Relapse activity in the chronic phase of anti-myelin-oligodendrocyte glycoprotein antibody-associated disease.

Anti-myelin oligodendrocyte glycoprotein (MOG) antibody MOG-antibody-associated disease (MOGAD) Neuromyelitis optica spectrum disorder (NMOSD) Relapse prevention Relapse-free survival

Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
Jun 2022
Historique:
received: 28 10 2021
accepted: 19 11 2021
revised: 19 11 2021
pubmed: 26 11 2021
medline: 24 5 2022
entrez: 25 11 2021
Statut: ppublish

Résumé

The patterns of relapse and relapse-prevention strategies for anti-myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) are not completely investigated. We compared the patterns of relapse in later stages of MOGAD with those of anti-aquaporin-4 antibody (AQP4-Ab)-positive neuromyelitis optica spectrum disorder (NMOSD). In this observational, comparative cohort study, 66 patients with MOGAD and 90 with AQP4-Ab-positive NMOSD were enrolled. We compared the patterns of relapse and annualized relapse rates (ARRs) in the first 10 years from disease onset, stratified by relapse-prevention treatments. Approximately 50% of the patients with MOGAD experienced relapses in the first 10 years. Among those not undergoing relapse-prevention treatments, ARRs in the first 5 years were slightly lower in MOGAD patients than in AQP4-Ab-positive NMOSD patients (MOGAD vs. AQP4-Ab NMOSD: 0.19 vs. 0.30; p = 0.0753). After 5 years, the ARR decreased in MOGAD patients (MOGAD vs. AQP4-Ab NMOSD: 0.05 vs. 0.34; p = 0.0001), with a 72% reduction from the first 5 years (p = 0.0090). Eight (61.5%) of the 13 MOGAD patients with more than 10-year follow-up from disease onset showed relapse 10 years after onset. Clustering in the timing and phenotype of attacks was observed in both disease patients. The effectiveness of long-term low-dose oral PSL for relapse prevention in patients with MOGAD has not been determined. The relapse risk in patients with MOGAD is generally lower than that in patients with AQP4-Ab-positive NMOSD, especially 5 years after onset. Meanwhile, relapses later than 10 years from onset are not rare in both diseases.

Identifiants

pubmed: 34820735
doi: 10.1007/s00415-021-10914-x
pii: 10.1007/s00415-021-10914-x
pmc: PMC9120114
doi:

Substances chimiques

Aquaporin 4 0
Autoantibodies 0
Myelin-Oligodendrocyte Glycoprotein 0
anti-aquaporin 4 autoantibody 0

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

3136-3146

Subventions

Organisme : Arthritis Research UK
ID : FC001030
Pays : United Kingdom
Organisme : Ministry of Health, Labour and Welfare
ID : 20FC1030
Organisme : Japan Society for the Promotion of Science London
ID : 20K07892

Informations de copyright

© 2021. The Author(s).

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Auteurs

Tetsuya Akaishi (T)

Department of Neurology, Tohoku University Graduate School of Medicine, Seiryo-machi 1-1, Aoba-ku, Sendai, Miyagi, 980-8574, Japan. t-akaishi@med.tohoku.ac.jp.
Department of Education and Support for Regional Medicine, Tohoku University Hospital, Sendai, Japan. t-akaishi@med.tohoku.ac.jp.

Tatsuro Misu (T)

Department of Neurology, Tohoku University Graduate School of Medicine, Seiryo-machi 1-1, Aoba-ku, Sendai, Miyagi, 980-8574, Japan.

Kazuo Fujihara (K)

Department of Neurology, Tohoku University Graduate School of Medicine, Seiryo-machi 1-1, Aoba-ku, Sendai, Miyagi, 980-8574, Japan.
Department of Multiple Sclerosis Therapeutics, Fukushima Medical University, Fukushima, Japan.

Toshiyuki Takahashi (T)

Department of Neurology, Tohoku University Graduate School of Medicine, Seiryo-machi 1-1, Aoba-ku, Sendai, Miyagi, 980-8574, Japan.
Department of Neurology, National Hospital Organization Yonezawa National Hospital, Yonezawa, Japan.

Yoshiki Takai (Y)

Department of Neurology, Tohoku University Graduate School of Medicine, Seiryo-machi 1-1, Aoba-ku, Sendai, Miyagi, 980-8574, Japan.

Shuhei Nishiyama (S)

Department of Neurology, Tohoku University Graduate School of Medicine, Seiryo-machi 1-1, Aoba-ku, Sendai, Miyagi, 980-8574, Japan.

Kimihiko Kaneko (K)

Department of Neurology, Tohoku University Graduate School of Medicine, Seiryo-machi 1-1, Aoba-ku, Sendai, Miyagi, 980-8574, Japan.

Juichi Fujimori (J)

Department of Neurology, Tohoku Medical and Pharmaceutical University, Sendai, Japan.

Tadashi Ishii (T)

Department of Education and Support for Regional Medicine, Tohoku University Hospital, Sendai, Japan.

Masashi Aoki (M)

Department of Neurology, Tohoku University Graduate School of Medicine, Seiryo-machi 1-1, Aoba-ku, Sendai, Miyagi, 980-8574, Japan.

Ichiro Nakashima (I)

Department of Neurology, Tohoku Medical and Pharmaceutical University, Sendai, Japan.

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