<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>145(9)</volume><submitter>Lublin FD</submitter><funding>Novartis Pharma AG</funding><pubmed_abstract>Patients with multiple sclerosis acquire disability either through relapse-associated worsening (RAW) or progression independent of relapse activity (PIRA). This study addresses the relative contribution of relapses to disability worsening over the course of the disease, how early progression begins and the extent to which multiple sclerosis therapies delay disability accumulation. Using the Novartis-Oxford multiple sclerosis (NO.MS) data pool spanning all multiple sclerosis phenotypes and paediatric multiple sclerosis, we evaluated ∼200 000 Expanded Disability Status Scale (EDSS) transitions from >27 000 patients with ≤15 years follow-up. We analysed three datasets: (i) A full analysis dataset containing all observational and randomized controlled clinical trials in which disability and r</pubmed_abstract><journal>Brain : a journal of neurology</journal><pagination>3147-3161</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9536294</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>How patients with multiple sclerosis acquire disability.</pubmed_title><pmcid>PMC9536294</pmcid><pubmed_authors>Ocampo A</pubmed_authors><pubmed_authors>Cuklina J</pubmed_authors><pubmed_authors>Wiendl H</pubmed_authors><pubmed_authors>Arnold DL</pubmed_authors><pubmed_authors>Lublin FD</pubmed_authors><pubmed_authors>Nichols TE</pubmed_authors><pubmed_authors>Hatami F</pubmed_authors><pubmed_authors>Kieseier BC</pubmed_authors><pubmed_authors>Bermel RA</pubmed_authors><pubmed_authors>Aarden P</pubmed_authors><pubmed_authors>Dahlke F</pubmed_authors><pubmed_authors>Ganjgahi H</pubmed_authors><pubmed_authors>Haring DA</pubmed_authors><pubmed_authors>Chitnis T</pubmed_authors></additional><is_claimable>false</is_claimable><name>How patients with multiple sclerosis acquire disability.</name><description>Patients with multiple sclerosis acquire disability either through relapse-associated worsening (RAW) or progression independent of relapse activity (PIRA). This study addresses the relative contribution of relapses to disability worsening over the course of the disease, how early progression begins and the extent to which multiple sclerosis therapies delay disability accumulation. Using the Novartis-Oxford multiple sclerosis (NO.MS) data pool spanning all multiple sclerosis phenotypes and paediatric multiple sclerosis, we evaluated ∼200 000 Expanded Disability Status Scale (EDSS) transitions from >27 000 patients with ≤15 years follow-up. We analysed three datasets: (i) A full analysis dataset containing all observational and randomized controlled clinical trials in which disability and r</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-18T21:00:53.144Z</modification><creation>2025-04-07T09:01:17.045Z</creation></dates><accession>S-EPMC9536294</accession><cross_references><pubmed>35104840</pubmed><doi>10.1093/brain/awac016</doi></cross_references></HashMap>