From Diagnosis to Disease Staging: Multisite Validation of Cerebrospinal Fluid Molecular Tests in Multiple Sclerosis.

IF 7.7 1区 医学 Q1 CLINICAL NEUROLOGY
Laura Ghezzi, Peter Kosa, Mark Greenwood, Enrique Alvarez, C L Freedman, Anne H Cross, Francesca Pace, Mark S Freedman, Joanna Kocot, Laura Piccio, Bibiana Bielekova
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Abstract

Objective: The growing demand for personalized treatment in multiple sclerosis (MS) highlights the need for more precise biomarkers that can outperform magnetic resonance imaging and clinical assessment in patient stratification. Advances in multiplex proteomic technologies suggest that cerebrospinal fluid (CSF) analysis at MS onset may not only improve diagnostic accuracy, but also offer prognostic and staging information, as well as insight into molecular therapeutic targets.

Methods: This multicenter study retrospectively analyzed cryopreserved CSF samples from 160 individuals undergoing diagnostic evaluation for possible neuroimmunological disorder, and among these, followed a cohort of 96 people with confirmed MS for at least 3 years. The goal was to externally validate previously published CSF-based diagnostic and prognostic classifiers.

Results: Upon unblinding, the CSF-based molecular diagnostic test distinguished 96 people with confirmed MS from 30 individuals with other inflammatory neurological diseases, and 34 individuals with non-inflammatory neurological diseases, achieving an area under the receiver operating characteristic curve of 0.94 (p = 4.7 × 10-21). The test also differentiated 65 individuals with relapsing-remitting MS from 31 individuals with progressive MS, with an area under the receiver operating characteristic curve of 0.76 (p = 1.4 × 10-5). The prognostic classifier predicted prospectively measured Expanded Disability Status Scale scores at follow up (rho = 0.43, p = 2.54 × 10-5).

Interpretation: This multicenter external validation study demonstrates that CSF-based molecular tests can robustly distinguish MS from other neurological conditions, stratify MS subtypes, and predict future disability progression in real-world settings. These results lay the groundwork for development of next-generation molecular tools to personalize care in MS. ANN NEUROL 2025.

从诊断到疾病分期:多发性硬化症脑脊液分子检测的多位点验证。
目的:对多发性硬化症(MS)个性化治疗日益增长的需求凸显了对更精确的生物标志物的需求,这些生物标志物可以在患者分层中优于磁共振成像和临床评估。多重蛋白质组学技术的进步表明,在多发性硬化症发病时进行脑脊液(CSF)分析不仅可以提高诊断的准确性,还可以提供预后和分期信息,以及深入了解分子治疗靶点。方法:这项多中心研究回顾性分析了160名接受可能的神经免疫疾病诊断评估的个体冷冻保存的脑脊液样本,其中96名确诊为多发性硬化症的患者随访至少3年。目的是外部验证先前发表的基于csf的诊断和预后分类器。结果:解盲后,基于csf的分子诊断试验将96例MS确诊患者与30例其他炎性神经系统疾病患者和34例非炎性神经系统疾病患者区分开来,患者工作特征曲线下面积为0.94 (p = 4.7 × 10-21)。该试验还区分了65例复发缓解型多发性硬化患者和31例进展型多发性硬化患者,受试者工作特征曲线下面积为0.76 (p = 1.4 × 10-5)。预后分类器预测随访时测量的扩展残疾状态量表评分(rho = 0.43, p = 2.54 × 10-5)。解释:这项多中心外部验证研究表明,基于csf的分子测试可以有效地将MS与其他神经系统疾病区分开来,对MS亚型进行分层,并预测现实环境中未来的残疾进展。这些结果为MS. ANN NEUROL 2025中个性化护理的下一代分子工具的开发奠定了基础。
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来源期刊
Annals of Neurology
Annals of Neurology 医学-临床神经学
CiteScore
18.00
自引率
1.80%
发文量
270
审稿时长
3-8 weeks
期刊介绍: Annals of Neurology publishes original articles with potential for high impact in understanding the pathogenesis, clinical and laboratory features, diagnosis, treatment, outcomes and science underlying diseases of the human nervous system. Articles should ideally be of broad interest to the academic neurological community rather than solely to subspecialists in a particular field. Studies involving experimental model system, including those in cell and organ cultures and animals, of direct translational relevance to the understanding of neurological disease are also encouraged.
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