Understanding Your Laboratory Test: What It Is, Why It's Done, and What Your Results Mean
A urine test that measures acylcarnitine levels to help diagnose metabolic disorders affecting how the body breaks down fats.
{"Measures fatty acid metabolism byproducts in urine","Helps diagnose inherited metabolic disorders","Used for newborn screening follow-up and symptom evaluation","Involves collecting a simple urine sample","Results help doctors plan appropriate treatment"}
Key facts at a glance
- LOINC
- 9403-7
- Short code
- ACYU
- Synonyms
- Acylcarnitine Ur-mCnc
- Category
- chemistry
- Sample
- urine
- Container
- Sterile, clean-catch urine container (graded or plain)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- ≥ 0 years
- Method
- Tandem mass spectrometry (MS/MS)
- CPT
- 82017
- SNOMED
- 314862001
- Specimen volume
- 5-10 mL minimum; 10-20 mL preferred
- Stability
- Room temperature: 24 hours; Refrigerated (2-8°C): 5-7 days; Frozen (-20°C or below): 2-3 weeks. Protect from light.
- Hemolysis max
- 0
- Lipemia max
- 0
- Icterus max
- 0
- TAT
- 24–72 hours
- Order
- routine
This test is a laboratory analysis performed on a sample of your blood, urine, or other body fluid or tissue. It helps your healthcare provider evaluate how well your body is functioning and detect signs of disease, infection, or other health conditions that may require further evaluation or treatment.
The urine acylcarnitine test measures the levels of acylcarnitines in your urine. Acylcarnitines are compounds produced when fatty acids bind to carnitine, a substance that helps transport fatty acids into cells for energy production. This test helps doctors evaluate how well your body processes fats for energy.
Your doctor may order this test as part of a routine checkup, to help diagnose the cause of symptoms you are experiencing, to screen for a condition before it causes noticeable problems, or to monitor an ongoing illness and check how well your current treatment plan is working over time.
Doctors may order this test to: 1) Screen for or follow up on abnormal newborn screening results, 2) Investigate symptoms like unexplained fatigue, muscle weakness, or low blood sugar, 3) Diagnose fatty acid oxidation disorders and organic acidemias, and 4) Monitor patients already diagnosed with metabolic disorders.
The sample is usually collected at a laboratory, clinic, or hospital. A trained professional may draw a small amount of blood from a vein in your arm using a thin needle, or you may be asked to provide a urine sample or another specimen in a sterile container. Some tests require fasting beforehand, so always follow the specific instructions your healthcare provider gives you before your appointment.
A clean-catch urine sample is collected. You will be given instructions to clean the genital area before urinating, then collect a mid-stream urine sample in a sterile container. The sample should be taken to the lab promptly for processing.
Your results are compared with established reference ranges to determine whether your values fall within normal limits. Normal results generally suggest no evidence of the condition being tested for, while abnormal values may indicate an infection, deficiency, organ dysfunction, or other issue. Many factors, including medications, diet, and age, can influence results, so your provider will interpret them alongside your medical history and may recommend additional testing or follow-up.
Abnormal acylcarnitine levels in urine may indicate a problem with fatty acid metabolism. Your doctor will interpret results based on your specific pattern of acylcarnitines, clinical symptoms, and other test results. Further testing may be needed to confirm a diagnosis.
Reference range
Reference ranges vary by specific acylcarnitine species measured. Results are typically reported as micromoles per mole of creatinine (μmol/mol Cr) or as absolute concentrations (μmol/L). Each acylcarnitine (free carnitine C0, acetylcarnitine C2, propionylcarnitine C3, isovalerylcarnitine C5, octanoylcarnitine C8, etc.) has age-specific reference intervals. Consult laboratory-specific reference ranges.N/A
No fasting required. Collect random urine sample in clean, sterile container. Inform laboratory of patient age, clinical history, and any medications. Avoid contamination with fecal material.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
This test is crucial for detecting fatty acid oxidation disorders such as carnitine palmitoyltransferase (CPT) deficiency, medium-chain acyl-CoA dehydrogenase (MCAD) deficiency, and very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency. It also helps identify organic acidemias like propionic acidemia and methylmalonic acidemia. Early detection allows for dietary modifications, medication supplementation (like L-carnitine), and avoidance of fasting, which can prevent serious complications including metabolic crisis, organ damage, and developmental delays.
Frequently asked questions
Do I need to fast before this test?
Is this test only for children?
What happens if my results are abnormal?
How long does it take to get results?
Sources
- 1
- 2
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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