touchMEETING HIGHLIGHTS
Pioneering pathways: evolving use of neurofilaments in neurodegenerative disease
Overview
Neurofilaments, the building blocks of neurons are released into the cerebrospinal fluid and blood by injured and degenerating neurons.1,2 In the neurological diseases, amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy (SMA), neurofilament levels are elevated and can be measured.3,4 In this activity, learn about the relationship between neurofilament levels and disease progression in ALS and SMA, and the potential use of neurofilament levels in trials and clinical practice.
Learning Objectives
After watching this activity, participants should be better able to:
- Educate on the foundation of evidence for potential use of neurofilaments in understanding biological and pathogenic processes and/or response
- Discuss the evolving paradigm of use of neurofilaments in clinical research of neurodegenerative disease
- Discuss considerations for use of neurofilaments in SMA and ALS clinical practice
References
- Yuan A, Rao MV, Veeranna, et al. Neurofilaments and Neurofilament Proteins in Health and Disease. Cold Spring Harb Perspect Biol. 2017;9(4):a018309.
- Verde F, Otto M, Silani V. Neurofilament Light Chain as Biomarker for Amyotrophic Lateral Sclerosis and Frontotemporal Dementia. Front Neurosci. 2021;15:679199.
- Witzel S, Huss A, Nagel G, et al. Population-Based Evidence for the Use of Serum Neurofilaments as Individual Diagnostic and Prognostic Biomarkers in Amyotrophic Lateral Sclerosis. Ann Neurol. 2024;96(6):1040-1057.
- Bayoumy S, Verberk IMW, Vermunt L, et al. Neurofilament light protein as a biomarker for spinal muscular atrophy: a review and reference ranges. Clin Chem Lab Med. 2024;62(7):1252-1265.
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