Test ID NFLC Neurofilament Light Chain, Plasma
Specimen Required
Collection Container/Tube: Lavender top (EDTA)
Submission Container/Tube: Plastic screw-top vial
Specimen Volume: 1.5 mL
Collection Information: Centrifuge and aliquot plasma into a plastic vial. Do not submit specimen in original tube.
Forms
If not ordering electronically, complete, print, and send a Neurology Specialty Testing Client Test Request (T732) with the specimen.
Secondary ID
616854Useful For
Assessing neuronal damage related to various neurodegenerative diseases
Method Name
Digital Immunoassay
Reporting Name
Neurofilament Light Chain, PSpecimen Type
Plasma EDTASpecimen Minimum Volume
0.75 mL
Specimen Stability Information
Specimen Type | Temperature | Time |
---|---|---|
Plasma EDTA | Frozen (preferred) | 90 days |
Refrigerated | 7 days |
Clinical Information
Neurofilaments (NF) are exclusively located in the neuronal cytoskeleton and are released to the interstitial fluid upon axonal injury or neurodegeneration. NF concentrations in cerebrospinal fluid (CSF) and blood have been shown to correlate with the extent of axonal damage or neurodegeneration in various diseases. Of the family of NF proteins, neurofilament light chain (NfL) has gained the most interest as a candidate marker of neurodegeneration. During axonal damage, NfL is released into the CSF, and eventually into the blood where concentrations are 40-fold lower than in the CSF. NfL concentrations increase with age with a reported increase in healthy control of 2.2% per year. While the specific cause of this increase has not been elucidated, it is believed to be related to aging itself as well as to the development of subclinical ischemic events. NfL concentrations in blood reflect the extent of axonal damage, making them a generic marker of disease activity. Increases in NfL concentrations have been reported in individuals with traumatic brain injury, amyotrophic lateral sclerosis, multiple sclerosis, frontotemporal dementia, Alzheimer disease, and other neurodegenerative diseases.
Reference Values
<20 years: Not established
20 to 29 years: ≤8.4 pg/mL
30 to 39 years: ≤11.4 pg/mL
40 to 49 years: ≤15.4 pg/mL
50 to 59 years: ≤20.8 pg/mL
60 to 69 years: ≤28.0 pg/mL
70 to 79 years: ≤37.9 pg/mL
≥80 years: ≤51.2 pg/mL
Cautions
Increases in neurofilament light chain (NfL) are not disease specific. Results should only be used in conjunction with other clinical information when evaluating patients with neurodegeneration.
Higher concentrations of NfL may be found in persons with history of stroke, atrial fibrillation, myocardial infarction, chronic kidney disease, pregnancy, and diabetes.
Lower concentrations of NfL may be found in individuals who are obese (BMI ≥30).
All immunometric assays can, on rare occasions, be subject to a hooking effect at extremely high analyte concentrations (false-low results), heterophilic antibody interference (false-high results), or autoantibody interference (unpredictable effects). If the laboratory result does not fit the clinical picture, these possibilities should be considered.
Day(s) Performed
Monday, Thursday
Report Available
1 to 7 daysPerforming Laboratory

Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
0361U