A2 Refereed review article in a scientific journal
Neuroimaging to monitor worsening of multiple sclerosis : advances supported by the grant for multiple sclerosis innovation
Authors: Oh Jiwon, Airas Laura, Harrison Daniel, Järvinen Elina, Livingston Terrie, Lanker Stefan, Malik Rayaz A., Okuda Darin T., Villoslada Pablo, de Vries Helga E.
Publisher: Frontiers Media
Publication year: 2023
Journal: Frontiers in Neurology
Journal name in source: FRONTIERS IN NEUROLOGY
Journal acronym: FRONT NEUROL
Article number: 1319869
Volume: 14
ISSN: 1664-2295
eISSN: 1664-2295
DOI: https://doi.org/10.3389/fneur.2023.1319869
Web address : https://www.frontiersin.org/articles/10.3389/fneur.2023.1319869/full
Self-archived copy’s web address: https://research.utu.fi/converis/portal/detail/Publication/182378488
Key unmet needs in multiple sclerosis (MS) include detection of early pathology, disability worsening independent of relapses, and accurate monitoring of treatment response. Collaborative approaches to address these unmet needs have been driven in part by industry–academic networks and initiatives such as the Grant for Multiple Sclerosis Innovation (GMSI) and Multiple Sclerosis Leadership and Innovation Network (MS-LINK™) programs. We review the application of recent advances, supported by the GMSI and MS-LINK™ programs, in neuroimaging technology to quantify pathology related to central pathology and disease worsening, and potential for their translation into clinical practice/trials. GMSI-supported advances in neuroimaging methods and biomarkers include developments in magnetic resonance imaging, positron emission tomography, ocular imaging, and machine learning. However, longitudinal studies are required to facilitate translation of these measures to the clinic and to justify their inclusion as endpoints in clinical trials of new therapeutics for MS. Novel neuroimaging measures and other biomarkers, combined with artificial intelligence, may enable accurate prediction and monitoring of MS worsening in the clinic, and may also be used as endpoints in clinical trials of new therapies for MS targeting relapse-independent disease pathology.
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