Association of Red Cell Glucose-6-Phosphate Dehydrogenase with Haemoglohinopathies

Publisher Website
Google Scholar
Abstract
A total of 1,112 randomly selected Saudi Arabs, of both sexes, living in Jeddah and the surrounding areas were screened for the phenotypic distribution of red cell glucose-6-phosphate dehydrogenase (G6PD) and 6-phosphogluconate dehydrogenase (6PGD). They were also investigated for haemoglobin and for thalassaemia. Phenotyping of the haemoglobins and the red cell enzymes was carried out by starch gel electrophoresis and the dye-decolouration screening test, while the investigation for thalassaemia was carried out by globin-chain biosynthesis, followed by column chromatography. The red cell Gd– alleles were significantly associated with the sickle-cell gene in both the males (χ21: AS-28.80; SS-4.89) and females (χ21: AS-10.99; SS-13.16). A similar association was also observed between G6PD deficiency and thalassaemias in males (χ21: α-thalassaemia – 3.13; β-thalassaemia – 11.06) and females (χ21: α-thalassaemia – 6.63). However, no such association was detected between red cell 6PGD types and haemoglobin genes. The results suggest that the red cell G6PD deficiency, sickle-cell and thalassaemia genes might have evolved as a result of the same ecological factor, probably malaria.