Test Code 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.
Specimen Stability Information: Frozen (preferred) 16 months/Refrigerated 7 days
Useful 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 | Special Container |
---|---|---|---|
Plasma EDTA | Frozen (preferred) | ||
Refrigerated | 7 days |
Reject Due To
Gross hemolysis | Reject |
Gross lipemia | OK |
Gross icterus | OK |
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 neurodegenerative 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. Concentrations of NfL in plasma have been shown to be approximately 5% to 10% lower than those measured in serum.
Circulating NfL concentrations increase with age with reported increases of approximately 2% to 3% per year in both male and female individuals. While the specific cause of this increase has not been elucidated, it is believed to be related to the aging process as well as to the development of subclinical ischemic events. NfL concentrations in blood (plasma or serum) 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
<2.5 years: ≤12.8 pg/mL
2.5 to 4 years: ≤11.8 pg/mL
5 to 9 years: ≤10.4 pg/mL
10 to 14 years: ≤8.8 pg/mL
15 to 19 years: ≤9.2 pg/mL
20 to 24 years: ≤10.4 pg/mL
25 to 29 years: ≤11.9 pg/mL
30 to 34 years: ≤13.5 pg/mL
35 to 39 years: ≤15.3 pg/mL
40 to 44 years: ≤17.3 pg/mL
45 to 49 years: ≤19.7 pg/mL
50 to 54 years: ≤22.4 pg/mL
55 to 59 years: ≤25.4 pg/mL
60 to 64 years: ≤28.8 pg/mL
65 to 69 years: ≤32.7 pg/mL
70 to 74 years: ≤37.1 pg/mL
75 to 79 years: ≤42.1 pg/mL
80 to 84 years: ≤ 47.8 pg/mL
≥85 years: ≤54.3 pg/mL
Day(s) Performed
Monday, Wednesday, Friday
Report Available
1 to 7 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest 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
Forms
If not ordering electronically, complete, print, and send a Neurology Specialty Testing Client Test Request (T732) with the specimen.