Rodin Rachel E, Chitnis Tanuja
Department of Neurology, Brigham MS Center, Brigham and Women's Hospital, Boston, MA, United States.
Harvard Medical School, Boston, MA, United States.
Front Neurol. 2024 May 16;15:1415535. doi: 10.3389/fneur.2024.1415535. eCollection 2024.
The Neuromyelitis Optica Spectrum Disorders (NMOSD) constitute a spectrum of rare autoimmune diseases of the central nervous system characterized by episodes of transverse myelitis, optic neuritis, and other demyelinating attacks. Previously thought to be a subtype of multiple sclerosis, NMOSD is now known to be a distinct disease with unique pathophysiology, clinical course, and treatment options. Although there have been significant recent advances in the diagnosis and treatment of NMOSD, the field still lacks clinically validated biomarkers that can be used to stratify disease severity, monitor disease activity, and inform treatment decisions. Here we review many emerging NMOSD biomarkers including markers of cellular damage, neutrophil-to-lymphocyte ratio, complement, and cytokines, with a focus on how each biomarker can potentially be used for initial diagnosis, relapse surveillance, disability prediction, and treatment monitoring.
视神经脊髓炎谱系障碍(NMOSD)是一组罕见的中枢神经系统自身免疫性疾病,其特征为横贯性脊髓炎、视神经炎和其他脱髓鞘发作。NMOSD以前被认为是多发性硬化症的一种亚型,现在已知是一种具有独特病理生理学、临床病程和治疗选择的独特疾病。尽管最近在NMOSD的诊断和治疗方面取得了重大进展,但该领域仍然缺乏可用于对疾病严重程度进行分层、监测疾病活动并为治疗决策提供依据的经过临床验证的生物标志物。在此,我们综述了许多新兴的NMOSD生物标志物,包括细胞损伤标志物、中性粒细胞与淋巴细胞比率、补体和细胞因子,重点关注每种生物标志物如何潜在地用于初始诊断、复发监测、残疾预测和治疗监测。