Ordering Recommendations

Assessment of clinical activity of and initial diagnostic testing for myasthenia gravis. For reflexive panel, which contains binding, blocking, and modulating antibodies, refer to Acetylcholine Receptor Antibody Reflexive Panel (2001571).

Collect

Serum Separator Tube (SST).

Specimen Preparation

Separate from cells ASAP or within 2 hours of collection. Transfer 0.5 mL serum to an ARUP Standard Transport Tube. (Min: 0.3 mL)

Storage/Transport Temperature

Refrigerated.

Unacceptable Conditions

Contaminated, hemolyzed, or severely lipemic specimens.

Stability (from collection to initiation)

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

Referral Lab

Lab Section

Send-out Lab

Performing Lab

ARUP Laboratories

Methodology

Semi-Quantitative Flow Cytometry

Performed

Sun-Fri

Reported

2-7 days

Synonyms

  • Myasthenia Gravis Antibodies (Acetylcholine Receptor Modulating Antibody)
  • Muscle nicotinic Acetylcholine Receptor (AChR) Modulating Antibody
  • Myasthenia Gravis Antibodies
  • ACHR modulating antibody
  • AChR Antibody

Additional Technical Information

Reference Interval

Components
Reference Interval
Acetylcholine Modulating Antibody45 or less modulating

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.

Component
Interpretation
Acetylcholine Receptor Modulating AntibodyNegative:  0-45% modulating
Positive:  46% or greater modulating

CPT Codes

86043

LOINC

  • 30192-9

Order Type (Individual or Group)

I

Result Test ID

ACRM

Reportable?

Y

Result Test Name

ACETYLCHOLINE REC MOD AB

Result Type (Individual or Group)

I

Type (Alpha or Numeric)

N

Text

SEPARATE FROM CELLS WITHIN 2 HOURS

CPT Codes

86043

LOINC

  • 30192-9

Pricing

Refer to Lab Account Manager. email: labservicesoutreach@urmc.rochester.edu
Specimen Requirements

Ordering Recommendations

Assessment of clinical activity of and initial diagnostic testing for myasthenia gravis. For reflexive panel, which contains binding, blocking, and modulating antibodies, refer to Acetylcholine Receptor Antibody Reflexive Panel (2001571).

Collect

Serum Separator Tube (SST).

Specimen Preparation

Separate from cells ASAP or within 2 hours of collection. Transfer 0.5 mL serum to an ARUP Standard Transport Tube. (Min: 0.3 mL)

Storage/Transport Temperature

Refrigerated.

Unacceptable Conditions

Contaminated, hemolyzed, or severely lipemic specimens.

Stability (from collection to initiation)

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

Referral Lab

Testing

Lab Section

Send-out Lab

Performing Lab

ARUP Laboratories

Methodology

Semi-Quantitative Flow Cytometry

Performed

Sun-Fri

Reported

2-7 days

Synonyms

  • Myasthenia Gravis Antibodies (Acetylcholine Receptor Modulating Antibody)
  • Muscle nicotinic Acetylcholine Receptor (AChR) Modulating Antibody
  • Myasthenia Gravis Antibodies
  • ACHR modulating antibody
  • AChR Antibody

Additional Technical Information

Result Interpretation

Reference Interval

Components
Reference Interval
Acetylcholine Modulating Antibody45 or less modulating

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.

Component
Interpretation
Acetylcholine Receptor Modulating AntibodyNegative:  0-45% modulating
Positive:  46% or greater modulating

Coding

CPT Codes

86043

LOINC

  • 30192-9
URM Labs Internal
Test Build

Order Type (Individual or Group)

I

Result Test ID

ACRM

Reportable?

Y

Result Test Name

ACETYLCHOLINE REC MOD AB

Result Type (Individual or Group)

I

Type (Alpha or Numeric)

N

Text

SEPARATE FROM CELLS WITHIN 2 HOURS

CPT Codes

86043

LOINC

  • 30192-9

Pricing

Refer to Lab Account Manager. email: labservicesoutreach@urmc.rochester.edu