Test Code 1433E 14-3-3 eta, Serum
Specimen Required
Supplies: Sarstedt Aliquot Tube 5 mL (T914)
Collection Container/Tube: Serum gel
Submission Container/Tube: Plastic vial
Specimen Volume: 0.5 mL Serum
Collection Instructions: Centrifuge and aliquot serum into a plastic vial.
Useful For
A potentially improved approach for the early identification of patients at-risk for or with early and established rheumatoid arthritis (RA) in combination with specific autoantibody tests
This test is intended to be used as an aid in the early diagnosis of RA and management of the disease.
Method Name
Enzyme-Linked Immunosorbent Assay (ELISA)
Reporting Name
14-3-3 eta, SSpecimen Type
Serum SSTSpecimen Minimum Volume
Serum: 0.4 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Serum SST | Refrigerated (preferred) | 14 days |
| Frozen | 100 days | |
| Ambient | 48 hours |
Reject Due To
| Gross hemolysis | Reject |
| Gross lipemia | Reject |
| Gross icterus | Reject |
Clinical Information
Serum 14-3-3 eta protein belongs to the 14-3-3 family of intracellular chaperone proteins (beta, gamma, epsilon, eta, sigma, theta, zeta). It is a joint-derived proinflammatory mediator that up-regulates cytokines and enzymes that perpetuate local and systemic inflammation and may contribute to joint damage.
Serum 14-3-3 eta is detectable at significantly higher levels in the serum from patients with rheumatoid arthritis (RA) when compared to healthy subjects and individuals with RA mimickers (other autoimmune conditions and viral/bacterial infections). It has also been reported as an important biomarker in diagnosing cases that are seronegative for traditional markers like rheumatoid factor (RF) and anti-citrullinated protein/peptide antibodies (ACPA).
In addition to the contribution of 14-3-3 eta in the diagnosis of RA, previous studies have reported its clinical potential of 14-3-3 eta as a predictor of poor clinical and radiographic outcomes, both at baseline and after initiation of treatment, even in Simplified Disease Activity Index (SDAI) remitters. These studies suggest that 14-3-3 eta, c-reactive protein, age, and ACPA represent independent predictors of subsequent joint damage.
Reference Values
< 0.19 ng/mL
Day(s) Performed
Wednesday
Report Available
3 to 9 daysPerforming Laboratory
Mayo Clinic Laboratories in Rochester
Test 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
83520