Blood Test Overview: What It Is, Why It Is Done, and What Your Results Mean
This test measures the level of 3-Hydroxyoleoylcarnitine in amniotic fluid to evaluate fetal fatty acid metabolism.
{"A specialized test performed during pregnancy to assess fetal metabolic health","Helps detect potential fatty acid oxidation disorders before birth","Involves analyzing a sample of amniotic fluid collected during amniocentesis","Abnormal results may indicate metabolic conditions requiring early intervention","Part of expanded newborn screening and prenatal metabolic assessment"}
Key facts at a glance
- LOINC
- 50115-5
- Short code
- 3OH-Oleoylcarn Amn-sCnc
- Synonyms
- 3OH-Oleoylcarn Amn-sCnc
- Category
- chemistry
- Sample
- fluid
- Container
- Sterile tube
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Specimen volume
- 2-5 mL
- Stability
- Room temperature: 2h, Refrigerated: 24h
- Hemolysis max
- 300
- TAT
- 4–24 hours
- Order
- routine
This test is a laboratory analysis that measures specific substances in a sample of your blood or other body fluid to help your doctor evaluate how well your body is functioning and to look for signs of illness.
The 3-Hydroxyoleoylcarnitine (C18:1-OH) test measures the concentration of a specific fatty acid metabolite in amniotic fluid. This substance is a byproduct of fatty acid metabolism and normally appears at very low levels. The test uses a sample of amniotic fluid collected during amniocentesis to detect whether abnormal accumulations are present, which could signal metabolic disorders in the developing fetus.
Your doctor may order this test to screen for disease before symptoms appear, to help diagnose the cause of symptoms you are experiencing, to monitor an ongoing condition, or to check how well a treatment is working.
This test is primarily used for prenatal screening of fatty acid oxidation disorders. These are inherited metabolic conditions where the body cannot properly break down fatty acids for energy. Detecting elevated 3-Hydroxyoleoylcarnitine levels during pregnancy allows healthcare providers to prepare for appropriate management and treatment immediately after birth, which can significantly improve outcomes for affected infants.
A trained healthcare professional will collect the sample, usually by drawing a small amount of blood from a vein in your arm with a thin needle, or by asking you to provide a urine sample. The procedure is quick, and most people return to normal activities right away.
The test requires a sample of amniotic fluid, which is collected through a procedure called amniocentesis. During amniocentesis, a thin needle is inserted through the abdomen into the uterus to withdraw a small amount of amniotic fluid. The sample is then sent to a laboratory where specialized equipment measures the levels of 3-Hydroxyoleoylcarnitine using mass spectrometry techniques.
Your results are compared with standard reference ranges. Values within these ranges are generally considered normal, while higher or lower values may suggest infection, inflammation, an organ problem, or another condition that needs further evaluation. Your doctor will explain what your specific numbers mean for your health.
Results are reported as moles per volume. Normal levels of 3-Hydroxyoleoylcarnitine in amniotic fluid are typically very low or undetectable. Elevated levels may indicate that the fetus has a fatty acid oxidation disorder, such as medium-chain acyl-CoA dehydrogenase deficiency (MCAD) or other similar conditions. Your healthcare provider will interpret the results in context with other clinical findings and may recommend additional testing or genetic counseling.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
Elevated 3-Hydroxyoleoylcarnitine in amniotic fluid is a key indicator of fetal fatty acid oxidation disorders. These inherited metabolic conditions can cause serious health problems, including hypoketotic hypoglycemia, liver dysfunction, and cardiac complications. Early detection through prenatal testing enables healthcare teams to plan for immediate specialized care after delivery, including dietary management and avoidance of fasting, which can prevent life-threatening complications. The test is particularly valuable for families with a history of metabolic disorders or when routine prenatal screening suggests possible abnormalities.
Frequently asked questions
Is this test part of routine prenatal care?
Does an abnormal result mean my baby will definitely have a health problem?
What are the risks of having this test?
If the test is abnormal, what happens next?
Sources
- 1
- 2
- 3
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy