. G6PD deficiency was detected by the dye reduction method. In the screened group, 6.3% of subjects were G6PD deficient. Moderate enzyme deficiency was shown in 139 individuals (2.7%). Complete deficiency was identified in 3.7%. The prevalence of G6PD deficiency in Northern Greece is much higher compared with the general Greek population. Moreover, G6PD prevalence in the male sex is much higher - almost double - that in the female sex.
Related Concept Videos
Inborn Errors of Metabolism
Glucose Transporters
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
Hyperglycemia
Type II Diabetes Mellitus III: Clinical Manifestations and Diagnosis
Hypoglycemia and Glucagon
Diabetes: Symptoms, Diagnosis, and Complications

