Alpha-Fetoprotein (AFP) Test
The alpha-fetoprotein (AFP) test is a blood test performed during pregnancy to assess the risk of certain birth defects and genetic conditions in a developing baby.
Overview
An AFP test measures the level of alpha-fetoprotein in your blood. AFP is a protein primarily produced in the liver of a developing fetus. While some AFP naturally passes into the mother's blood, abnormal levels—either higher or lower than expected—may indicate an increased risk for specific health conditions. This test is typically conducted between 15 and 20 weeks of pregnancy.
For individuals who are not pregnant, this test may be used as an AFP tumor marker test to help diagnose certain cancers, particularly liver cancer.
Conditions Associated with Abnormal AFP Levels
Abnormal levels may suggest an increased risk for the following:
- Neural tube defects: Serious conditions where the baby's brain, spine, or spinal cord do not form properly, such as spina bifida or anencephaly.
- Down syndrome: A genetic disorder affecting physical and mental development.
- Edwards syndrome (trisomy 18): An uncommon genetic condition often involving organ defects and abnormal head shape.
- Abdominal or esophageal defects: Issues involving the baby's belly or the tube connecting the mouth to the stomach.
Why the Test is Performed
The test is routinely offered during the second trimester. Providers may specifically recommend it if you are at a higher risk due to:
- A family history of birth defects.
- Maternal age of 35 years or older.
- A diagnosis of diabetes.
- Use of certain medications or drugs during pregnancy that could harm the baby.
The AFP test is often part of a broader prenatal screening, such as a multiple marker test (triple screen) or a quad screen.
Understanding Results
It is important to note that this test cannot diagnose a condition; it only indicates risk levels. Results can be influenced by factors such as an incorrect due date, carrying multiple babies, or a false positive result.
- Lower than normal levels: May indicate an increased risk for genetic disorders like Down syndrome or Edwards syndrome.
- Higher than normal levels: May indicate an increased risk for neural tube defects or abdominal/esophageal defects.
If results are abnormal, your healthcare provider will typically order follow-up testing to investigate further.