| Literature DB >> 33781189 |
Yi Du1, Kaijun Li1, Wei Liu1, Ruitong Song1, Meifeng Luo1, Jianfeng He1, Xiaoyu Xu2, Xiaosheng Qu3.
Abstract
Neuromyelitis optica spectrum disorder (NMOSD) is an acute or subacute demyelinating disease that affects mainly the optic nerve and spinal cord. A major proportion of NMOSD cases have a relationship with autoimmunity to aquaporin 4 (AQP4) found on the central nervous system. NMOSD can occur repeatedly, causing symptoms such as decreased vision and weakness of limbs. The main goal of the current therapy is to relieve acute symptoms and prevent recurrence of the disease. Without timely and appropriate treatment, the recurrence and disability rates are high. In the present work, we review recent advances in the diagnosis and treatment of patients with NMOSD, as well as the pathogenesis and mechanisms of AQP4-IgG-seropositive NMOSD. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.Entities:
Keywords: AQP4; Devic’s disease; NMOSD; autoimmunity; pathogenesis; therapy
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Year: 2022 PMID: 33781189 DOI: 10.2174/1381612827666210329101335
Source DB: PubMed Journal: Curr Pharm Des ISSN: 1381-6128 Impact factor: 3.116