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Correlational Analysis of ALS Progression and Serum NfL Measured by Simoa Assay in Chinese Patients
Background: Neurofilament light chain (NFL) was believed to be a promising biomarker for the diagnosis of Amyotrophic lateral sclerosis (ALS) and disease burden evaluation. Objective: To determine the serum NFL level and its clinical relevance, including its association with disease severity [evalua...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793911/ https://www.ncbi.nlm.nih.gov/pubmed/33424740 http://dx.doi.org/10.3389/fneur.2020.579094 |
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author | Sugimoto, Kazuo Han, Yi Song, Yuebo Gao, Ying |
author_facet | Sugimoto, Kazuo Han, Yi Song, Yuebo Gao, Ying |
author_sort | Sugimoto, Kazuo |
collection | PubMed |
description | Background: Neurofilament light chain (NFL) was believed to be a promising biomarker for the diagnosis of Amyotrophic lateral sclerosis (ALS) and disease burden evaluation. Objective: To determine the serum NFL level and its clinical relevance, including its association with disease severity [evaluated by the ALS Functional Rating Scale–revised (ALSFRS-r) score and King's College staging system] and progression (evaluated by the disease progression rate (DPR) and diagnostic delay), in ALS patients in China. Method: Serum NFL levels were detected using the Single Molecule Array (Simoa) technology in 30 ALS patients and 20 healthy controls (HCs). Results: There were significantly elevated levels of serum NFL in patients with ALS than in the HCs (P < 0.001). The serum NFL levels were significantly higher in rapidly progressive ALS and patients in Stage 3 than in slowly progressive ALS and patients in Stage 2 (P(DPR) < 0.001, P(Diagnosticdelay) = 0.019; P(stage)= 0.033). Furthermore, the serum NFL levels negatively correlated with the diagnostic delay (R(2) = 0.23, P = 0.016), the ALSFRS-r score (R(2) = 0.15, P = 0.047) and disease duration (R(2) = 0.15, P = 0.034), and positively correlated with the DPR (R(2) = 0.42, P < 0.001). Conclusions: The present study preliminarily investigated the diagnostic value of serum NFL and its clinical relevance in the Chinese ALS population using the ultrasensitive Simoa technology. The results demonstrated that the level of serum NFL may become a potential biomarker for ALS diagnosis and indicate disease severity and progression. |
format | Online Article Text |
id | pubmed-7793911 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77939112021-01-09 Correlational Analysis of ALS Progression and Serum NfL Measured by Simoa Assay in Chinese Patients Sugimoto, Kazuo Han, Yi Song, Yuebo Gao, Ying Front Neurol Neurology Background: Neurofilament light chain (NFL) was believed to be a promising biomarker for the diagnosis of Amyotrophic lateral sclerosis (ALS) and disease burden evaluation. Objective: To determine the serum NFL level and its clinical relevance, including its association with disease severity [evaluated by the ALS Functional Rating Scale–revised (ALSFRS-r) score and King's College staging system] and progression (evaluated by the disease progression rate (DPR) and diagnostic delay), in ALS patients in China. Method: Serum NFL levels were detected using the Single Molecule Array (Simoa) technology in 30 ALS patients and 20 healthy controls (HCs). Results: There were significantly elevated levels of serum NFL in patients with ALS than in the HCs (P < 0.001). The serum NFL levels were significantly higher in rapidly progressive ALS and patients in Stage 3 than in slowly progressive ALS and patients in Stage 2 (P(DPR) < 0.001, P(Diagnosticdelay) = 0.019; P(stage)= 0.033). Furthermore, the serum NFL levels negatively correlated with the diagnostic delay (R(2) = 0.23, P = 0.016), the ALSFRS-r score (R(2) = 0.15, P = 0.047) and disease duration (R(2) = 0.15, P = 0.034), and positively correlated with the DPR (R(2) = 0.42, P < 0.001). Conclusions: The present study preliminarily investigated the diagnostic value of serum NFL and its clinical relevance in the Chinese ALS population using the ultrasensitive Simoa technology. The results demonstrated that the level of serum NFL may become a potential biomarker for ALS diagnosis and indicate disease severity and progression. Frontiers Media S.A. 2020-12-03 /pmc/articles/PMC7793911/ /pubmed/33424740 http://dx.doi.org/10.3389/fneur.2020.579094 Text en Copyright © 2020 Sugimoto, Han, Song and Gao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Sugimoto, Kazuo Han, Yi Song, Yuebo Gao, Ying Correlational Analysis of ALS Progression and Serum NfL Measured by Simoa Assay in Chinese Patients |
title | Correlational Analysis of ALS Progression and Serum NfL Measured by Simoa Assay in Chinese Patients |
title_full | Correlational Analysis of ALS Progression and Serum NfL Measured by Simoa Assay in Chinese Patients |
title_fullStr | Correlational Analysis of ALS Progression and Serum NfL Measured by Simoa Assay in Chinese Patients |
title_full_unstemmed | Correlational Analysis of ALS Progression and Serum NfL Measured by Simoa Assay in Chinese Patients |
title_short | Correlational Analysis of ALS Progression and Serum NfL Measured by Simoa Assay in Chinese Patients |
title_sort | correlational analysis of als progression and serum nfl measured by simoa assay in chinese patients |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793911/ https://www.ncbi.nlm.nih.gov/pubmed/33424740 http://dx.doi.org/10.3389/fneur.2020.579094 |
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