Test Code IA2 Islet Antigen 2 (IA-2) Antibody, Serum
Reporting Name
IA-2 Ab, SPerforming Laboratory
Mayo Clinic Laboratories in RochesterUseful For
Clinical distinction of type 1 from type 2 diabetes mellitus
Identification of individuals at risk of type 1 diabetes (including high-risk relatives of patients with diabetes)
Prediction of future need for insulin treatment in adult-onset diabetic patients
Method Name
Radioimmunoassay (RIA)
Ordering Guidance
-Distinguishing type 1 (autoimmune) diabetes mellitus from type 2 diabetes mellitus
-Identifying individuals at risk of type 1 diabetes (including high-risk relatives of patients with diabetes)
-Predicting future insulin requirement treatment in patients with adult-onset diabetes
Individual antibody testing would be more appropriate if 1, 2, or 3 of the analytes (GAD65, IA-2, insulin, ZnT8 antibodies) have already been tested and reported negative, and the provider wishes to test for the balance of remaining untested analytes only.
Specimen Required
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Collection Container/Tube:
Preferred: Red top
Acceptable: Serum gel
Submission Container/Tube: Plastic vial
Specimen Volume: 1.5 mL
Collection Instructions: Centrifuge and aliquot serum into a plastic vial.
Specimen Type
SerumSpecimen Minimum Volume
1 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Refrigerated (preferred) | 28 days | |
Frozen | 28 days | ||
Ambient | 72 hours |
Reject Due To
Gross hemolysis | Reject |
Gross lipemia | Reject |
Gross icterus | Reject |
Reference Values
≤0.02 nmol/L
Reference values apply to all ages.
Interpretation
Seropositivity for islet antigen 2 autoantibody (> 0.02 nmol/L) is supportive of:
-A diagnosis of type 1 diabetes
-A high risk for future development of diabetes
-A current or future need for insulin therapy in patients with diabetes
Day(s) Performed
Monday through Friday
Report Available
3 to 9 daysTest 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.CPT Code Information
86341
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
IA2 | IA-2 Ab, S | 81155-4 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
89588 | IA-2 Ab, S | 81155-4 |