| REVIEW ARTICLE |
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| Year : 2018 | Volume
: 30
| Issue : 4 | Page : 204-208 |
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Treatment strategies for neuromyelitis optica
Tzu-Lun Huang1, Kung-Hung Lin2, Jia-Kang Wang1, Rong-Kung Tsai3
1 Department of Ophthalmology, Far Eastern Memorial Hospital, New Taipei; Department of Electrical Engineering, Yuan Ze University, Taoyuan, Taiwan
2 Department of Neurology, Taiwan Adventist Hospital, Taipei, Taiwan
3 Institute of Medical Sciences, Tzu Chi University; Institute of Eye Research, Buddhist Tzu Chi General Hospital, Hualien, Taiwan
Correspondence Address:
Dr. Rong-Kung Tsai
Institute of Eye Research, Buddhist Tzu Chi General Hospital, 707, Section 3, Chung-Yang Road, Hualien
Taiwan
 Source of Support: None, Conflict of Interest: None  | 2 |
DOI: 10.4103/tcmj.tcmj_102_18
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Neuromyelitis optica (NMO) is an autoimmune demyelinating disease with pathogenic autoantibodies that act against the astrocyte water channel protein, i.e. aquaporin-4: the disease is associated with recurrent episodes of optic neuritis (ON) and transverse myelitis, often resulting in severe disability. The main goals in treatment of NMO include acute symptomatic therapy and long-term stabilization of symptoms by preventing relapse. In recent years, ongoing randomized controlled trials in NMO patients have studied evidence for treatment. Briefly, acute-stage management (with pulse therapy using corticosteroids and/or plasmapheresis) and maintenance therapy (including rituximab, mycophenolate mofetil, and azathioprine) have been recommended in some case series and retrospective studies. Because of the high prevalence of liver disease, all NMO patients in Taiwan should be screened for hepatitis B and C before treatment is initiated. Although immunosuppression and plasma exchange are the mainstays of therapy for NMO ON, several selective and potentially therapeutic strategies targeting specific steps in NMO pathogenesis including blockers of NMO-IgG binding and inhibitors of granulocyte function have been evaluated in recent years.
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