6-Phosphogluconate dehydrogenase deficiency can be asymptomatic in many patients who are carriers. Female carriers have been found to be at a higher frequency experiencing symptoms. Enzyme activity was shown to be reduced by 35–65% depending on the severity of the deficiency. Abnormal red blood cell breakdown in 6PGD deficiency can be symptomatic in a number of ways, including the following:
6PGD deficiency is a recessive hereditary disorder located on the P arm of chromosome 1. It is an autosomal disease, not associated with the sex chromosomes and can affect both sexes. The lack of synthesis of a specific protein on chromosome 1 has reduced a subject suffering from 6PGD deficiency from producing adequate amounts of the 6-Phosphogluconate dehydrogenase enzyme. Transfer of the disease can be passed from a parent, even when the parent is asymptomatic.
People suffering from 6PGD and/or G6PD deficiencies are therefore at risk of hemolytic anemia in states of oxidative stress. Oxidative stress can result from infection and from chemical exposure to medication and certain foods. Broad beans, e.g., fava beans, contain high levels of vicine, divicine, convicine and isouramil, all of which are oxidants. When all remaining reduced glutathione is consumed, enzymes and other proteins, such as hemoglobin are subsequently damaged by the free radicals, leading to electrolyte imbalance, cross-bonding and protein deposition in the redcell membranes. Damaged red cells are phagocytosed and sequestered in the spleen. The hemoglobin is metabolized to bilirubin. The red blood cells rarely disintegrate in the circulation, so hemoglobin is rarely excreted directly by the kidney, but this can occur in severe cases, causing acute kidney injury.
Diagnosis
Treatment
Prevention
The most important measure taken for treatment of 6-phosphoglucanate dehydrogenase is prevention. Avoidance of chemical exposures to drugs and foods that have the potential to cause hemolysis. Although some foods and supplements have antioxidant properties, their use does not decrease the severity of G6PD deficiency. Diagnosis is difficult during haemolytic episodes since reticulocytes have increased levels of enzymes and may get erroneously normal result. wait until steady state may prevent infection-induced attacks.
In the acute phase of hemolysis, blood transfusions might be necessary, or even dialysis in acute kidney injury. Blood transfusion is an important symptomatic measure, as the transfused red cells are generally not 6PGD deficient and will live a normal lifespan in the recipient's circulation.