Replication of the 2023 radiologically isolated syndrome criteria in a multi-centre cohort.

IF 4.5 Q1 CLINICAL NEUROLOGY
Brain communications Pub Date : 2025-08-28 eCollection Date: 2025-01-01 DOI:10.1093/braincomms/fcaf323
Friederike Held, Paula Uibel, Cornelius Berberich, Jonas Schaller-Nagengast, Vasil Mitrevski, Leo Hutter, Hayrettin Tumani, Joachim Havla, Christiane Gasperi, Mark Mühlau, Achim Berthele, Jan S Kirschke, Bernhard Hemmer
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引用次数: 0

Abstract

Radiologically isolated syndrome (RIS) represents a pivotal stage for identifying individuals at high risk of transitioning into multiple sclerosis (MS). Early therapy initiation reduces the risk of conversion. The 2023-RIS criteria were proposed to identify presymptomatic individuals earlier. We aimed to replicate the diagnostic value of the 2023-RIS criteria in an independent cohort. In this retrospective cohort study, individuals diagnosed with RIS and longitudinally followed in three centres were stratified by the 2009- and 2023-RIS criteria. We conducted comparative analyses, including survival, hazard ratio and performance evaluations. Among n = 136 individuals, 27.2% converted to MS between 2009 and 2024 (observation time 55.4 months). We confirmed improved identification of individuals at risk using the 2023-RIS criteria (HR 4.30, P < 0.05; HR 4.71, P < 0.05) compared to 2009-RIS criteria (HR 1.32, P = 0.4; HR 1.43; P = 0.3) in 5- and 10-year intervals, respectively. 2023-RIS criteria demonstrated high sensitivity (94%) and negative predictive value (94%) but low specificity (29%). Adding CSF immunoglobulin G and M indices as an additional parameter following RIS diagnosis enhanced risk prediction specificity. We confirm the high sensitivity and predictive value of the 2023-RIS criteria for identifying individuals at risk of conversion to MS and suggest adding immunoglobulin indices to further improve specificity.

Abstract Image

Abstract Image

Abstract Image

2023放射隔离综合征标准在多中心队列中的复制
放射孤立综合征(RIS)是识别高风险过渡到多发性硬化症(MS)个体的关键阶段。早期开始治疗可降低转化的风险。2023-RIS标准被提出用于早期识别症状前个体。我们的目标是在一个独立的队列中重复2023-RIS标准的诊断价值。在这项回顾性队列研究中,诊断为RIS并在三个中心进行纵向随访的个体按照2009-和2023-RIS标准进行分层。我们进行了比较分析,包括生存率、风险比和绩效评估。2009 - 2024年间(观察时间55.4个月),136例患者中有27.2%转化为多发性硬化症。我们证实,与2009-RIS标准(HR 1.32, P = 0.4; HR 1.43, P = 0.3)相比,使用2023-RIS标准(HR 4.30, P < 0.05; HR 4.71, P < 0.05)在5年和10年的间隔时间内对高危个体的识别有所改善。2023-RIS标准具有高敏感性(94%)和阴性预测值(94%),但特异性较低(29%)。在RIS诊断后增加CSF免疫球蛋白G和M指数作为附加参数,可提高风险预测的特异性。我们确认2023-RIS标准在识别有转化为MS风险的个体方面具有很高的敏感性和预测价值,并建议增加免疫球蛋白指数以进一步提高特异性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
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6 weeks
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