医学
视神经脊髓炎
光谱紊乱
髓鞘少突胶质细胞糖蛋白
多发性硬化
皮肤病科
视神经炎
疾病
病理
免疫学
精神科
实验性自身免疫性脑脊髓炎
作者
Laura Cacciaguerra,Eoin P. Flanagan
标识
DOI:10.1016/j.ncl.2023.06.009
摘要
Aquaporin-4-IgG positive neuromyelitis optica spectrum disorder (AQP4+NMOSD) and myelin-oligodendrocyte glycoprotein antibody-associated disease (MOGAD) are antibody-associated diseases targeting astrocytes and oligodendrocytes, respectively. Their recognition as distinct entities has led to each having its own diagnostic criteria that require a combination of clinical, serologic, and MRI features. The therapeutic approach to acute attacks in AQP4+NMOSD and MOGAD is similar. There is now class 1 evidence to support attack-prevention medications for AQP4+NMOSD. MOGAD lacks proven treatments although clinical trials are now underway. In this review, we will outline similarities and differences between AQP4+NMOSD and MOGAD in terms of diagnosis and treatment.
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