Journal article
Clinical and therapeutic predictors of disease outcomes in AQP4-IgG neuromyelitis optica spectrum disorder
A Kunchok, C Malpas, P Nytrova, EK Havrdova, R Alroughani, M Terzi, B Yamout, JY Hor, R Karabudak, C Boz, S Ozakbas, J Olascoaga, M Simo, F Granella, F Patti, P McCombe, T Csepany, B Singhal, R Bergamaschi, Y Fragoso Show all
Multiple Sclerosis and Related Disorders | ELSEVIER SCI LTD | Published : 2020
Abstract
Background: Aquaporin-4-IgG positive (AQP4-IgG+) Neuromyelitis Optica Spectrum Disorder (NMOSD) is an uncommon central nervous system autoimmune disorder. Disease outcomes in AQP4-IgG+NMOSD are typically measured by relapse rate and disability. Using the MSBase, a multi-centre international registry, we aimed to examine the impact immunosuppressive therapies and patient characteristics as predictors of disease outcome measures in AQP4-IgG+NMOSD. Method: This MSBase cohort study of AQP4-IgG+NMOSD patients examined modifiers of relapse in a multivariable proportional hazards model and expanded disability status score (EDSS) using a mixed effects model. Results: 206 AQP4-IgG+ patients were incl..
View full abstractRelated Projects (3)
Grants
Awarded by International Parkinson and Movement Disorder Society
Funding Acknowledgements
This study was financially supported by National Health and Medical Research Council of Australia [project grants 1083539 and 1129189, and fellowships 1140766 and 1080518]. The MSBase Foundation is a not-for-profit organization that receives support from Merck, Biogen, Novartis, Bayer-Schering, Sanofi-Genzyme and Teva. The study was conducted separately and apart from the guidance of the sponsors.