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定义活跃进展型多发性硬化症。

Defining active progressive multiple sclerosis.

机构信息

Danish Multiple Sclerosis Center, Department of Neurology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Neurogenetics Clinic, Danish Dementia Research Centre, Department of Neurology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

出版信息

Mult Scler. 2017 Nov;23(13):1727-1735. doi: 10.1177/1352458517726592. Epub 2017 Aug 23.

Abstract

BACKGROUND

It is unknown whether disease activity according to consensus criteria (magnetic resonance imaging activity or clinical relapses) associate with cerebrospinal fluid (CSF) changes in progressive multiple sclerosis (MS).

OBJECTIVE

To compare CSF biomarkers in active and inactive progressive MS according to consensus criteria.

METHODS

Neurofilament light chain (NFL), myelin basic protein (MBP), IgG-index, chitinase-3-like-1 (CHI3L1), matrix metalloproteinase-9 (MMP-9), chemokine CXCL13, terminal complement complex, leukocyte counts and nitric oxide metabolites were measured in primary ( n = 26) and secondary progressive MS ( n = 26) and healthy controls ( n = 24).

RESULTS

Progressive MS patients had higher CSF cell counts, IgG-index, CHI3L1, MMP-9, CXCL13, NFL and MBP concentrations. Active patients were younger and had higher NFL, CXCL13 and MMP-9 concentrations than inactive patients. Patients with active disease according to consensus criteria or detectable CXCL13 or MMP-9 in CSF were defined as having combined active progressive MS. These patients had increased CSF cell counts, IgG-index and MBP, NFL and CHI3L1 concentrations. Combined inactive patients only had increased IgG-index and MBP concentrations.

CONCLUSION

Patients with combined active progressive MS show evidence of inflammation, demyelination and neuronal/axonal damage, whereas the remaining patients mainly show evidence of active demyelination. This challenges the idea that neurodegeneration independent of inflammation is crucial in disease progression.

摘要

背景

根据共识标准(磁共振成像活动或临床复发)确定的疾病活动是否与进展性多发性硬化症(MS)中的脑脊液(CSF)变化相关尚不清楚。

目的

根据共识标准比较活跃和不活跃的进展性 MS 中的 CSF 生物标志物。

方法

在原发性 MS(n = 26)和继发性进展性 MS(n = 26)和健康对照组(n = 24)中测量神经丝轻链(NFL)、髓鞘碱性蛋白(MBP)、IgG 指数、几丁质酶 3 样蛋白 1(CHI3L1)、基质金属蛋白酶 9(MMP-9)、趋化因子 CXCL13、末端补体复合物、白细胞计数和一氧化氮代谢物。

结果

进展性 MS 患者的 CSF 细胞计数、IgG 指数、CHI3L1、MMP-9、CXCL13、NFL 和 MBP 浓度更高。活跃患者比不活跃患者更年轻,且 NFL、CXCL13 和 MMP-9 浓度更高。根据共识标准确定的活跃患者或可检测到 CSF 中的 CXCL13 或 MMP-9 的患者被定义为合并活跃进展性 MS。这些患者的 CSF 细胞计数、IgG 指数和 MBP、NFL 和 CHI3L1 浓度增加。合并的不活跃患者仅 IgG 指数和 MBP 浓度增加。

结论

合并活跃进展性 MS 的患者表现出炎症、脱髓鞘和神经元/轴突损伤的证据,而其余患者主要表现出活跃脱髓鞘的证据。这对独立于炎症的神经退行性变在疾病进展中至关重要的观点提出了挑战。

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