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Clinical and therapeutic predictors of disease outcomes in AQP4-IgG+ neuromyelitis optica spectrum disorder

Authors :
Kunchok, Amy
Malpas, Charles
Nytrova, Petra
Havrdova, Eva Kubala
Alroughani, Raed
Terzi, Murat
Yamout, Bassem
Hor, Jyh Yung
Karabudak, Rana
Boz, Cavit
Ozakbas, Serkan
Olascoaga, Javier
Simo, Magdolna
Granella, Franco
Patti, Francesco
McCombe, Pamela
Csepany, Tunde
Singhal, Bhim
Bergamaschi, Roberto
Fragoso, Yara
Al-Harbi, Talal
Turkoglu, Recai
Lechner-Scott, Jeannette
Laureys, Guy
Oreja-Guevara, Celia
Pucci, Eugenio
Sola, Patrizia
Ferraro, Diana
Altintas, Ayse
Soysal, Aysun
Vucic, Steve
Grand'Maison, Francois
Izquierdo, Guillermo
Eichau, Sara
Lugaresi, Alessandra
Onofrj, Marco
Trojano, Maria
Marriott, Mark
Butzkueven, Helmut
Kister, Ilya
Kalincik, Tomas
Source :
Multiple Sclerosis and Related Disorders; February 2020, Vol. 38 Issue: 1
Publication Year :
2020

Abstract

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.

Details

Language :
English
ISSN :
22110348
Volume :
38
Issue :
1
Database :
Supplemental Index
Journal :
Multiple Sclerosis and Related Disorders
Publication Type :
Periodical
Accession number :
ejs51850900
Full Text :
https://doi.org/10.1016/j.msard.2019.101868