Visual outcome measures in clinical trials of remyelinating drugs.

CLINICAL NEUROLOGY MULTIPLE SCLEROSIS MYELIN NEUROOPHTHALMOLOGY VISUAL EVOKED POTENTIALS

Journal

BMJ neurology open
ISSN: 2632-6140
Titre abrégé: BMJ Neurol Open
Pays: England
ID NLM: 101775450

Informations de publication

Date de publication:
2024
Historique:
received: 16 10 2023
accepted: 15 01 2024
medline: 23 2 2024
pubmed: 23 2 2024
entrez: 23 2 2024
Statut: epublish

Résumé

One of the most promising approaches to delay, prevent or reverse disability progression in multiple sclerosis (MS) is to enhance endogenous remyelination and limit axonal degeneration. In clinical trials of remyelinating drugs, there is a need for reliable, sensitive and clinically relevant outcome measures. The visual pathway, which is frequently affected by MS, provides a unique model system to evaluate remyelination of acute and chronic MS lesions in vivo and non-invasively. In this review, we discuss the different measures that have been used and scrutinise visual outcome measure selection in current and future remyelination trials.

Identifiants

pubmed: 38389586
doi: 10.1136/bmjno-2023-000560
pii: bmjno-2023-000560
pmc: PMC10882304
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

e000560

Informations de copyright

© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: Gioia Riboni-Verri, Benson S Chen, Christopher E McMurran, Gregory J Halliwell and Nick Cunniffe declare they have no financial interests. J William L Brown received speaking fees, consulting fees and travel support from Biogen, Novartis and Roche. Alasdair J Coles received grant support, honoraria and travel support from Sanofi up until September 2017. Nil since.

Auteurs

Gioia Riboni-Verri (G)

Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Cambridge Clinical Vision Laboratory, University of Cambridge, Cambridge, UK.

Benson S Chen (BS)

Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Cambridge Clinical Vision Laboratory, University of Cambridge, Cambridge, UK.

Christopher E McMurran (CE)

Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Cambridge Clinical Vision Laboratory, University of Cambridge, Cambridge, UK.
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.

Gregory J Halliwell (GJ)

Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.

J William L Brown (JWL)

Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Clinical Outcomes Research Unit (CORe), University of Melbourne, Melborune, Melborune, Australia.

Alasdair J Coles (AJ)

Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Cambridge Clinical Vision Laboratory, University of Cambridge, Cambridge, UK.

Nick G Cunniffe (NG)

Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Cambridge Clinical Vision Laboratory, University of Cambridge, Cambridge, UK.

Classifications MeSH