Histamine Release (Chronic Urticaria)
Additional Codes
LAB7133
Alternative Name(s)
Anti-IgE Receptor,Chronic Urticaria,FCER1, Chronic Urticaria,FC Epsilon Receptor Antibody,CU (Chronic Urticaria)
Performing Laboratory
Quest Diagnostics Nichols Institute - San Juan Capistrano, CA
Methodology
Cell Culture (CC) • Immunoassay (IA)
Assay Category
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes
Specimen Requirements
Preferred Specimen(s)
1.5 mL serum collected in a red-top tube (no gel)
Minimum Volume
1 mL
Transport Container
Transport tube
Transport Temperature
Room temperature
Specimen Stability
- Room temperature: 7 days
- Refrigerated: 7 days
- Frozen: 30 days
Reject Criteria
Gross hemolysis • Grossly lipemic • Icteric • Specimen other than serum • Serum Separator Tube (SST®)
Day(s) Test Set Up
Tues, Thurs a.m.; Results available 3-7 days
Test Classification and CPT Coding
86343
Clinical Significance
Histamine Release (Chronic Urticaria) - Chronic Urticaria (CU) is a common skin disorder affecting 1 to 6% of the general population. It is characterized by repeated occurrence of short-lived cutaneous wheals accompanied by redness and itching. Autoimmune urticaria is defined by the presence of a functional IgG antibody to high-affinity IgE receptor (Fc epsilon RI alpha) or IgE. These antibodies trigger mast cell and basophil degranulation by the engagement of Fc epsilon receptor. Functional IgG antibody to the receptor has been identified in approximately 30-40% of patients with CU, and anti IgE antibody has been identified in another 5%-10%.
Patient Preparation
Patients taking calcineurin inhibitors should stop their medication for 72 hours prior to draw
Reference Range
<16 %