From the Department of Neurology (M.R., E.T., G.C.), Nîmes University Hospital Center, Univ. Montpellier; Functional Genomics Institute (M.R., E.T., L.D.T.T., P.M.), Univ. Montpellier, CNRS, INSERM; Department of Biostatistics (S.L.-C., C.D., T.M.), Clinical Epidemiology, Public Health and Innovation in Methdology (BESPIM), Nîmes University Hospital Center, Univ. Montpellier, France; Department of Neurology (U.U., A.S.), Cerrahpasa School of Medecine, University of Istanbul, Turkey; Centre de Ressources et Compétences Sclérose En Plaques (CRCSEP) (M.C., C.L.-F.), CHU de Nice, Hôpital Pasteur 2, Université Côte d'Azur, UR2CA-URRIS, France; UT Southwestern Medical Center (D.T.O.), Dallas, TX; Mayo Clinic (O.H.K.), Rochester, MN; University of South California (D.P., C.A.), Los Angeles; and LBPC-PPC (S.L.), Univ. Montpellier, CHU Montpellier, INM, INSERM, France.
Neurol Neuroimmunol Neuroinflamm. 2022 Oct 24;10(1). doi: 10.1212/NXI.0000000000200044. Print 2023 Jan.
To evaluate the predictive value of serum neurofilament light chain (sNfL) and CSF NfL (cNfL) in patients with radiologically isolated syndrome (RIS) for evidence of disease activity (EDA) and clinical conversion (CC).
sNfL and cNfL were measured at RIS diagnosis by single-molecule array (Simoa). The risk of EDA and CC according to sNfL and cNfL was evaluated using the Kaplan-Meier analysis and multivariate Cox regression models including age, spinal cord (SC) or infratentorial lesions, oligoclonal bands, CSF chitinase 3-like protein 1, and CSF white blood cells.
Sixty-one patients with RIS were included. At diagnosis, sNfL and cNfL were correlated (Spearman r = 0.78, < 0.001). During follow-up, 47 patients with RIS showed EDA and 36 patients showed CC (median time 12.6 months, 1-86). When compared with low levels, medium and high cNfL (>260 pg/mL) and sNfL (>5.0 pg/mL) levels were predictive of EDA (log rank, < 0.01 and = 0.02, respectively). Medium-high cNfL levels were predictive of CC (log rank, < 0.01). In Cox regression models, cNfL and sNfL were independent factors of EDA, while SC lesions, cNfL, and sNfL were independent factors of CC.
cNfL >260 pg/mL and sNfL >5.0 pg/mL at diagnosis are independent predictive factors of EDA and CC in RIS. Although cNfL predicts disease activity better, sNfL is more accessible than cNfL and can be considered when a lumbar puncture is not performed.
This study provides Class II evidence that in people with radiologic isolated syndrome (RIS), initial serum and CSF NfL levels are associated with subsequent evidence of disease activity or clinical conversion.
评估血清神经丝轻链(sNfL)和脑脊液神经丝轻链(cNfL)在放射学孤立综合征(RIS)患者中的预测价值,以评估其是否存在疾病活动(EDA)和临床转化(CC)的证据。
通过单分子阵列(Simoa)在 RIS 诊断时测量 sNfL 和 cNfL。采用 Kaplan-Meier 分析和多变量 Cox 回归模型评估 sNfL 和 cNfL 与 EDA 和 CC 的风险,该模型包括年龄、脊髓(SC)或颅后窝病变、寡克隆带、脑脊液几丁质酶 3 样蛋白 1 和脑脊液白细胞。
共纳入 61 例 RIS 患者。在诊断时,sNfL 和 cNfL 呈正相关(Spearman r = 0.78, < 0.001)。在随访期间,47 例 RIS 患者出现 EDA,36 例患者出现 CC(中位时间 12.6 个月,1-86)。与低水平相比,中高水平 cNfL(>260pg/mL)和 sNfL(>5.0pg/mL)水平预测 EDA 的发生(对数秩检验,分别为 < 0.01 和 = 0.02)。中高水平 cNfL 水平预测 CC(对数秩检验, < 0.01)。在 Cox 回归模型中,cNfL 和 sNfL 是 EDA 的独立因素,而 SC 病变、cNfL 和 sNfL 是 CC 的独立因素。
诊断时 cNfL >260pg/mL 和 sNfL >5.0pg/mL 是 RIS 患者 EDA 和 CC 的独立预测因素。虽然 cNfL 能更好地预测疾病活动,但 sNfL 比 cNfL 更易获得,在未行腰椎穿刺时可考虑使用。
本研究提供 II 级证据,表明在放射学孤立综合征(RIS)患者中,初始血清和脑脊液 NfL 水平与随后的疾病活动或临床转化证据相关。