Time for optimism in amyotrophic lateral sclerosis

Author:

Corcia Philippe12ORCID,Lunetta Christian3,Vourc'h Patrick24,Pradat Pierre‐François567,Blasco Hélène27

Affiliation:

1. CRMR SLA CHU Tours Tours France

2. UMR1253 iBrain UMR Université de Tours, INSERM Tours France

3. ALS Unit, IRCCS Istituti Clinici Scientifici Maugeri Milan Italy

4. Laboratoire de Biochimie et Biologie Moléculaire CHRU de Tours Tours France

5. CNRS, INSERM, Laboratoire d'Imagerie Biomédicale Sorbonne Université Paris France

6. Département de Neurologie, Hôpital Pitié‐Salpêtrière, Centre référent SLA APHP Paris France

7. Northern Ireland Centre for Stratified Medicine Biomedical Sciences Research Institute, Ulster University, C‐TRIC, Altnagelvin Hospital Derry/Londonderry UK

Abstract

AbstractBackground and purposeAmyotrophic lateral sclerosis (ALS) is among the most common motor neuron diseases in adults. Nevertheless, ALS remains fatal, despite decades of research and clinical trials, which has led to negative conclusions until recently in regard to four specific treatments. It is well known that we can learn from failures, and we consider that the time has come to present positive insight on this disease.MethodsWe did a literature search using PubMed and Scopus for articles published in English from 1 January 2016, to 30 June 2022 dealing with “amyotrophic lateral sclerosis”, diagnosis, treatment, and biomarkers.ResultsA comprehensive review of the literature on diagnosis, monitoring, and treatment of this condition showed convincing evidence that we are now able to diagnose earlier as well as to better monitor and treat ALS.ConclusionsAlthough ALS is often difficult to diagnose and remains incurable, there are many indications that an optimistic view of ALS management in the coming years is now realistic.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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