Platform
Company
Immunology & Autoimmune
Review status
Currently under review
Pending specialist review and validation.
The C8/C10 MCAD test measures the ratio of two medium-chain acylcarnitines in your blood, octanoylcarnitine (C8) and decanoylcarnitine (C10). These molecules reflect how your cells break down certain fats for energy through the fatty acid oxidation pathway.
It is typically performed as part of a comprehensive acylcarnitine profile by tandem mass spectrometry, using a small blood sample from a vein or a dried blood spot. Clinicians use this ratio to help evaluate for medium-chain acyl-CoA dehydrogenase deficiency, a genetic condition that affects energy production, especially during fasting or illness.
An abnormal C8/C10 ratio can suggest a problem with the enzyme that processes medium-chain fats, which may lead to low blood sugar, lethargy, seizures, or liver stress during periods without food or during infections. Identifying this pattern early allows steps to prevent metabolic crises and to guide safe nutrition and sick-day plans.
Your clinician may order this test as follow-up to newborn screening, to investigate symptoms like vomiting after fasting, poor tolerance to illness, or unexplained episodes of low energy, or when there is a family history. It can also support monitoring in people with a known diagnosis.
Your result is interpreted together with your symptoms, exam findings, and other laboratory tests, such as the absolute C8 level, a full acylcarnitine profile, and urine organic acids. Genetic testing of the ACADM gene may be recommended if the pattern suggests medium-chain acyl-CoA dehydrogenase deficiency.
If your ratio is outside the expected range, your healthcare professional may repeat testing when you are well, check carnitine status, and refer you to a metabolic specialist. Most people who are identified and follow dietary and illness management plans do well. Do not change feeding or fasting practices without medical guidance.
Reference intervals vary by laboratory, analyzer, methodology, population, and units. The ranges shown here are for education only. Always interpret your results against the reference interval printed on your own lab report.
Infections, vomiting, fever, or prolonged time without eating can shift acylcarnitine patterns and may accentuate abnormalities. Tell your clinician if you were sick or fasting around the time of the test.
Results can differ between plasma and dried blood spot testing, and with timing relative to meals. Consistent collection conditions help your care team compare results over time.
Certain drugs and products can alter acylcarnitines, including valproate, pivalate-containing antibiotics, and medium-chain triglyceride oils. Share all prescriptions and supplements you take.
Low carnitine levels can change the acylcarnitine profile and complicate interpretation. Your clinician may check free and total carnitine alongside this test.
Newborns, premature infants, and babies early in life can have different patterns due to feeding adaptation and maternal influences. Follow-up testing is often tailored to age.
Physiologic changes in pregnancy and breastfeeding can affect metabolism and acylcarnitine levels. Your provider may interpret results with these factors in mind.
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