Back to Search Start Over

Predicting clinical progression in multiple sclerosis after 6 and 12 years

Authors :
Iris Dekker
Lisanne J. Balk
Frederik Barkhof
Menno M. Schoonheim
B.M.J. Uitdehaag
Veronica Popescu
Jeroen J. G. Geurts
Anand J. C. Eijlers
Mike P. Wattjes
Joep Killestein
Hugo Vrenken
Radiology and nuclear medicine
Anatomy and neurosciences
VU University medical center
Neurology
Amsterdam Neuroscience - Neuroinfection & -inflammation
Other Research
AII - Inflammatory diseases
Source :
European Journal of Neurology, Dekker, I, Eijlers, A J C, Popescu, V, Balk, L J, Vrenken, H, Wattjes, M P, Uitdehaag, B M J, Killestein, J, Geurts, J J G, Barkhof, F & Schoonheim, M M 2019, ' Predicting clinical progression in multiple sclerosis after 6 and 12 years ', European Journal of Neurology, vol. 26, no. 6, pp. 893-902 . https://doi.org/10.1111/ene.13904, European Journal of Neurology, 26(6), 893-902. Wiley-Blackwell
Publication Year :
2019
Publisher :
John Wiley and Sons Inc., 2019.

Abstract

Background and purpose: To predict disability and cognition in multiple sclerosis (MS) after 6 and 12 years, using early clinical and imaging measures. Methods: A total of 115 patients with MS were selected and followed up after 2 and 6 years, with 79 patients also being followed up after 12 years. Disability was measured using the Expanded Disability Status Scale (EDSS); cognition was measured only at follow-up using neuropsychological testing. Predictors of interest included EDSS score, baseline brain and lesion volumes and their changes over 2 years, baseline age, clinical phenotype, sex and educational level. Results: Higher 6-year EDSS score was predicted by early EDSS score and whole-brain volume changes and baseline diagnosis of primary progressive MS (adjusted R 2 = 0.56). Predictors for 12-year EDSS score included larger EDSS score changes and higher T1-hypointense lesion volumes (adjusted R 2 = 0.38). Year 6 cognition was predicted by primary progressive MS phenotype, lower educational level, male sex and early whole-brain atrophy (adjusted R 2 = 0.26); year 12 predictors included male sex, lower educational level and higher baseline T1-hypointense lesion volumes (adjusted R 2 = 0.14). Conclusions: Patients with early signs of neurodegeneration and a progressive disease onset were more prone to develop both disability progression and cognitive dysfunction. Male sex and lower educational level only affected cognitive dysfunction, which remains difficult to predict and probably needs more advanced imaging measures.

Details

Language :
English
ISSN :
14681331 and 13515101
Volume :
26
Issue :
6
Database :
OpenAIRE
Journal :
European Journal of Neurology
Accession number :
edsair.doi.dedup.....705d2a8798677b82d0bd0002d5603aa0
Full Text :
https://doi.org/10.1111/ene.13904