Multiple Sclerosis and Neuroimmunology Program, Parkinson's and Movement Disorders Center, University Hospitals of Cleveland, Case Western Reserve University, Bolwell, 5th floor, 11100 Euclid Avenue, Cleveland, OH, 44106, USA.
Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
J Neurol. 2022 Apr;269(4):1786-1801. doi: 10.1007/s00415-021-10783-4. Epub 2021 Sep 5.
Neuromyelitis optica spectrum disorders (NMOSD) are a group of autoimmune inflammatory conditions that primarily target the optic nerves, spinal cord, brainstem, and occasionally the cerebrum. NMOSD is characterized by recurrent attacks of visual, motor, and/or sensory dysfunction that often result in severe neurological deficits. In recent years, there has been a significant progress in relapse treatment and prevention but the residual disability per attack remains high. Although symptomatic and restorative research has been limited in NMOSD, some therapeutic approaches can be inferred from published case series and evidence from multiple sclerosis literature. In this review, we will discuss established and emerging therapeutic options for symptomatic treatment and restoration of function in NMOSD. We highlight NMOSD-specific considerations and identify potential areas for future research. The review covers pharmacologic, non-pharmacologic, and neuromodulatory approaches to neuropathic pain, tonic spasms, muscle tone abnormalities, sphincter dysfunction, motor and visual impairment, fatigue, sleep disorders, and neuropsychological symptoms. In addition, we briefly discuss remyelinating agents and mesenchymal stem cell transplantation in NMOSD.
视神经脊髓炎谱系疾病(NMOSD)是一组主要靶向视神经、脊髓、脑干、偶尔也靶向大脑的自身免疫性炎症性疾病。NMOSD 的特征是反复发作的视觉、运动和/或感觉功能障碍,常导致严重的神经功能缺损。近年来,复发治疗和预防方面取得了显著进展,但每次发作后的残留残疾仍然很高。尽管 NMOSD 的症状性和恢复性研究有限,但从已发表的病例系列和多发性硬化症文献中的证据可以推断出一些治疗方法。在这篇综述中,我们将讨论 NMOSD 的症状性治疗和功能恢复的既定和新兴治疗选择。我们强调了 NMOSD 的特异性考虑因素,并确定了未来研究的潜在领域。该综述涵盖了神经病理性疼痛、强直性痉挛、肌肉张力异常、括约肌功能障碍、运动和视力障碍、疲劳、睡眠障碍和神经心理学症状的药物和非药物以及神经调节方法。此外,我们还简要讨论了 NMOSD 中的髓鞘修复剂和间充质干细胞移植。