脑脊液无kappa轻链预测早期多发性硬化症活动。

IF 7.5
Klaus Berek, Gabriel Bsteh, Michael Auer, Franziska Di Pauli, Astrid Grams, Dejan Milosavljevic, Paulina Poskaite, Christine Schnabl, Sebastian Wurth, Anne Zinganell, Thomas Berger, Janette Walde, Florian Deisenhammer, Harald Hegen
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引用次数: 23

摘要

目的:探讨κ游离轻链(κ-FLC)指数能否独立于人口统计学、临床特征和MRI表现预测多发性硬化症(MS)的疾病活动性。方法:对发病时进行脑脊液和血清取样的早期MS患者进行4年随访。在基线时,确定年龄、性别、症状类型、皮质类固醇治疗以及MRI上T2高信号(T2L)和增强T1病变(CELs)的数量。在随访期间,记录第二次临床发作的发生和疾病改善治疗(DMT)的开始。用比浊法测定κ-FLC,计算κ-FLC指数为[CSF κ-FLC/血清κ-FLC]/白蛋白商。结果:共纳入88例患者,平均年龄33±10岁,女性占68%;38例(43%)患者在随访期间出现第二次临床发作。在调整年龄、性别、T2L、CEL、疾病和随访时间的多因素Cox回归分析中,基线时皮质激素给药和随访期间DMT显示κ-FLC指数预测第二次临床发作时间。基线时κ-FLC指数>100(中位值147)的患者在12个月内第二次临床发作的概率是κ-FLC指数低(中位值28)患者的两倍;在24个月内,高κ-FLC指数患者的发病几率是低κ-FLC指数患者的4倍。高κ-FLC指数组至第二次发作的中位时间为11个月,低κ-FLC指数组为36个月。结论:高κ-FLC指数可预测MS疾病早期活动性。证据分类:本研究提供ⅱ类证据,在早期MS患者中,高κ-FLC指数是早期第二次临床发作的独立危险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Kappa-Free Light Chains in CSF Predict Early Multiple Sclerosis Disease Activity.

Kappa-Free Light Chains in CSF Predict Early Multiple Sclerosis Disease Activity.

Kappa-Free Light Chains in CSF Predict Early Multiple Sclerosis Disease Activity.

Kappa-Free Light Chains in CSF Predict Early Multiple Sclerosis Disease Activity.

Objective: To investigate whether κ-free light chain (κ-FLC) index predicts multiple sclerosis (MS) disease activity independent of demographics, clinical characteristics, and MRI findings.

Methods: Patients with early MS who had CSF and serum sampling at disease onset were followed for 4 years. At baseline, age, sex, type of symptoms, corticosteroid treatment, and number of T2 hyperintense (T2L) and contrast-enhancing T1 lesions (CELs) on MRI were determined. During follow-up, the occurrence of a second clinical attack and start of disease-modifying therapy (DMT) were registered. κ-FLCs were measured by nephelometry, and κ-FLC index calculated as [CSF κ-FLC/serum κ-FLC]/albumin quotient.

Results: A total of 88 patients at a mean age of 33 ± 10 years and female predominance of 68% were included; 38 (43%) patients experienced a second clinical attack during follow-up. In multivariate Cox regression analysis adjusting for age, sex, T2L, CEL, disease and follow-up duration, administration of corticosteroids at baseline and DMT during follow-up revealed that κ-FLC index predicts time to second clinical attack. Patients with κ-FLC index >100 (median value 147) at baseline had a twice as high probability for a second clinical attack within 12 months than patients with low κ-FLC index (median 28); within 24 months, the chance in patients with high κ-FLC index was 4 times as high as in patients with low κ-FLC index. The median time to second attack was 11 months in patients with high κ-FLC index whereas 36 months in those with low κ-FLC index.

Conclusion: High κ-FLC index predicts early MS disease activity.

Classification of evidence: This study provides Class II evidence that in patients with early MS, high κ-FLC index is an independent risk factor for early second clinical attack.

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