Acetylcholine Receptor Antibodies with MuSK Reflex by RIPA, Serum; test site BCN
Test Overview
Clinical Utility
Myasthenia gravis (MG) is an autoimmune disorder that leads to weakness and diminished control over voluntary muscles. It results from reduced signaling in the neuromuscular junction (NMJ) that connects nerves to muscle fibers. Typically, the areas of reduced functioning are the muscles of the eyes, face, and throat. There are three types of acquired MG: ocular (OMG), bulbar predominant (BMG), and generalized (GMG).
In MG, the body produces antibodies (Ab) that bind with receptors in the NMJ, blocking or destroying them, thereby preventing chemical signaling from the brain to the muscles.
The majority of cases (about 85%) of MG are caused by autoantibodies targeting the acetylcholine receptors (AChR). Approximately 6% of cases are caused by autoantibodies targeting the extracellular domain of muscle specific tyrosine-kinase (MuSK) receptors. Amongst the approximately 15% of cases of MG that are found to be AChR Ab-negative, however, MuSK Abs have been reported in patients with frequencies ranging from 0 – 64%, depending on ethnic group and geographic location.
The remaining cases are considered double-seronegative MG, as the patients sera appears negative for both AChR and MuSK antibodies. These cases can be caused by autoantibodies to a variety of other proteins, including but not limited to lipoprotein-related protein 4 (LRP4), agrin, and cortactin.
Method
Radioimmunoprecipitation Assay (RIPA)
Method Description
Acetylcholine Receptor (AChR) Antibodies: This radioimmunoprecipitation assay (RIPA) uses a double antibody precipitation technique using the Kronus antigen, a genetically engineered acetylcholine receptor to assess presence of myasthenia gravis-related autoantibodies.
BC Neuroimmunology offers two AChR antibody RIPA protocols, qualitative and quantitative. All positive qualitative assays are repeated using the quantitative assay to permit comparison of titres and results reported as nanomoles of Human Acetylcholine Receptors precipitated by 1 litre of serum (nmol/L).
MuSK testing is performed after AchR Ab testing and will not be done if the patient is AchR Ab positive.
Result Included
Acetylcholine Receptor Antibodies RIPA Screen; Acetylcholine Receptor Antibodies RIPA Quantitation; MuSK RIPA Screen
Aliases/Synonyms
AChR; AChRAB; ACRAB; anti-AchR Ab; Myasthenia gravis (MG) autoantibodies; Muscle-specific Tyrosine Kinase; Muscle Specific Tyrosine Kinase
Specimen
Specimen Type
SerumContainers
Collection Containers
Gold top (SST)
Volume
Sample Volume
5 mL
Minimum Volume
1 mL
Patient Preparation
Please indicate if patient is on or has recently had IVIG treatment.
Collection & Handling
Handling Information
Store and send frozen (preferred).
Stability
| Refrigerated | Frozen |
|---|---|
| 7 days | 30 days |
If the specimen thaws, it is unsuitable for analysis.
Performance & Interpretation
Turnaround Time
30 days
Results
-
Acetylcholine Receptor Antibodies Screen by RIPA
-
Acetylcholine Receptor Antibodies by RIPAnmol/LAbsent: <0.2
Borderline: 0.2 - 2.0
Positive Low: 2 - 5
Positive Medium: 5 - 10
Positive High: >10 -
MuSK Ab by RIPA
Referral Location
Canada
Interface & Setup
HL7 Interface Codes
| Order Code | Result Name | Result Codes | Units |
|---|---|---|---|
| <a href="https://iclabs.ca/wp-content/uploads/icl-test-attachments/ACMKR%20S%20-%20HL7%20Codes.pdf" target="_blank">View HL7 Codes</a> |
Test Version
Last Updated
2025-03-03