Laboratoire de Biochimie Protéomique Clinique (LBPC), Université de Montpellier, CHU de Montpellier, Institut des Neurosciences de Montpellier (INM), INSERM, Montpellier, France; Département de Biochimie, Université de Montpellier, CHU de Montpellier, Montpellier, France.
Univ. Lille, Inserm, CHU Lille, UMR-S-U1172, LiCEND, Lille Neuroscience & Cognition, LabEx DISTALZ, Lille, France.
Clin Chim Acta. 2025 Jan 15;565:120007. doi: 10.1016/j.cca.2024.120007. Epub 2024 Oct 23.
Measurement of serum neurofilament light chain (sNfL) protein is becoming a key biomarker for many neurological diseases. Several immunoassays have been developed to meet these clinical needs, revealing significant differences in terms of variability and results. Here, we propose a French multicenter comparison of 5 sNfL assays.
6 replicates of 3 pools with low (10 pg/mL), medium (30 pg/mL) and high (100 pg/mL) sNfL values and one replicate of 12 samples with growing sNfL values were analyzed by six independent French clinical laboratories. The analytical performances of the sNfL blood assay (Fujirebio®) on Lumipulse G were first evaluated then compared to four other immunoassays: NF-light V2 (Quanterix®) on SiMOA HD-X, Human NF-L (Biotechne®) on Ella, R-Plex Human Neurofilament L (MSD®) on Sector 2400; manual ELISA test using Uman Diagnostic/Quanterix®.
Inter-center comparison of the Lumipulse blood assay revealed limited but significant differences in the mean sNfL values across low, medium, and high pools between each city (p < 0.001) and between the two different batches used. Coefficients of variation of pools ranged from 2.0 to 16.9 %. Z-score of sNfL results of the 12 samples ranged from -1.70 to +1.71. Inter-technique comparison showed a systematic difference of sNfL values, with a overestimation of MSD and Ella over other tests. Nonetheless, results were all significantly correlated (p < 0.001).
The automated Lumipulse assay produced comparable sNfL values across laboratories; but further adjustments are needed to harmonize sNfL results. Biologists and physicians should be aware of the variability in results between different immunoassay suppliers.
血清神经丝轻链(sNfL)蛋白的测量正在成为许多神经疾病的关键生物标志物。已经开发出几种免疫测定法来满足这些临床需求,这些方法在变异性和结果方面存在显著差异。在这里,我们提出了一项法国多中心的 5 种 sNfL 检测方法比较。
6 个法国临床实验室分别对 3 个低值(10 pg/mL)、中值(30 pg/mL)和高值(100 pg/mL)sNfL 值的 6 个重复样本和一个 sNfL 值不断增加的 12 个样本的重复样本进行分析。首先评估 Lumipulse G 上 sNfL 血液检测(Fujirebio®)的分析性能,然后与其他 4 种免疫测定法进行比较:SiMOA HD-X 上的 NF-light V2(Quanterix®)、Ella 上的 Human NF-L(Biotechne®)、Sector 2400 上的 R-Plex Human Neurofilament L(MSD®);使用 Uman Diagnostic/Quanterix®的手动 ELISA 测试。
Lumipulse 血液检测的中心间比较显示,每个城市(p < 0.001)和两个不同批次之间的低值、中值和高值样本的 sNfL 值存在有限但显著的差异。样本池的变异系数范围为 2.0 至 16.9%。12 个样本的 sNfL 结果的 Z 分数范围为-1.70 至+1.71。技术间比较显示 sNfL 值存在系统差异,MSD 和 Ella 对其他测试的估计值过高。尽管如此,所有结果均呈显著相关(p < 0.001)。
自动化的 Lumipulse 检测法在实验室之间产生了可比的 sNfL 值;但需要进一步调整以协调 sNfL 结果。生物学家和医生应该意识到不同免疫测定法供应商之间结果的可变性。