Gliadin Antibodies (IgA and IgG)

Message
Sendout, Mayo test code: DGLDN


Test Code
LAB725


Alias/See Also
Celiac Disease
Coeliac Disease
Gliadin Antibodies IgG and IgA
DGLDN


CPT Codes
86258x2

Preferred Specimen
0.5 mL serum from a gold serum gel tube


Minimum Volume
0.4 mL


Other Acceptable Specimens
Red tube


Instructions
Centrifuge and aliquot serum into a plastic vial.


Transport Container
Plastic vial


Transport Temperature
Refrigerated


Specimen Stability
Refrigerated (preferred): 21 days
Frozen: 21 days


Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Hemolysis: Mild OK; Gross reject
Lipemia: Mild OK; Gross reject
Icterus: Mild OK; Gross OK


Methodology
Enzyme-Linked Immunosorbent Assay (ELISA)

FDA Status
Approved

Setup Schedule
Monday, Wednesday, Friday


Report Available
2-4 days


Limitations
This test should not be solely relied upon to establish a diagnosis of celiac disease. It should be used to identify patients who have an increased probability of having celiac disease and in whom a small intestinal biopsy is recommended.
 
Affected individuals who have been on a gluten-free diet prior to testing may have a negative result.
 
For individuals who test negative, IgA deficiency should be considered. If total IgA is normal and deamidated gliadin IgA is negative, there is a low probability of the patient having celiac disease and a biopsy may not be necessary.
 
If serology is negative or there is substantial clinical doubt remaining, then further investigation should be performed with endoscopy and bowel biopsy. This is especially important in patients with frank malabsorptive symptoms since many syndromes can mimic celiac disease. For the patient with frank malabsorptive symptoms, a bowel biopsy should be performed regardless of serologic test results.
 
Testing for IgA and IgG antibodies to unmodified gliadin proteins is no longer recommended because of the low sensitivity and specificity of these tests for celiac disease.
 
This test should not be ordered as a replacement for TSTGP / Tissue Transglutaminase Antibodies, IgA and IgG Profile, Serum.


Reference Range
Included with report


Clinical Significance
Assessment of deaminated gliadin IgA and IgG antibodies for evaluating patients suspected of having celiac disease, including patients with compatible clinical symptoms, patients with atypical symptoms, and individuals at increased risk (family history, previous diagnosis with associated disorder, positivity for HLA DQ2 and/or DQ8).
 
Monitoring response to a gluten-free diet in patients with celiac disease.


Performing Laboratory
Mayo Clinic Laboratories, Rochester, Minnesota

Additional Information
Gliadin (Deamidated) Antibodies Evaluation, IgG and IgA, Serum


The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.