Test Code LAB0285155 Intrinsic Factor Blocking Antibody, Serum
Additional Codes
Mayo Test ID |
---|
IFBA |
Performing Laboratory
Mayo Clinic Laboratories in RochesterUseful For
Confirming the diagnosis of pernicious anemia
Testing Algorithm
For more information, see Vitamin B12 Deficiency Evaluation.
Special Instructions
Method Name
Immunoenzymatic Assay
Reporting Name
Intrinsic Factor Blocking Ab, SSpecimen Type
SerumOrdering Guidance
For a comprehensive workup of patients with suspected pernicious anemia, order ACASM / Pernicious Anemia Cascade, Serum, which initiates testing with measurement of vitamin B12. Depending of the vitamin B12 concentration, testing for intrinsic factor blocking antibody, gastrin, and methylmalonic acid may be added.
Specimen Required
Patient Preparation:
1. Patient should be fasting for 8 hours.
2. This test should not be performed on patients who have received a vitamin B12 injection or radiolabeled vitamin B12 injection within the previous 2 weeks.
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions: Centrifuge and aliquot serum into a plastic vial.
Specimen Minimum Volume
0.5 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Refrigerated (preferred) | 14 days | |
Frozen | 14 days |
Reject Due To
Gross hemolysis | Reject |
Gross lipemia | OK |
Reference Values
Negative
Interpretation
The aim of the work-up of patients with suspected vitamin B12 deficiency is to first confirm the presence of deficiency and then to establish its most likely etiology.
Measurement of serum vitamin B12, either preceded or followed by serum methylmalonic acid measurement, is the first step in diagnosing pernicious anemia (PA). If these tests support deficiency, then intrinsic factor blocking antibody (IFBA) testing is indicated to confirm PA as the etiology. A positive IFBA test very strongly supports a diagnosis of PA. Since the diagnostic sensitivity of IFBA testing for PA is only around 50%, an indeterminate or negative IFBA test does not exclude the diagnosis of PA. In these patients, either PA or another etiology, such as malnutrition, may be present. Measurement of serum gastrin levels will help in these cases. In patients with PA, fasting serum gastrin is elevated to more than 200 pg/mL in an attempted compensatory response to the achlorhydria seen in this condition.
For a detailed overview of the optimal testing strategies in PA diagnosis, see ACASM / Pernicious Anemia Cascade, Serum and associated Vitamin B12 Deficiency Evaluation.
Day(s) Performed
Monday through Friday
Report Available
1 day to 3 daysSpecimen Retention Time
2 weeksTest Classification
This test has been cleared, approved, or is exempt by the US 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
86340
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
IFBA | Intrinsic Factor Blocking Ab, S | 31444-3 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
IFBLA | Intrinsic Factor Blocking Ab, S | 31444-3 |
CMT31 | Comment | 48767-8 |