Update on recent advances in amyotrophic lateral sclerosis
- PMID: 38802624
- PMCID: PMC11233360
- DOI: 10.1007/s00415-024-12435-9
Update on recent advances in amyotrophic lateral sclerosis
Abstract
In the last few years, our understanding of disease molecular mechanisms underpinning ALS has advanced greatly, allowing the first steps in translating into clinical practice novel research findings, including gene therapy approaches. Similarly, the recent advent of assistive technologies has greatly improved the possibility of a more personalized approach to supportive and symptomatic care, in the context of an increasingly complex multidisciplinary line of actions, which remains the cornerstone of ALS management. Against this rapidly growing background, here we provide an comprehensive update on the most recent studies that have contributed towards our understanding of ALS pathogenesis, the latest results from clinical trials as well as the future directions for improving the clinical management of ALS patients.
Keywords: ALS genetics; Assistive devices; Clinical management; Gene therapy; Motor neuron disease; Neuroimaging; Pathogenesis.
© 2024. The Author(s).
Conflict of interest statement
On behalf of all the authors, the corresponding author states that there is no conflict of interest.
References
-
- Al-Chalabi A, Hardiman O. The epidemiology of ALS: a conspiracy of genes, environment and time. Nat Rev Neurol. 2013;9:617–628. - PubMed
-
- Xu L, Liu T, Liu L, Yao X, Chen L, Fan D, Zhan S, Wang S. Global variation in prevalence and incidence of amyotrophic lateral sclerosis: a systematic review and meta-analysis. J Neurol. 2020;267:944–953. - PubMed
-
- Lloyd-Sherlock P. Population ageing in developed and developing regions: implications for health policy. Soc Sci Med. 2000;51:887–895. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous