Test ID CARN Carnitine, Plasma
Useful For
Evaluation of patients with a clinical suspicion of a wide range of conditions including organic acidemias, fatty acid oxidation disorders, and primary carnitine deficiency using plasma specimens
Highlights
Carnitine levels are disturbed in primary disorders of the carnitine cycle, or secondary disturbances of carnitine metabolism due to other biochemical disorders.
Additional testing is required to distinguish between primary and secondary deficiencies of carnitine.
Dietary intake (meat, carnitine supplementation) may cause increased carnitine values.
Abnormal results are accompanied by detailed interpretation including recommendations for follow-up testing.
Method Name
Flow Injection Analysis-Tandem Mass Spectrometry (FIA-MS/MS)
Reporting Name
Carnitine, PSpecimen Type
PlasmaNecessary Information
Patient's age is required.
Specimen Required
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Collection Container/Tube:
Preferred: Green top (sodium heparin)
Acceptable: Lavender top (EDTA), green top (lithium heparin)
Submission Container/Tube: Plastic vial
Specimen Volume: 0.5 mL
Collection Instructions: Centrifuge and aliquot plasma into a plastic vial
Specimen Minimum Volume
0.2 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Plasma | Frozen (preferred) | 60 days | |
Refrigerated | 21 days | ||
Ambient | 7 days |
Reference Values
|
Total carnitine (TC) |
Free carnitine (FC) |
Acylcarnitine (AC) |
AC/FC Ratio |
Age Group |
Range* |
Range* |
Range* |
Range |
≤1 day |
23-68 |
12-36 |
7-37 |
0.4-1.7 |
2-7 days |
17-41 |
10-21 |
3-24 |
0.2-1.4 |
8-31 days |
19-59 |
12-46 |
4-15 |
0.1-0.7 |
32 days-12 months |
38-68 |
27-49 |
7-19 |
0.2-0.5 |
13 months-6 years |
35-84 |
24-63 |
4-28 |
0.1-0.8 |
7-10 years |
28-83 |
22-66 |
3-32 |
0.1-0.9 |
11-17 years |
34-77 |
22-65 |
4-29 |
0.1-0.9 |
≥18 years |
34-78 |
25-54 |
5-30 |
0.1-0.8 |
*Values expressed as nmol/mL
Schmidt-Sommerfeld E, Werner E, Penn D: Carnitine plasma concentrations in 353 metabolically healthy children. Eur J Pediatr. 1988;147:356-360
Used with permission of European Journal of Pediatrics.
Day(s) Performed
Monday through Friday
Performing Laboratory
Mayo Clinic Laboratories in RochesterCPT Code Information
82379
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
CARN | Carnitine, P | 97182-0 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
32050 | Total | 14288-5 |
32051 | Free (FC) | 14286-9 |
32052 | Acylcarnitine (AC) | 14282-8 |
21032 | AC/FC Ratio | 30193-7 |
21549 | Interpretation | 59462-2 |
Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.Report Available
3 to 5 daysNY State Approved
YesForms
If not ordering electronically, complete, print, and send a Biochemical Genetics Test Request (T798) with the specimen.