Quantitation of neurofilament light chain protein in serum and cerebrospinal fluid from patients with multiple sclerosis using the MSD R-PLEX NfL assay.

IF 2.2 Q2 MEDICINE, GENERAL & INTERNAL
Diagnosis Pub Date : 2023-08-01 DOI:10.1515/dx-2022-0125
Antigona Ulndreaj, Dorsa Sohaei, Simon Thebault, Oscar D Pons-Belda, Amaia Fernandez-Uriarte, Christopher Campbell, David Cheo, Martin Stengelin, George Sigal, Mark S Freedman, Isobel A Scarisbrick, Ioannis Prassas, Eleftherios P Diamandis
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引用次数: 0

Abstract

Objectives: Neurofilament light (NfL) chain is a marker of neuroaxonal damage in various neurological diseases. Here we quantitated NfL levels in the cerebrospinal fluid (CSF) and serum from patients with multiple sclerosis (MS) and controls, using the R-PLEX NfL assay, which employs advanced Meso Scale Discovery® (MSD) electrochemiluminescence (ECL)-based detection technology.

Methods: NfL was quantitated in samples from 116 individuals from two sites (Ottawa Hospital Research Institute and Mayo Clinic), consisting of patients with MS (n=71) and age- and sex-matched inflammatory neurological controls (n=13) and non-inflammatory controls (n=32). Correlation of NfL levels between CSF and serum was assessed in paired samples in a subset of MS patients and controls (n=61). Additionally, we assessed the correlation between NfL levels obtained with MSD's R-PLEX® and Quanterix's single molecule array (Simoa®) assays in CSF and serum (n=32).

Results: Using the R-PLEX, NfL was quantitated in 99% of the samples tested, and showed a broad range in the CSF (82-500,000 ng/L) and serum (8.84-2,014 ng/L). Nf-L levels in both biofluids correlated strongly (r=0.81, p<0.0001). Lastly, Nf-L measured by MSD's R-PLEX and Quanterix's Simoa assays were highly correlated for both biofluids (CSF: r=0.94, p<0.0001; serum: r=0.95, p<0.0001).

Conclusions: We show that MSD's R-PLEX NfL assay can reliably quantitate levels of NfL in the CSF and serum from patients with MS and controls, where levels correlate strongly with Simoa.

用MSD R-PLEX NfL测定多发性硬化症患者血清和脑脊液中的神经丝轻链蛋白
目的:神经丝光(NfL)链是各种神经系统疾病中神经轴突损伤的标志。本研究采用先进的Meso Scale Discovery®(MSD)电化学发光(ECL)检测技术,使用R-PLEX NfL测定法定量了多发性硬化症(MS)患者和对照组脑脊液(CSF)和血清中的NfL水平。方法:对来自两个地点(渥太华医院研究所和梅奥诊所)的116名患者的样本进行NfL定量,其中包括MS患者(n=71),年龄和性别匹配的炎症神经对照组(n=13)和非炎症对照组(n=32)。在一组MS患者和对照组(n=61)的配对样本中,评估CSF和血清中NfL水平的相关性。此外,我们评估了用MSD的R-PLEX®和Quanterix的单分子阵列(Simoa®)测定CSF和血清中NfL水平的相关性(n=32)。结果:使用R-PLEX, 99%的检测样品中都能检测到NfL,并且在CSF (82-500,000 ng/L)和血清(8.84-2,014 ng/L)中显示出广泛的范围。结论:我们发现MSD的r - plex NfL测定可以可靠地定量MS患者和对照组CSF和血清中的NfL水平,其中NfL水平与Simoa密切相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Diagnosis
Diagnosis MEDICINE, GENERAL & INTERNAL-
CiteScore
7.20
自引率
5.70%
发文量
41
期刊介绍: Diagnosis focuses on how diagnosis can be advanced, how it is taught, and how and why it can fail, leading to diagnostic errors. The journal welcomes both fundamental and applied works, improvement initiatives, opinions, and debates to encourage new thinking on improving this critical aspect of healthcare quality.  Topics: -Factors that promote diagnostic quality and safety -Clinical reasoning -Diagnostic errors in medicine -The factors that contribute to diagnostic error: human factors, cognitive issues, and system-related breakdowns -Improving the value of diagnosis – eliminating waste and unnecessary testing -How culture and removing blame promote awareness of diagnostic errors -Training and education related to clinical reasoning and diagnostic skills -Advances in laboratory testing and imaging that improve diagnostic capability -Local, national and international initiatives to reduce diagnostic error
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