Diagnostic Utility of Kappa Free Light Chain Index in Adults With Inaugural Optic Neuritis.

IF 7.8 1区 医学 Q1 CLINICAL NEUROLOGY
Sarah Demortiere, Natacha Stolowy, Marine Perriguey, Clemence Boutiere, Audrey Rico, Frederic Hilezian, Blaise-Roger Ndjomo-Ndjomo, Pierre Durozard, Jan-Patrick Stellmann, Romain Marignier, José Boucraut, Jean Pelletier, Adil Maarouf, Bertrand Audoin
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引用次数: 0

Abstract

Background and objectives: A simple, quick, and reproducible procedure for distinguishing multiple sclerosis (MS), myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD), and neuromyelitis optica spectrum disorder (NMOSD) at inaugural optic neuritis (ION) could be highly valuable in guiding early management.

Methods: We included all adults admitted to the MS center of Marseille for ION between March 2016 and April 2024, with CSF analysis including the kappa free light chain (K-FLC) index. Receiver operating characteristic curves were used to measure the diagnostic ability of the K-FLC index.

Results: Two hundred twenty-seven adults were admitted for ION; 210 (93%) had a K-FLC index measurement. MS was diagnosed in 84 (40%); clinically isolated syndrome suggestive of MS in 77 (36.5%), including 20 with future conversion to MS (CISwc); MOGAD in 26 (12.5%); NMOSD in 13 (6%); and other inflammatory disorders in 10 (5%). A K-FLC index ≥6.7 differentiated MS/CISwc from other diagnoses with specificity 86% and sensitivity 95% (area under the curve [AUC] 0.94). A K-FLC index <4.9 differentiated MOGAD from other diagnoses with specificity 63% and sensitivity 92% (AUC 0.78) and MOGAD from MS/CISwc with specificity 96% and sensitivity 92% (AUC 0.97). Among all patients, 93 (44%) had a K-FLC index <4.9: 24 of these (26%) had MOGAD and 5 (5.5%) MS/CISwc. Among the remaining patients with a K-FLC index ≥4.9 (n = 117), 2 (1.7%) had MOGAD (K-FLC index of 7.9 and 16.2) and 99 (85%) MS/CISwc. Among patients with normal MRI (n = 96), 73 (76%) had a K-FLC index <4.9: 22 of these (30%) had MOGAD, and none showed conversion to MS. Among the remaining patients with a K-FLC index ≥4.9 (n = 23), 2 (8.5%) had MOGAD and 7 (30.5%) showed conversion to MS. The K-FLC index did not differentiate NMOSD from other diagnoses and only moderately differentiated NMO from MS/CISwc (AUC 0.80).

Discussion: The K-FLC index is an accessible biomarker to guide early diagnosis in patients with ION. The probability of MOGAD in patients with ION and a K-FLC index ≥4.9 is low even in case of normal brain/spinal cord MRI.

Classification of evidence: This study provides Class II evidence that for patients with ION, the K-FLC index can distinguish between MS/CISwc and MOGAD.

Kappa游离轻链指数在成人首发视神经炎中的诊断价值。
背景和目的:一种简单、快速、可重复的方法来区分多发性硬化症(MS)、髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)和视神经脊髓炎视谱障碍(NMOSD),对于指导视神经炎(ION)的早期治疗具有重要价值。方法:我们纳入了2016年3月至2024年4月期间在马赛MS中心接受ION治疗的所有成年人,并进行了CSF分析,包括kappa自由轻链(K-FLC)指数。采用受试者工作特征曲线衡量K-FLC指数的诊断能力。结果:有227名成人因ION入院;210例(93%)有K-FLC指数测定。84例(40%)被诊断为多发性硬化症;临床孤立综合征提示多发性硬化症77例(36.5%),其中20例未来转化为多发性硬化症(CISwc);MOGAD 26个(12.5%);NMOSD 13例(6%);其他炎症性疾病10例(5%)。K-FLC指数≥6.7区分MS/CISwc与其他诊断的特异性为86%,敏感性为95%(曲线下面积[AUC] 0.94)。讨论:K-FLC指数是一个可获得的生物标志物,可指导ION患者的早期诊断。即使在脑/脊髓MRI正常的情况下,K-FLC指数≥4.9的ION患者发生MOGAD的概率也很低。证据分类:本研究提供II类证据,对于ION患者,K-FLC指数可以区分MS/CISwc和MOGAD。
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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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