Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Department of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
J Neurol. 2022 Jun;269(6):2827-2839. doi: 10.1007/s00415-022-11050-w. Epub 2022 Mar 30.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the aetiologic agent of the coronavirus disease 2019 (COVID-19), is now rapidly disseminating throughout the world with 147,443,848 cases reported so far. Around 30-80% of cases (depending on COVID-19 severity) are reported to have neurological manifestations including anosmia, stroke, and encephalopathy. In addition, some patients have recognised autoimmune neurological disorders, including both central (limbic and brainstem encephalitis, acute disseminated encephalomyelitis [ADEM], and myelitis) and peripheral diseases (Guillain-Barré and Miller Fisher syndrome). We systematically describe data from 133 reported series on the Neurology and Neuropsychiatry of COVID-19 blog ( https://blogs.bmj.com/jnnp/2020/05/01/the-neurology-and-neuropsychiatry-of-covid-19/ ) providing a comprehensive overview concerning the diagnosis, and treatment of patients with neurological immune-mediated complications of SARS-CoV-2. In most cases the latency to neurological disorder was highly variable and the immunological or other mechanisms involved were unclear. Despite specific neuronal or ganglioside antibodies only being identified in 10, many had apparent responses to immunotherapies. Although the proportion of patients experiencing immune-mediated neurological disorders is small, the total number is likely to be underestimated. The early recognition and improvement seen with use of immunomodulatory treatment, even in those without identified autoantibodies, makes delayed or missed diagnoses risk the potential for long-term disability, including the emerging challenge of post-acute COVID-19 sequelae (PACS). Finally, potential issues regarding the use of immunotherapies in patients with pre-existent neuro-immunological disorders are also discussed.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)是 2019 年冠状病毒病(COVID-19)的病原体,目前正在全球迅速传播,迄今已报告 147443848 例病例。据报道,约 30-80%的病例(取决于 COVID-19 的严重程度)有神经系统表现,包括嗅觉丧失、中风和脑病。此外,一些患者出现了公认的自身免疫性神经系统疾病,包括中枢神经系统(边缘和脑干脑炎、急性播散性脑脊髓炎[ADEM]和脊髓炎)和周围神经系统疾病(吉兰-巴雷和米勒-费舍尔综合征)。我们系统地描述了来自 COVID-19 博客(https://blogs.bmj.com/jnnp/2020/05/01/the-neurology-and-neuropsychiatry-of-covid-19/)上的 133 份报告系列中的数据,提供了关于 SARS-CoV-2 引起的神经免疫介导并发症患者的诊断和治疗的综合概述。在大多数情况下,神经障碍的潜伏期高度可变,涉及的免疫或其他机制尚不清楚。尽管只有 10 例患者中明确识别出特定的神经元或神经节苷脂抗体,但许多患者对免疫疗法有明显反应。尽管经历免疫介导的神经系统疾病的患者比例很小,但总数可能被低估。即使在没有识别出自身抗体的患者中,使用免疫调节治疗也能早期识别和改善,延迟或漏诊会增加长期残疾的风险,包括新兴的 COVID-19 后后遗症(PACS)挑战。最后,还讨论了在存在神经免疫疾病的患者中使用免疫疗法的潜在问题。