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Order Code LAB2327 Alpha-Fetoprotein (AFP), Spinal Fluid

Additional Codes

Mayo Test Code: AFPSF

Reporting Name

Alpha-Fetoprotein, CSF

Useful For

An adjunct in the diagnosis of central nervous system (CNS) germinomas and meningeal carcinomatosis

 

Evaluating the presence of germ-cell tumors in the CNS, in conjunction with cerebrospinal fluid (CSF) beta-human chorionic gonadotropin measurement

 

A supplement to CSF cytologic analysis

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Specimen Type

CSF


Specimen Required


Container/Tube: Sterile vial

Preferred: Vial number 1

Acceptable: Any vial

Specimen Volume: 1 mL


Specimen Minimum Volume

0.5 mL

Specimen Stability Information

Specimen Type Temperature Time
CSF Frozen (preferred) 7 days
  Refrigerated  7 days

Reference Values

<1.5 ng/mL

Values for alpha-fetoprotein in cerebrospinal fluid have not been formally established for newborns and infants. The available literature indicates that by 2 months of age, levels comparable to adults should be reached.(Ann Clin Biochem 2005;42:24-29)

Day(s) Performed

Monday through Saturday

CPT Code Information

86316

Method Description

The instrument used is a Beckman Coulter UniCel Dxl 800. The Access alpha-fetoprotein (AFP) immunoassay is a 2-site immunoenzymatic sandwich assay. The sample is added to a reaction vessel with mouse monoclonal anti-AFP alkaline phosphatase conjugate and paramagnetic particles coated with a second mouse monoclonal anti-AFP antibody. The AFP in the sample binds to the immobilized monoclonal anti-AFP on the solid phase, while the monoclonal anti-AFP-alkaline phosphatase conjugate reacts with different antigenic sites on the sample AFP. After incubation, materials bound to the solid phase are held in a magnetic field, while unbound materials are washed away. A chemiluminescence substrate is then added to the reaction vessel, and light generated by the reaction is measured with a luminometer. The light production is directly proportional to the amount of AFP in the sample. The amount of analyte in the sample is determined by means of a stored multipoint calibration curve. Because the protein matrix is less concentrated in cerebrospinal fluid, a "protein spike" is added to each specimen prior to analysis. Prior to reporting, a correction is made for the dilution effect.(Package insert: Access AFP. Beckman Coulter; 04/2020)

Reject Due To

Gross hemolysis Reject
Gross icterus OK

Method Name

Immunoenzymatic Assay

Forms

If not ordering electronically, complete, print, and send an Oncology Test Request (T729) with the specimen.