Immunoglobulin G Synthesis Rate, Cerebrospinal Fluid
Use
The Cerebrospinal Fluid IgG Synthesis Rate test evaluates the production rate of Immunoglobulin G (IgG) in the central nervous system (CNS). It is primarily used to diagnose inflammatory and autoimmune diseases affecting the CNS, such as multiple sclerosis. The test calculates the IgG synthesis rate using measurements of IgG and albumin in both serum and spinal fluid. It helps in determining whether increased levels of IgG in the CNS are due to local synthesis or systemic elevations followed by passive transfer across the blood-brain barrier.
Special Instructions
The test employs an empirically-derived formula, validated through radiolabeled experiments, to estimate IgG production by the CNS. The process takes into account the ratio of average normal serum IgG to CSF IgG. An intact blood-brain barrier is assumed in this calculation, which is noted in the formula applied for synthesizing data.
Limitations
The validity of the IgG synthesis formula is dependent on the assumption that an intact blood-brain barrier governs the proportion of IgG passing into the CSF. The test results must be correlated with clinical findings as the diagnosis of diseases like multiple sclerosis remains a clinical neurologic one. There can be cases where the CNS IgG synthesis rate is normal even in the presence of neurological conditions, therefore sensitivity and specificity metrics should be evaluated alongside clinical contexts.
Methodology
Immunoassay
Biomarkers
LOINC Codes
- 2464-6
- 1746-7
- 1751-7
- 2465-3
- 14116-8
Result Turnaround Time
3-6 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
1.5 mL
Minimum Volume
0.7 mL
Container
Red-top tube or gel-barrier tube
Storage Instructions
Room temperature
Causes for Rejection
Blood in CSF; failure to obtain blood and CSF specimens
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 14 days |
| Refrigerated | 14 days |
| Frozen | 14 days |
