Diagnosis and treatment of anti-myelin oligodendrocyte glycoprotein antibody positive optic neuritis

被引:39
作者
Kezuka, Takeshi [1 ,2 ]
Ishikawa, Hitoshi [3 ]
机构
[1] KEZUKA Eye Clin, Sumida Ku, 1-5-7 Mukojima, Tokyo 1310033, Japan
[2] Tokyo Med Univ, Dept Ophthalmol, Tokyo, Japan
[3] Kitasato Univ, Sch Allied Hlth Sci, Dept Orthopt & Visual Sci, Sagamihara, Kanagawa, Japan
关键词
Anti-myelin oligodendrocyte glycoprotein antibody; Anti-MOG antibody; Optic neuritis; Chronic recurrent inflammatory optic neuropathy; NMO SPECTRUM DISORDERS; NEUROMYELITIS-OPTICA; MOG ANTIBODY; TREATMENT TRIAL; MULTICENTER; ENCEPHALOMYELITIS; AUTOANTIBODY; DISTINCTION; FEATURES; MOUSE;
D O I
10.1007/s10384-018-0561-1
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Anti-myelin-oligodendrocyte glycoprotein (MOG) antibody positive optic neuritis has been established as a new subset of optic neuropathy. Anti-MOG antibodies are usually measured by cell-based assay. Patients with anti-MOG antibody positive optic neuritis respond well to steroid therapy, and, while visual acuity outcomes are favorable, significant visual field defects remain. Furthermore, patients who are anti-MOG antibody positive have higher rates of recurrence compared to antibody negative patients. Based on these findings, anti-MOG antibody positive patients with optic neuritis have the characteristics of good visual outcomes, residual visual field defects, and high risk of recurrence. Tests for anti-MOG antibody are useful for the diagnosis and treatment of optic neuritis.
引用
收藏
页码:101 / 108
页数:8
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