Serum neurofilament light levels in normal aging and their association with morphologic brain changes
Open accessAbstract
Neurofilament light (NfL) protein is a marker of neuro-axonal damage and can be measured not only in cerebrospinal fluid but also in serum, which allows for repeated assessments. There is still limited knowledge regarding the association of serum NfL (sNfL) with age and subclinical morphologic brain changes and their dynamics in the normal population. We measured sNfL by a single molecule array (Simoa) assay in 335 individuals participating in a population-based cohort study and after a mean follow-up time of 5.9 years (n = 103). Detailed clinical examination, cognitive testing and 3T brain MRI were performed to assess subclinical brain damage. We show that rising and more variable sNfL in individuals >60 years indicate an acceleration of neuronal injury at higher age, which may be driven by subclinical comorbid pathologies. This is supported by a close association of sNfL with brain volume changes in a cross-sectional and especially longitudinal manner.
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Inter-assay validity results are comparable to another large study investigating NfL and reporting assay precision.
“We provide data for inter-assay validity and found those results comparable to another large study investigating NfL and reporting assay precision15.”
From Seven day pre-analytical stability of serum and plasma neurofilament light chain (2021) · cites this paper as [15]
Reference values for serum NfL have already been reported.
“We decided to present formulas to calculate serum NfL from EDTA-plasma NfL because reference values for serum NfL have already been reported (29).”
From A Method to Combine Neurofilament Light Measurements From Blood Serum and Plasma in Clinical and Population-Based Studies (2022) · cites this paper as [29]
We derived a formula to convert values from EDTA-plasma NfL to serum NfL.
“We derived a formula to convert values from EDTA-plasma NfL to serum NfL so that reference values for serum NfL (29) can also be applied if only EDTA-plasma NfL is available.”
From A Method to Combine Neurofilament Light Measurements From Blood Serum and Plasma in Clinical and Population-Based Studies (2022) · cites this paper as [29]
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“We derived a formula to convert values from EDTA-plasma NfL to serum NfL so that reference values for serum NfL (29) can also be applied if only EDTA-plasma NfL is available.”
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Neurofilament light level correlates with brain atrophy, and cognitive and motor performance
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- Authors
- Khalil, M., Pirpamer, L., Hofer, E., Voortman, M. M., Barro, C., Leppert, D., Benkert, P., Ropele, S., Enzinger, C., Fazekas, F., Schmidt, R., & Kuhle, J.
- Affiliations
- Medical University of Graz (AT)
- University of Basel (CH)
- Corresponding author
- Khalil, Michael
- ORCID
- Venue
- Nature Communications
- Published
- 2020-02-10
- Volume
- 11
- Issue
- 1
- Pages
- 812-812
- ISSN
- 2041-1723 (ISSN-L)
- PMC
- PMC7010701
- OpenAlex
- W3004767455
- Cited by
- 572
- References
- 3
- Citations by year
- 2026: 59 · 2025: 88 · 2024: 120 · 2023: 105 · 2022: 100 · 2021: 75 · 2020: 23
- FWCI
- 55.27
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Nature Communications (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Research Foundation
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Neurology › Cerebrovascular and genetic disorders
- Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
- Keywords
- serum neurofilament light, normal aging, brain volume changes, neuroaxonal damage, brain MRI, cognitive decline, comorbid pathology
- MeSH terms
- Adult, Aged, Aged, 80 and over, Aging, Atrophy, Brain, Cognition, Cross-Sectional Studies, Female, Humans, Longitudinal Studies, Magnetic Resonance Imaging, Male, Middle Aged, Biomarkers, Neurofilament Proteins, Leukoencephalopathies
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