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Test Directory

Acylcarnitine, Plasma

Test Summary

Determining the specific apolipoprotein E (APOE) genotypes in individuals with type III hyperlipoproteinemia. Determining the specific apolipoprotein E (APOE) genotypes that may increase risk for amyloid related imaging abnormalities in individuals being treated for Alzheimer disease with B-amyloid-targeting antibodies. APOE genotyping has been used to assess susceptibility for Alzheimer disease. However, the use of APOE analysis for predictive testing for Alzheimer disease is not currently recommended by the American College of Medical Genetics due to limited clinical utility and poor predictive value.

Aliases

  • N/A

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1 mL frozen plasma collected in sodium heparin (green-top) tube

Minimum Volume

0.5 mL frozen serum

Instructions

Collect blood sample in sodium heparin (green-top) tube. Separate plasma by centrifugation ASAP. Avoid hemolysis. Remove plasma and place in plastic tube. Freeze immediately after separation. Date of birth is required.

Patient Preparation

Patient should be in a well-fed state

Storage

N/A

Transport Temperature

Frozen

Specimen Stability

  • Room Temperature = Unacceptable
  • Refrigerated = Unacceptable
  • Frozen = 28 days

Limitations

A low carnitine level may mask a disease state.

Other Acceptable Specimens

Serum

Unacceptable Specimens

Gross hemolysis • Received room temperature • Received refrigerated

Order Code

ACYLCP

EPIC (Premier) Code

LAB6018

Includes

N/A

CPT Code

  • 82017

Billing Code

  • 700000

CPT Statement

Methodology

Chromatography/Mass Spectrometry

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 the U.S. Food and Drug Administration. The FDA has determined that such clearance or approval is not necessary. 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

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Mornings; 3 days a week. Report available: 5 - 6 days.

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1 mL frozen plasma collected in sodium heparin (green-top) tube

Minimum Volume

0.5 mL frozen serum

Instructions

Collect blood sample in sodium heparin (green-top) tube. Separate plasma by centrifugation ASAP. Avoid hemolysis. Remove plasma and place in plastic tube. Freeze immediately after separation. Date of birth is required.

Patient Preparation

Patient should be in a well-fed state

Storage

N/A

Transport Temperature

Frozen

Specimen Stability

  • Room Temperature = Unacceptable
  • Refrigerated = Unacceptable
  • Frozen = 28 days

Limitations

A low carnitine level may mask a disease state.

Other Acceptable Specimens

Serum

Unacceptable Specimens

Gross hemolysis • Received room temperature • Received refrigerated

Billing

CPT Code

  • 82017

Billing Code

  • 700000

CPT Statement

Result Information

Methodology

Chromatography/Mass Spectrometry

Testing Laboratory

N/A

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Mornings; 3 days a week. Report available: 5 - 6 days.