» Articles » PMID: 30893099

Neuromyelitis Optica Spectrum Disorders: Still Evolving and Broadening

Overview
Specialty Neurology
Date 2019 Mar 21
PMID 30893099
Citations 62
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose Of Review: The diagnostic criteria of neuromyelitis optica spectrum disorders (NMOSD) has been revised in the past 20 years and pathological and therapeutic data have been accumulated. This review provides an overview of evolution and broadening of the concept of NMOSD.

Recent Findings: NMOSD encompassing brain syndrome as well as optic neuritis and acute myelitis is now classified into aquaporine-4 (AQP)-antibody-seropositive and aquaporine-4 (AQP)-antibody-seronegative diseases, detecting more patients earlier than before. Seronegative NMOSD includes cases of myelin oligodendrocyte glycoprotein (MOG)-antibody-seropositive disease with its unique clinical spectrum somewhat different from AQP4-antibody-seropositive NMOSD. Pathologically, NMOSD includes AQP4-antibody-seropositive autoimmune astrocytopathic disease and MOG-antibody-seropositive inflammatory demyelinating disease. Double seronegative group needs further research. Therapeutic options of NMOSD has taken shape and first-ever clinical trials of monoclonal antibodies have been done. In retrospect, relapsing NMO in the studies preceding the discovery of AQP4-antibody had features of AQP4-antibody-seropositive NMO whereas monophasic NMO was similar to AQP4-antibody-seronegative/MOG-antibody-seropositive NMO.

Summary: The clinical, pathological and therapeutic concepts of NMOSD have evolved and broadened over the last two decades following the detection of AQP4 antibodies and MOG antibodies in the patients. Double seronegative NMOSD is a current research focus, but now we may need to reconsider how NMOSD should be defined.

Citing Articles

Serum Low-Density Lipoprotein Cholesterol Levels are Associated with Relapse in Neuromyelitis Optica Spectrum Disorder.

Ding J, Chen F, Song Y, Li H, Ai X, Chen Y J Inflamm Res. 2024; 17:8227-8240.

PMID: 39525310 PMC: 11549894. DOI: 10.2147/JIR.S489723.


Imaging Transcriptomics of Brain Functional Alterations in MS and Neuromyelitis Optica Spectrum Disorder.

Li Y, Sun J, Zhuo Z, Guo M, Duan Y, Xu X AJNR Am J Neuroradiol. 2024; 45(12):1901-1909.

PMID: 39510804 PMC: 11630882. DOI: 10.3174/ajnr.A8480.


Usage status of biologics for the chronic treatment of optic neuritis in neuromyelitis optica spectrum disorders in Japan.

Takahashi Y, Kezuka T, Shikishima K, Yamagami A, Chuman H, Nakamura M Jpn J Ophthalmol. 2024; 69(1):81-92.

PMID: 39470886 PMC: 11821680. DOI: 10.1007/s10384-024-01129-4.


Biomarkers for neuromyelitis optica: a visual analysis of emerging research trends.

Li X, Zhang J, Zhang S, Shi S, Lu Y, Leng Y Neural Regen Res. 2024; 19(12):2735-2749.

PMID: 38595291 PMC: 11168523. DOI: 10.4103/NRR.NRR-D-24-00109.


Advances in the long-term treatment of neuromyelitis optica spectrum disorder.

Anderson M, Levy M J Cent Nerv Syst Dis. 2024; 16:11795735241231094.

PMID: 38312734 PMC: 10836138. DOI: 10.1177/11795735241231094.


References
1.
Hamid S, Elsone L, Mutch K, Solomon T, Jacob A . The impact of 2015 neuromyelitis optica spectrum disorders criteria on diagnostic rates. Mult Scler. 2016; 23(2):228-233. DOI: 10.1177/1352458516663853. View

2.
Waters P, Woodhall M, OConnor K, Reindl M, Lang B, Sato D . MOG cell-based assay detects non-MS patients with inflammatory neurologic disease. Neurol Neuroimmunol Neuroinflamm. 2015; 2(3):e89. PMC: 4370386. DOI: 10.1212/NXI.0000000000000089. View

3.
Roemer S, Parisi J, Lennon V, Benarroch E, Lassmann H, Bruck W . Pattern-specific loss of aquaporin-4 immunoreactivity distinguishes neuromyelitis optica from multiple sclerosis. Brain. 2007; 130(Pt 5):1194-205. DOI: 10.1093/brain/awl371. View

4.
Jurynczyk M, Jacob A, Fujihara K, Palace J . Myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease: practical considerations. Pract Neurol. 2018; 19(3):187-195. DOI: 10.1136/practneurol-2017-001787. View

5.
Kitley J, Waters P, Woodhall M, Leite M, Murchison A, George J . Neuromyelitis optica spectrum disorders with aquaporin-4 and myelin-oligodendrocyte glycoprotein antibodies: a comparative study. JAMA Neurol. 2014; 71(3):276-83. DOI: 10.1001/jamaneurol.2013.5857. View