Hide metadata

dc.date.accessioned2020-11-24T20:04:08Z
dc.date.available2020-11-24T20:04:08Z
dc.date.created2020-11-05T15:01:55Z
dc.date.issued2020
dc.identifier.citationSimonsen, Cecilia Smith Flemmen, Heidi Øyen Broch, Line Brunborg, Cathrine Berg-Hansen, Pål Moen, Stine Marit Celius, Elisabeth Gulowsen . The course of multiple sclerosis rewritten: a Norwegian population-based study on disease demographics and progression. Neurology. 2020
dc.identifier.urihttp://hdl.handle.net/10852/81163
dc.description.abstractObjectives: Over the past few decades, there has been an improvement in the rate of disability progression in multiple sclerosis (MS) patients, and most studies relate this evolvement to the introduction of disease-modifying therapies. However, several other factors have changed over this period, including access to MRI and newer diagnostic criteria. The aim of this study is to investigate changes in the natural course of MS over time in a near-complete and geographically well-defined population from the south-east of Norway. Methods: We examined disease progression and demographics over two decades and assessed the effect of disease-modifying therapies using linear mixed-effect models. Results: In a cohort of 2097 patients, we found a significant improvement in disability as measured by the Expanded Disability Status Scale (EDSS) stratified by age, and the improvement remained significant after adjusting for time on disease-modifying medications, gender and progressive MS at onset. The time from disease onset to EDSS 6 in the total cohort was 29.8 years (95% CI 28.5-31.1) and was significantly longer in patients diagnosed after 2006 compared to patients diagnosed before. There are significant differences between patient demographics, as well as time to EDSS 6, in the near-complete, geographically well-defined population compared to an additional cohort from the capital Oslo and its suburbs. Conclusion: The natural course of MS is improving, but the improvement seen in disease progression has multifaceted explanations. Our study underlines the importance of completeness of data, relevant timeframes and demographics when comparing different MS populations. Studies on incomplete populations should be interpreted with caution.
dc.description.abstractThe course of multiple sclerosis rewritten: a Norwegian population-based study on disease demographics and progression
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleThe course of multiple sclerosis rewritten: a Norwegian population-based study on disease demographics and progression
dc.typeJournal article
dc.creator.authorSimonsen, Cecilia Smith
dc.creator.authorFlemmen, Heidi Øyen
dc.creator.authorBroch, Line
dc.creator.authorBrunborg, Cathrine
dc.creator.authorBerg-Hansen, Pål
dc.creator.authorMoen, Stine Marit
dc.creator.authorCelius, Elisabeth Gulowsen
cristin.unitcode185,53,42,13
cristin.unitnameNevrologisk avdeling
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin1845345
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Neurology&rft.volume=&rft.spage=&rft.date=2020
dc.identifier.jtitleNeurology
dc.identifier.pagecount12
dc.identifier.doihttps://doi.org/10.1007/s00415-020-10279-7
dc.identifier.urnURN:NBN:no-84244
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn0028-3878
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/81163/2/The%2Bcourse%2Bof%2Bmultiple%2Bsclerosis%2Brewritten_a%2BNorwegian.pdf
dc.type.versionPublishedVersion


Files in this item

Appears in the following Collection

Hide metadata

Attribution 4.0 International
This item's license is: Attribution 4.0 International