Biofluid Biomarkers in the Prognosis of Amyotrophic Lateral Sclerosis: Recent Developments and Therapeutic Applications
- PMID: 37190090
- PMCID: PMC10136823
- DOI: 10.3390/cells12081180
Biofluid Biomarkers in the Prognosis of Amyotrophic Lateral Sclerosis: Recent Developments and Therapeutic Applications
Abstract
Amyotrophic lateral sclerosis is a neurodegenerative disease characterized by the degeneration of motor neurons for which effective therapies are lacking. One of the most explored areas of research in ALS is the discovery and validation of biomarkers that can be applied to clinical practice and incorporated into the development of innovative therapies. The study of biomarkers requires an adequate theoretical and operational framework, highlighting the "fit-for-purpose" concept and distinguishing different types of biomarkers based on common terminology. In this review, we aim to discuss the current status of fluid-based prognostic and predictive biomarkers in ALS, with particular emphasis on those that are the most promising ones for clinical trial design and routine clinical practice. Neurofilaments in cerebrospinal fluid and blood are the main prognostic and pharmacodynamic biomarkers. Furthermore, several candidates exist covering various pathological aspects of the disease, such as immune, metabolic and muscle damage markers. Urine has been studied less often and should be explored for its possible advantages. New advances in the knowledge of cryptic exons introduce the possibility of discovering new biomarkers. Collaborative efforts, prospective studies and standardized procedures are needed to validate candidate biomarkers. A combined biomarkers panel can provide a more detailed disease status.
Keywords: amyotrophic lateral sclerosis (ALS); biomarker; genetics; neurofilament light (NfL) protein; neuroinflammation; pharmacodynamic biomarker; prognosis.
Conflict of interest statement
R.J.-M. and J.M.V.T. has received research grants from “Instituto de Salud Carlos III” and European Regional Development Fund: “A way to make Europe“. R.J.-M. was involved as site principal investigator for the following clinical trial sponsors: Orphazyme, PTC Therapeutics, Sanofi, Apellis Pharmaceuticals, Transposon Therapeutics, Corcept Therapeutics and Alexion. The other authors declare no conflicts of interest.
References
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