Glucose-6-phosphate dehydrogenase deficiency is the most common enzyme disorder in humans. The life-long genetic disorderis highly common in malaria-endemic areas, yet it can makemalaria treatment deadly. Should testing for a disorder so prevalent be a standard of antenatal care?
In 1989, the World Health Organization stated that Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzyme disorder in humans, affecting approximately 400 million people around the globe. As G6PD deficiency is an X-linked disorder, the disorder affects mostly males. However, G6PD deficiency also affects a large number of females due to the high prevalence of the gene in malaria-endemic areas. G6PD deficiency is most common in malaria-endemic areas, which in some areas can affect over 20% of the population. These areas include Sub-Saharan Africa, the Middle East, the Mediterranean, and parts of southern Asia. Glucose-6-phosphate dehydrogenase deficiency can cause hemolytic anemia and is often responsible for neonatal jaundice, a condition that can cause brain damage, death, and or other disorders and complications.
Glucose-6-phosphate dehydrogenase deficiency is an X-linked disorder that results in abnormally low levels of Glucose-6-phosphate dehydrogenase, an enzyme that is important to glycolysis and the protection of red blood cells from oxidative damage. Glycolysis is the breakdown of glucose (C6H12O6), an important source of energy in humans, into usable energy for the body. In the absence of Glucose-6-phosphate dehydrogenase, more red blood cells may be destroyed than are produced, causing hemolytic anemia.
When hemolytic anemia is left untreated, a person may develop heart arrhythmias, cardiomyopathy, and heart failure. Acute hemolytic crises can occur in people with G6PD deficiency due to interactions with certain drugs and fava beans, infections, diabetic ketoacidosis, and spontaneously in neonates and may lead to acute renal failure and or death.
Glucose-6-phosphate dehydrogenase deficiency may also cause neonatal jaundice. Neonatal jaundice, or neonatal hyperbilirubinemia, is a condition caused by excess bilirubin in the body. Bilirubin is a pigment that is released when red blood cells are destroyed, which can be harmful to the body in excess. Hence, the destruction of red blood cells and hemolytic anemia due to G6PD deficiency may cause neonatal jaundice. When left untreated, neonatal jaundice can cause hemorrhage, sepsis, infection, liver malfunction, spastic cerebral palsy, kernicterus, and biliary atresia (Mayo Clinic, 2020), disorders that can lead to brain damage, organ damage, and death. Neonatal jaundice can be easily and inexpensively treated with phototherapy.
In pregnancy, women with G6PD deficiency experience a higher rate of spontaneous abortions and low erythrocyte counts during puerperal period than in women that are not G6PD deficient. Infants born to G6PD deficient mothers often have lower birth weights than those of non-G6PD deficient mothers.
While many people that carry the gene for G6PD deficiency are asymptomatic, G6PD deficiency is a serious health concern for many, especially in malaria-endemic areas. Infection with malaria is complicated by G6PD deficiency, as people affected by the deficiency may have a life-threatening hemolytic crisis in reaction to drugs used in malaria treatment. People with G6PD deficiency may also experience hemolytic crises in reaction to other drugs such as sulphonamides, sulphones, and antibacterial compounds and fava beans.
Many studies suggest that males with G6PD deficiency have higher immunity againstPlasmodium falciparum malaria than those without G6PD deficiency, which lends itself to the high prevalence of genetic G6PD deficiency in areas where malaria is common or was previously common.
Glucose-6-phosphate dehydrogenase deficiency is a major public health concern globally. Accessibility to information and testing for Glucose-6-phosphate dehydrogenase deficiency is crucial to the health and livelihood of people all over the world, but especially in malaria-endemic areas. G6PD deficiency screening of neonates and education of parents and guardians of G6PD deficiency and the dangers of neonatal jaundice has been found effective to prevent hemolytic crises from drug and fava bean interactions and kernicterus from untreated hyperbilirubinemia. Guardians of a child with G6PD deficient infants must be mindful of the drugs and food the child consumes and parents that breastfeed infants with G6PD deficiency should avoid ingestion of fava beans or drugs that could harm the child. Likewise, it is important for individuals to know if they are G6PD deficient.
By Julia Doo, longtime collaborator and researcher with Maternova and with Meg Wirth, Founder
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Unique Identifier: UN7758687 Headline: UN Mission Gives Medical Treatment in Liberia Caption Description: Medical staff of the Chinese Contingent of the United Nations Mission in Liberia (UNMIL) perform an ultra-sound in their clinic, open to all national citizens in their area of operation in Zwedru, Liberia. Country: Liberia Production Date: 4/23/2005 7:49:05 PM
Identification of anemia in pregnant women is important, since it is an important cause of multiple complications during pregnancy (preterm delivery, low birth weight and perinatal death), so it is recommended to all pregnant women, in the first prenatal visit and at 28 weeks of gestation, the measurement of serum concentrations of hemoglobin and hematocrit as a screening test for anemia.
Prenatal assessment seeks to identify, through clinical history, sociodemographic characteristics, mean blood pressure, Doppler of the uterine arteries and biochemical markers such as pregnancy-associated plasma protein A (PAPP-A) and placental growth factor (PlGF), those women who are at high risk of developing preeclampsia in order to take appropriate measures. that can help reduce that risk.