Temporal profile of serum neurofilament light in multiple sclerosis: Implications for patient monitoring.

Temporal profile of serum neurofilament light in multiple sclerosis: Implications for patient monitoring.
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多发性硬化症中血清神经丝光的时间谱:对患者监测的影响。

DOI:
10.1177/1352458520972573
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发表时间:
2021-09
期刊:
Multiple sclerosis (Houndmills, Basingstoke, England)
影响因子:
--
通讯作者:
Plavina T
Plavina T
中科院分区:
其他
文献类型:
--
作者:
Calabresi PA;Arnold DL;Sangurdekar D;Singh CM;Altincatal A;de Moor C;Engle B;Goyal J;Deykin A;Szak S;Kieseier BC;Rudick RA;Plavina T

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了解纵向血清神经丝轻链(sNfL)模式如何告知其作为多发性硬化(MS)预后生物标志物的用途,并评估sNfL是否反映MS疾病活动和疾病修饰治疗的使用。这是对复发缓解型MS(RRMS)患者的ADVANCE试验(NCT 00906399)的纵向数据和样本进行的事后分析。sNfL每3个月测量一次,持续2年,然后每6个月测量一次,持续4年。回归模型探讨了sNfL数据如何预测4年的脑体积值、扩展残疾状态量表评分和T2病变。在接受安慰剂、聚乙二醇干扰素β-1a和疾病活动的患者中评估sNfL水平。基线sNfL是4年脑萎缩和新发T2病变的预测因子。与sNfL保持在<16 pg/mL的患者相比,接受聚乙二醇干扰素β-1a治疗的患者在12个月后sNfL降至<16 pg/mL,其临床(p = 0.02)和磁共振成像(MRI)(p < 0.01)结果有所改善。平均sNfL水平在聚乙二醇干扰素β-1a治疗的患者中降低,而在安慰剂治疗的患者中升高(-9.5% vs. 6.8%; p < 0.01)。这些数据支持sNfL作为RRMS的预后和疾病监测生物标志物。
To understand how longitudinal serum neurofilament light chain (sNfL) patterns can inform its use as a prognostic biomarker in multiple sclerosis (MS) and evaluate whether sNfL reflects MS disease activity and disease-modifying therapy usage. This was a post hoc analysis of longitudinal data and samples from the ADVANCE trial (NCT00906399) of patients with relapsing–remitting MS (RRMS). sNfL was measured every 3 months for 2 years, then every 6 months for 4 years. Regression models explored how sNfL data predicted 4-year values of brain volume, expanded disability status scale score, and T2 lesions. sNfL levels were assessed in those receiving placebo, peginterferon beta-1a, and those with disease activity. Baseline sNfL was a predictor of 4-year brain atrophy and development of new T2 lesions. Clinical (p = 0.02) and magnetic resonance imaging (MRI) (p < 0.01) outcomes improved in those receiving peginterferon beta-1a whose sNfL decreased to <16 pg/mL after 12 months versus those whose sNfL remained ⩾16 pg/mL. Mean sNfL levels decreased in peginterferon beta-1a-treated patients and increased in placebo-treated patients (–9.5% vs. 6.8%; p < 0.01). sNfL was higher and more variable in patients with evidence of active MS. These data support sNfL as a prognostic and disease-monitoring biomarker for RRMS.
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