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Myelin Oligodendrocyte Glycoprotein (MOG) Antibody, CBA with Reflex to Titer
Test Code37134
CPT Codes
86255<br /> Limited Access Code
Physician Attestation of Informed Consent
This germline genetic test requires physician attestation that patient consent has been received if ordering medical facility is located in AK, DE, FL, GA, IA, MA, MN, NV, NJ, NY, OR, SD or VT or test is performed in MA.
Includes
If the MOG Antibody, CBA is positive a semi-quantitative titer will be performed at an additional charge (CPT code 86256).
Preferred Specimen
2 mL serum
Minimum Volume
0.5 mL
Other Acceptable Specimens
CSF collected in a plastic screw-cap vial
Instructions
Serum must be separated from whole blood within 48 hours of collection. Please label each specimen tube with two forms of patient identification. These forms of identification must also appear on the requisition form.
Transport Temperature
Refrigerated (cold packs)
Specimen Stability
Room temperature: 72 hours
Refrigerated: 45 days
Frozen: 39 days
Refrigerated: 45 days
Frozen: 39 days
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Turbid and/or any suggestion of bacterial contamination is present
Methodology
Cell-based Immunofluorescence Assay
FDA Status
This test was developed and its analytical performance characteristics have been determined by Athena Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
Setup Schedule
Set up: As needed; Report available: 3-7 days
Reference Range
See Laboratory Report
Clinical Significance
Neuromyelitis optica (NMO) is an inflammatory disorder predominantly affecting the optic nerves and spinal cord. Limited forms of disease including isolated optic neuritis, brainstem encephalitis and longitudinal extensive transverse myelitis (LETM) or acute disseminated encephalomyelitis (ADEM) have been referred to as NMO spectrum disorder (NMOSD). The majority of individuals with NMO and many with NMOSD have antibodies against aquaporin-4 (AQP4). MOG antibodies have been reported without AQP4 antibodies in individuals with NMO and other non-multiple sclerosis demyelinating diseases. The presence of MOG antibodies in AQP4 antibody negative individuals can help differentiate between multiple sclerosis (MS) and non-MS demyelinating diseases and aid in clinical management decisions.