Diagnosis of multiple sclerosis: 2024 revisions of the McDonald criteria

Xavier Montalban, Christine Lebrun-Frénay, Jiwon Oh, Georgina Arrambide, Marcello Moccia, Maria Pia Amato, Lilyana Amezcua, Brenda Banwell, Amit Bar-Or, Frederik Barkhof, Helmut Butzkueven, Olga Ciccarelli, Jeremy Chataway, Jeffrey A Cohen, Giancarlo Comi, Jorge Correale, Florian Deisenhammer, Massimo Filippi, Julie Fiol, Mark S Freedman, Alan J Thompson
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Abstract

Advances in the understanding of multiple sclerosis and the development of biomarkers of pathophysiology prompted a substantial revision of the 2017 McDonald diagnostic criteria. The new 2024 McDonald criteria provide a unified approach for diagnosing multiple sclerosis in individuals with relapsing or progressive courses throughout the lifespan (ie, from paediatric to late-life presentations). The optic nerve can now serve as a fifth anatomical location within the CNS for diagnosis. The central vein sign, paramagnetic rim lesions, and kappa free-light chain concentrations in CSF can be used, when available, to provide supportive evidence and confer specificity for a diagnosis of multiple sclerosis in specific situations. In certain cases, radiologically isolated syndrome or neurological symptoms that do not constitute a clear attack or progression of disability can fulfil the criteria for a multiple sclerosis diagnosis. We also provide guidance for the diagnosis of multiple sclerosis in older individuals (≥50 years) and those with comorbidities. The 2024 revised criteria should expedite the diagnosis of multiple sclerosis, while maintaining specificity.
多发性硬化症的诊断:麦当劳标准的2024修订版
对多发性硬化症认识的进步和病理生理学生物标志物的发展促使2017年麦当劳诊断标准进行了实质性修订。新的2024年麦当劳标准提供了一个统一的方法来诊断多发性硬化症患者在整个生命周期(即从儿科到晚年)的复发或进展过程。视神经现在可以作为中枢神经系统内的第五个解剖位置进行诊断。中央静脉征象、顺磁边缘病变和脑脊液kappa游离轻链浓度可用于提供支持性证据,并在特定情况下为多发性硬化症的诊断赋予特异性。在某些情况下,放射学上孤立的综合征或神经系统症状,不构成明显的发作或残疾的进展,可以满足多发性硬化症的诊断标准。我们还为老年人(≥50岁)和有合并症的多发性硬化症的诊断提供指导。2024年修订后的标准应加快多发性硬化症的诊断,同时保持特异性。
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