Aid in diagnosis of contactin associated protein 2 (CASPR2) antibody disorders associated with acquired neuromyotonia, limbic encephalitis, painful neuropathy, and Morvan syndrome. Use to manage antibody-positive (CASPR2) individual following immunotherapy and/or plasmapheresis.
Specimen Sources
Blood, ArterialBlood, CapillaryBlood, Central LineBlood, Venous
Specimen Types
Blood
Container
Gold Top Tube
Collection Instructions
Container/Tube: Gold top tube Specimen: 1 mL serum (0.2mL min) Transport Temperature: Refrigerated
Specimen Volume
1 mL serum (0.2mL min)
Transport Instructions
Refrigerated
Specimen Stability
Methodology
Semi-Quantitative Indirect Fluorescent Antibody
Days Performed
Wednesdays
TAT 2 - 9 days
Performing Laboratory
ARUP Laboratories
CPT
86255 If reflexed add 86256
LOINC: 82979-6
PDM
1759245
Only Orderable at Locations:
Orderable Everywhere
Results
Component Name
Base Name
Common Name
External Name
CASPR2 AB IGG SCREEN BY IFA
CASPR2
CASPR2 AB IGG SCREEN BY IFA
CASPR2 Ab IgG Screen by IFA
CASPR2 AB IGG TITER BY IFA
CASPR2
CASPR2 AB IGG TITER BY IFA
CASPR2 Ab IgG Titer by IFA
Result Interpretation
Less than 1:10
Contactin-associated protein-2 (CASPR2) IgG antibody may occur
as part of the voltage-gated potassium channel (VGKC) complex
antibodies.
The presence of CASPR2 IgG antibody is associated with a wide
spectrum of clinical manifestations, including acquired
neuromyotonia, limbic encephalitis, painful neuropathy and Morvan
syndrome. Tumors such as thymoma, small-cell lung cancer, and other
rarer tumors may occur. The full-spectrum of clinical disorders and
tumors associated with the CASPR2 IgG antibody continues to be
defined. Results should be interpreted in correlation with the
patient's clinical history and other laboratory findings.
This indirect fluorescent antibody assay utilizes
contactin-associated protein-2 (CASPR2) transfected cell lines for
the detection and semi-quantification of the CASPR2 IgG
antibody
This test was developed and its performance characteristics
determined by ARUP Laboratories. The U. S. Food and Drug
Administration has not approved or cleared this test; however, FDA
clearance or approval is not currently required for clinical use.
The results are not intended to be used as the sole means for
clinical diagnosis or patient management decisions