Ordering Recommendations

Preferred reflexive panel for diagnosing myasthenia gravis. Includes acetylcholine receptor (AChR) binding and blocking antibodies with reflex to AChR modulating antibodies.

Performed

Sun-Sat

Methodology

Quantitative Radioimmunoassay/Semi-Quantitative Flow Cytometry

Reported

3-7 days

Synonyms

  • AChR reflex panel
  • AChR Antibody
  • Myasthenia Gravis Antibodies Reflex
  • Myasthenia Gravis Antibodies
  • Muscle nicotinic Acetylcholine Receptor (AChR) Binding Antibody

Additional Technical Information

Performing Lab

Sendout Lab

CPT Codes

86041; 86042; if reflexed, add 86043

ARUP Test Code

2001571

Collect

Serum Separator Tube (SST).

Specimen Preparation

Separate from cells ASAP or within 2 hours of collection. Transfer 1 mL serum to an ARUP Standard Transport Tube. (Min: 0.5 mL)

Unacceptable Conditions

Contaminated, hemolyzed, or severely lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles)

Additional Technical Information

Reference Interval

Components
Reference Interval
Acetylcholine Binding Antibody0.4 nmol/L or less
Acetylcholine Blocking Antibody26 or less blocking

Interpretive Data

Approximately 85-90 percent of patients with myasthenia gravis (MG) express antibodies to the acetylcholine receptor (AChR), which can be divided into binding, blocking, and modulating antibodies. Binding antibody can activate complement and lead to loss of AChR. Blocking antibody may impair binding of acetylcholine to the receptor, leading to poor muscle contraction. Modulating antibody causes receptor endocytosis resulting in loss of AChR expression, which correlates most closely with clinical severity of disease. Approximately 10-15 percent of individuals with confirmed myasthenia gravis have no measurable binding, blocking, or modulating antibodies.

This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.

ComponentInterpretation
Acetylcholine Receptor Binding AntibodyNegative:
Positive:
0.0-0.4 nmol/L
0.5 nmol/L or greater
Acetylcholine Receptor Blocking AntibodyNegative:
Indeterminate:
Positive:
0-26% blocking
27-41% blocking
42% or greater blocking

Ordering

Ordering Recommendations

Preferred reflexive panel for diagnosing myasthenia gravis. Includes acetylcholine receptor (AChR) binding and blocking antibodies with reflex to AChR modulating antibodies.

Performed

Sun-Sat

Methodology

Quantitative Radioimmunoassay/Semi-Quantitative Flow Cytometry

Reported

3-7 days

Synonyms

  • AChR reflex panel
  • AChR Antibody
  • Myasthenia Gravis Antibodies Reflex
  • Myasthenia Gravis Antibodies
  • Muscle nicotinic Acetylcholine Receptor (AChR) Binding Antibody

Additional Technical Information

Performing Lab

Sendout Lab

CPT Codes

86041; 86042; if reflexed, add 86043

ARUP Test Code

2001571
Collection

Collect

Serum Separator Tube (SST).

Specimen Preparation

Separate from cells ASAP or within 2 hours of collection. Transfer 1 mL serum to an ARUP Standard Transport Tube. (Min: 0.5 mL)

Unacceptable Conditions

Contaminated, hemolyzed, or severely lipemic specimens.

Storage/Transport Temperature

Refrigerated.

Stability (from collection to initiation)

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles)

Additional Technical Information

Result Interpretation

Reference Interval

Components
Reference Interval
Acetylcholine Binding Antibody0.4 nmol/L or less
Acetylcholine Blocking Antibody26 or less blocking

Interpretive Data

Approximately 85-90 percent of patients with myasthenia gravis (MG) express antibodies to the acetylcholine receptor (AChR), which can be divided into binding, blocking, and modulating antibodies. Binding antibody can activate complement and lead to loss of AChR. Blocking antibody may impair binding of acetylcholine to the receptor, leading to poor muscle contraction. Modulating antibody causes receptor endocytosis resulting in loss of AChR expression, which correlates most closely with clinical severity of disease. Approximately 10-15 percent of individuals with confirmed myasthenia gravis have no measurable binding, blocking, or modulating antibodies.

This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.

ComponentInterpretation
Acetylcholine Receptor Binding AntibodyNegative:
Positive:
0.0-0.4 nmol/L
0.5 nmol/L or greater
Acetylcholine Receptor Blocking AntibodyNegative:
Indeterminate:
Positive:
0-26% blocking
27-41% blocking
42% or greater blocking