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Test ID PCAB Parietal Cell Antibodies, IgG, Serum

Useful For

Evaluating patients suspected of having pernicious anemia or immune-mediated deficiency of vitamin B12 with or without megaloblastic anemia

Method Name

Enzyme-Linked Immunosorbent Assay (ELISA)

Reporting Name

Parietal Cell Ab, IgG, S

Specimen Type

Serum

Container/Tube:

Preferred: Serum gel

Acceptable: Red top

Specimen Volume: 0.5 mL

Forms: If not ordering electronically, complete, print, and send a Neurology Test Request Form-General (T732) with the specimen (http://www.mayomedicallaboratories.com/it-mmfiles/neurology-request-form.pdf)

Specimen Minimum Volume

0.45 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Refrigerated (preferred) 21 days
  Frozen  21 days

Clinical Information

Pernicious anemia (PA) is characterized by atrophic body gastritis (ABG) and is the end state of a progressive disease known as autoimmune chronic atrophic gastritis.(1) In this disease, immune-mediated inflammation leads to destruction of gastric parietal cells with the resultant loss of intrinsic factor production and the inability to absorb dietary vitamin B12. Diagnosis of PA involves demonstrating the presence of a macrocytic anemia in the context of vitamin B12 deficiency, as well as documenting positive autoantibody serology, specifically anti-parietal cell antibody (PCA) and intrinsic factor antibody (IFA).(2) PCAs bind to the alpha- and beta-subunits of the membrane-bound H(+)/K(+)-ATPase. In contrast, IFAs bind directly to intrinsic factor, blocking its ability to bind vitamin B12.(1,2) Both PCAs and IFAs are useful diagnostic markers for PA. In a recently published study, PCAs were 81% sensitive and 90% specific for ABG, while IFAs were 27% sensitive and 100% specific. The study concluded that a combination of PCA and IFA testing was the optimal strategy for the evaluation of patients with suspected PA.(4)

Reference Values

Negative: ≤20.0 Units

Equivocal: 20.1-24.9 Units

Positive: ≥25.0 Units 

Reference values apply to all ages.

Cautions

The presence of immune complexes or other immunoglobulin aggregates in the patient specimen may cause an increased non-specific binding and produce false-positive results in this assay.

 

A negative result does not rule out the presence of parietal cell antibodies; the concentration of antibody may be below the detection limit of the assay.

 

A positive result only indicates the presence of antibody to H(+)/K(+) ATPase and does not necessarily indicate the presence of autoimmune disease or other diseases.

 

The assay performance has not been established for pediatric patients.

 

Results of this assay should be used in conjunction with clinical findings and other serological tests.

 

The assay performance characteristics have not been established for matrices other than serum.

Day(s) Performed

Monday, Wednesday, Friday; 3 p.m.

Report Available

1 day

Performing Laboratory

Mayo Medical Laboratories in Rochester

Test Classification

This test has been cleared or approved by the U.S. Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.

CPT Code Information

83516

NY State Approved

Yes