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Understanding Your Diagnostic Lab Test: What It Is, Why It Matters, and What to Expect

Published: August 9, 2026Updated: August 16, 2026

This blood test measures the ratio of acylcarnitine to free carnitine (C0) to help detect certain metabolic disorders.

Quick summary

{"The test measures carnitine levels in the blood to check metabolic function","It helps screen for inherited metabolic disorders affecting fatty acid oxidation","A small blood sample is collected, usually from a finger prick or heel stick","Abnormal results may indicate problems with how the body converts fat into energy","Follow-up testing is often needed if results are abnormal"}

Medically reviewed by WellAlly Editorial TeamLast reviewed August 16, 2026Editorial policy

Key facts at a glance

LOINC
59249-3
Short code
AC/C0 Ratio
Synonyms
Acylcarnitine/Acyl+C0 DBS-sRto
Category
chemistry
Sample
serum
Container
Dried Blood Spot (DBS) filter paper collection card
Units
N/A
Ref low
0.02
Ref high
0.25
Critical range
— – 0.5 N/A
Fasting
false
Population
adult
Sex
all
Age range
≥ 0 years
Method
Tandem Mass Spectrometry (MS/MS)
CPT
82017
SNOMED
122269009
Specimen volume
3-4 complete spots (approximately 100-120 μL blood total)
Stability
Room temperature: 7 days; Refrigerated (2-8°C): 14 days; Frozen (-20°C): 30+ days
Hemolysis max
500
Lipemia max
1000
Icterus max
500
TAT
24–72 hours
Order
routine

This test is a laboratory procedure that helps your doctor evaluate your health by measuring specific substances or markers in a sample from your body, such as blood or urine, in order to detect a medical condition, monitor an existing diagnosis, or screen for problems before symptoms appear.

The acylcarnitine to free carnitine (C0) ratio test is a blood test that measures the balance between two forms of carnitine in your blood. Carnitine is a substance that helps your body turn fat into energy. This test is often used as part of newborn screening programs to detect certain metabolic disorders that affect how the body processes fatty acids.

This test is important because it can reveal early signs of disease, confirm or rule out a diagnosis, guide your doctor's treatment decisions, and help track how well a therapy is working over time, allowing health problems to be addressed promptly and reducing the risk of complications.

Carnitine plays a crucial role in energy production. Free carnitine (C0) helps transport fatty acids into cells where they are burned for energy. Acylcarnitines are created when carnitine binds to fatty acids. The ratio between these two forms helps doctors understand if the body's energy production system is working properly. An abnormal ratio may suggest metabolic disorders such as carnitine transport defects or fatty acid oxidation disorders.

The test is usually performed by a trained healthcare professional who collects a small sample, such as blood drawn from a vein in your arm or a urine specimen, which is then sent to a laboratory for analysis; the procedure is typically quick, requires no special preparation unless your doctor advises otherwise, and causes only minimal, temporary discomfort.

A healthcare professional will collect a small blood sample, typically from a finger prick or heel (in newborns). The blood is then analyzed in a laboratory to measure the levels of acylcarnitine and free carnitine, and calculate their ratio. The test is often part of a larger newborn screening panel.

Reference range

Acylcarnitine/Carnitine Free (C0) ratio: 0.02-0.25 (varies by laboratory methodology and reference population)N/A

Specimen: serum

No fasting required. Test is typically collected as part of routine newborn screening 24-72 hours after birth. For non-newborn patients, no special preparation required.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

This test is primarily used to screen for inherited metabolic disorders, particularly those affecting fatty acid oxidation. Normal ratios indicate proper carnitine metabolism and energy production from fats. Abnormal ratios may suggest conditions such as primary carnitine deficiency, multiple acyl-CoA dehydrogenase deficiency, or other fatty acid oxidation disorders. These conditions can lead to serious health problems if not detected and treated early, including muscle weakness, heart problems, and metabolic crises. Treatment often involves dietary modifications and carnitine supplementation.

Frequently asked questions

Do I need to fast before this test?
Your doctor will provide specific instructions. For newborn screening, fasting is not typically required. For older children or adults, fasting may be recommended as it can affect fatty acid levels in the blood.
Is this test painful?
The test involves a brief finger prick or heel stick, which may cause minor discomfort similar to a small pinch. The pain is usually very short-lived.
What do abnormal results mean?
Abnormal results do not always mean your baby has a serious condition. Sometimes abnormal results can be due to prematurity or other factors. If results are abnormal, your doctor will typically order additional tests to confirm or rule out specific conditions.
How long does it take to get results?
Results are usually available within a few days to a week, depending on the laboratory. Newborn screening results are often available within 1-2 weeks after collection.
Is treatment available if a disorder is detected?
Yes, many metabolic disorders detected through this test can be managed effectively with early treatment. This may include special diets, medications, and regular monitoring. Early detection and treatment can prevent serious complications and improve long-term outcomes.
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

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