G6PD Test
This test measures the amount of G6PD in your blood.
This test measures the amount of G6PD in your blood. G6PD stands for glucose-6-phosphate dehydrogenase. It's an enzyme, a protein that speeds up certain chemical reactions in your body. It helps your red blood cells work properly. Red blood cells move oxygen from your lungs to every cell in your body. Your cells need oxygen to grow, reproduce, and stay healthy. If you don't have enough G6PD, it's known as G6PD deficiency . This deficiency: It is a genetic disorder that is inherited (passed down from parent to child). It mainly affects men. Women can be affected, but they are more likely to be carriers of the defective gene. This means that they may not have symptoms, but they can still pass the gene on to their children. It is more common in people of African, Mediterranean, or Asian descent. G6PD deficiency can cause the destruction of your red blood cells. When red blood cells are destroyed faster than your body can replace them, it's called hemolytic anemia . If you have hemolytic anemia, your cells don't get all the oxygen they need. Most people with G6PD deficiency don't have symptoms until they are exposed to certain "triggers" which set off the destruction of red blood cells. Triggers can include: Fava beans, also called broad beans. Hemolytic anemia which happens after eating fava beans or inhaling pollen from fava plants is called favism. Viral infections . Bacterial infections . Certain antibiotics . Anti-malaria medicines. Other medicines, including nonsteroidal, anti-inflammatory drugs (NSAIDs) such as ibuprofen and aspirin. Other names: G6PD deficiency test, glucose-6-phosphate dehydrogenase test, G-6-PD, RBC G6PD test
Why is this test ordered? You may need a G6PD test if you have symptoms of hemolytic anemia. These include: Fatigue Pale skin or jaundice , a condition that causes your skin and eyes to turn yellow Rapid heart rate Shortness of breath Dark or yellow-orange colored urine (pee) Your newborn baby might need a G6PD test if they have jaundice that doesn't go away in two weeks and/or is not caused by another condition. Your baby may also be tested if you have a family history of G6PD deficiency.
Clinical Interpretation
If your results show you have lower than normal amounts of G6PD , it means you have a G6PD deficiency. But your symptoms and risk of getting hemolytic anemia can vary, depending on your personal health history and exposure to triggers. If you are a woman with slightly lower than normal amounts of G6PD , you may be a carrier of a G6PD deficiency. That means you have one defective G6PD gene and one normal G6PD gene. You might not have symptoms, since your normal G6PD genes usually make enough healthy red blood cells. But you have a risk of passing on the defective gene to your children. Male children are more likely to develop G6PD symptoms than female children. If you are a man with a normal amount of G6PD , you are unlikely to have a deficiency. If you have anemia, it may be due to another cause. Your provider may want to repeat the G6PD test in a few weeks if you had the test during an episode of hemolytic anemia. Learn more about laboratory tests, references ranges, and understanding results .
Clinical Protocol & Patient Advice
- 1
There are no special preparations needed for a G6PD test.
Usage Guidance
- Reference ranges vary by laboratory. Always discuss your specific results with a qualified healthcare professional.
Source: MedlinePlus, National Library of Medicine. View the original.