Institute of clinical Medicine, University of Oslo, Oslo, Norway/Department of Neurology, Oslo University Hospital, University of Oslo, Oslo, Norway.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway/Department of Neurology, Oslo University Hospital, Oslo, Norway; Department of Psychology, University of Oslo, Oslo, Norway.
Mult Scler. 2022 Oct;28(12):1859-1870. doi: 10.1177/13524585221097296. Epub 2022 Jun 4.
Serum neurofilament light (sNfL) chain is a promising biomarker reflecting neuro-axonal injury in multiple sclerosis (MS). However, the ability of sNfL to predict outcomes in real-world MS cohorts requires further validation.
The aim of the study is to investigate the associations of sNfL concentration, magnetic resonance imaging (MRI) and retinal optical coherence tomography (OCT) markers with disease worsening in a longitudinal European multicentre MS cohort.
MS patients ( = 309) were prospectively enrolled at four centres and re-examined after 2 years ( = 226). NfL concentration was measured by single molecule array assay in serum. The patients' phenotypes were thoroughly characterized with clinical examination, retinal OCT and MRI brain scans. The primary outcome was disease worsening at median 2-year follow-up.
Patients with high sNfL concentrations (⩾8 pg/mL) at baseline had increased risk of disease worsening at median 2-year follow-up (odds ratio (95% confidence interval) = 2.8 (1.5-5.3), = 0.001). We found no significant associations of MRI or OCT measures at baseline with risk of disease worsening.
Serum NfL concentration was the only factor associated with disease worsening, indicating that sNfL is a useful biomarker in MS that might be relevant in a clinical setting.
血清神经丝轻链(sNfL)是一种有前途的生物标志物,可反映多发性硬化症(MS)中的神经轴突损伤。然而,sNfL 预测真实世界 MS 队列中结局的能力还需要进一步验证。
本研究旨在探讨血清神经丝轻链(sNfL)浓度、磁共振成像(MRI)和视网膜光学相干断层扫描(OCT)标志物与纵向欧洲多中心 MS 队列中疾病恶化的相关性。
前瞻性纳入 4 个中心的 MS 患者(n = 309),并在 2 年后(n = 226)进行重新检查。通过单分子阵列分析法测定血清中 NfL 浓度。通过临床检查、视网膜 OCT 和大脑 MRI 扫描对患者的表型进行全面特征描述。主要结局是在中位数 2 年随访时的疾病恶化。
基线时 sNfL 浓度较高(≥8pg/mL)的患者在中位数 2 年随访时疾病恶化的风险增加(优势比(95%置信区间)= 2.8(1.5-5.3),p = 0.001)。我们发现基线时 MRI 或 OCT 测量值与疾病恶化的风险无显著相关性。
血清 NfL 浓度是唯一与疾病恶化相关的因素,表明 sNfL 是 MS 中一种有用的生物标志物,在临床环境中可能具有相关性。