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AD Detect ® Beta-Amyloid 42/40 Ratio, P

Test Summary

Quest AD-Detect® Beta-Amyloid 42/40 Ratio, Plasma - This LC-MS/MS assay measures beta-amyloid 40 (AB40) as well as AB42 in plasma, rather than AB42 alone. This permits the normalization of beta amyloid levels circulating in plasma in different patients. Using the ratio of beta-amyloid 42/beta-amyloid 40, improves sensitivity and specificity for detecting Alzheimer's disease.

Aliases

  • ABeta 42,ABeta 40,AB40,AB42,Alzheimer's Disease (AD),AB42/40,AD,ABeta 42/40

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1.2 mL  plasma collected in an EDTA (lavender-top) tube. Plasma must be seperated from cells within 1 hour of collection. Frozen

Minimum Volume

0.6 mL

Instructions

Collect blood into an EDTA (lavender-top) tube and mix by inversion 10 times. Centrifuge to separate plasma from cells within 1 hour of collection. Carefully transfer plasma into a polypropylene tube. Do not transfer to conical tube. If unable to centrifuge within 1 hour of collection, store tube on ice.

Patient Preparation

N/A

Storage

Frozen

Transport Temperature

Frozen

Specimen Stability

  • Room Temperature: Unacceptable
  • Refrigerated: 72 hours Frozen -20° C: 32 days Frozen -70° C: 77 days

Limitations

N/A

Other Acceptable Specimens

N/A

Unacceptable Specimens

  • Moderate or gross hemolysis
  • Specimen collected in a glass, polystyrene, or polycarbonate tube

Order Code

ADBAR

EPIC (Premier) Code

LAB6918

Includes

ABeta 42, ABeta 40, ABeta 42/40 Ratio

CPT Code

  • 82233
  • 82234

Billing Code

  • 670292
  • 670352

CPT Statement

Methodology

Liquid Chromatography/Tandem Mass Spectrometry (LC/MS/MS)

FDA Status

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Physician Attestation of Informed Consent

N/A

Testing Laboratory

Quest Diagnostics Nichols Institute
33608 Ortega Highway
San Juan Capistrano CA, 92675

Reference Range

  • ABeta 42 Not established   pg/mL
  • ABeta 40 Not established  pg/mL
  • ABeta 42/40 Ratio ≥0.170

Setup Schedule / Expected Turnaround Time

Monday - Saturday; Report available: 3 - 5 days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1.2 mL  plasma collected in an EDTA (lavender-top) tube. Plasma must be seperated from cells within 1 hour of collection. Frozen

Minimum Volume

0.6 mL

Instructions

Collect blood into an EDTA (lavender-top) tube and mix by inversion 10 times. Centrifuge to separate plasma from cells within 1 hour of collection. Carefully transfer plasma into a polypropylene tube. Do not transfer to conical tube. If unable to centrifuge within 1 hour of collection, store tube on ice.

Patient Preparation

N/A

Storage

Frozen

Transport Temperature

Frozen

Specimen Stability

  • Room Temperature: Unacceptable
  • Refrigerated: 72 hours Frozen -20° C: 32 days Frozen -70° C: 77 days

Limitations

N/A

Other Acceptable Specimens

N/A

Unacceptable Specimens

  • Moderate or gross hemolysis
  • Specimen collected in a glass, polystyrene, or polycarbonate tube

Billing

CPT Code

  • 82233
  • 82234

Billing Code

  • 670292
  • 670352

CPT Statement

Result Information

Methodology

Liquid Chromatography/Tandem Mass Spectrometry (LC/MS/MS)

Testing Laboratory

N/A

Reference Range

  • ABeta 42 Not established   pg/mL
  • ABeta 40 Not established  pg/mL
  • ABeta 42/40 Ratio ≥0.170

Setup Schedule / Expected Turnaround Time

Monday - Saturday; Report available: 3 - 5 days