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Serum neurofilament light chain as a severity marker for spinocerebellar ataxia

Since the serum neurofilament light (NfL) chain is known as a promising biomarker in neurodegenerative diseases, we aimed to evaluate serum NfL as a biomarker indicating neuronal damage in autosomal-dominant (AD) spinocerebellar ataxia (SCA). We reviewed patients diagnosed with AD SCA in the outpati...

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Autores principales: Shin, Hye-Rim, Moon, Jangsup, Lee, Woo-Jin, Lee, Han Sang, Kim, Eun Young, Shin, Seoyi, Lee, Soon-Tae, Jung, Keun-Hwa, Park, Kyung-Il, Jung, Ki-Young, Lee, Sang Kun, Chu, Kon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241827/
https://www.ncbi.nlm.nih.gov/pubmed/34188109
http://dx.doi.org/10.1038/s41598-021-92855-z
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author Shin, Hye-Rim
Moon, Jangsup
Lee, Woo-Jin
Lee, Han Sang
Kim, Eun Young
Shin, Seoyi
Lee, Soon-Tae
Jung, Keun-Hwa
Park, Kyung-Il
Jung, Ki-Young
Lee, Sang Kun
Chu, Kon
author_facet Shin, Hye-Rim
Moon, Jangsup
Lee, Woo-Jin
Lee, Han Sang
Kim, Eun Young
Shin, Seoyi
Lee, Soon-Tae
Jung, Keun-Hwa
Park, Kyung-Il
Jung, Ki-Young
Lee, Sang Kun
Chu, Kon
author_sort Shin, Hye-Rim
collection PubMed
description Since the serum neurofilament light (NfL) chain is known as a promising biomarker in neurodegenerative diseases, we aimed to evaluate serum NfL as a biomarker indicating neuronal damage in autosomal-dominant (AD) spinocerebellar ataxia (SCA). We reviewed patients diagnosed with AD SCA in the outpatient clinic of Seoul National University Hospital’s (SNUH) Department of Neurology between May and August of 2019. We reviewed the demographic data, clinical characteristics, Scale for the Assessment and Rating of Ataxia (SARA) score, and brain magnetic resonance imaging (MRI) scans. The serum NfL was measured by electrochemiluminescence (ECL) immunoassay. Forty-nine patients with AD SCA were reviewed and their serum NfL level was determined. The median serum NfL level (109.5 pg/mL) was higher than control (41.1 pg/mL) (p-value < 0.001). Among the AD SCA patients, there was a positive correlation between the serum NfL level and the trinucleotide repeat number (r = 0.47, p-value = 0.001), disease duration (r = 0.35, p-value = 0.019), disease duration/age × trinucleotide repeat number (r = 0.330, p-value = 0.021), and SARA score (n = 33; r = 0.37, p-value = 0.033). This study shows that serum NfL is elevated in AD SCA patients and correlates with clinical severity.
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spelling pubmed-82418272021-07-06 Serum neurofilament light chain as a severity marker for spinocerebellar ataxia Shin, Hye-Rim Moon, Jangsup Lee, Woo-Jin Lee, Han Sang Kim, Eun Young Shin, Seoyi Lee, Soon-Tae Jung, Keun-Hwa Park, Kyung-Il Jung, Ki-Young Lee, Sang Kun Chu, Kon Sci Rep Article Since the serum neurofilament light (NfL) chain is known as a promising biomarker in neurodegenerative diseases, we aimed to evaluate serum NfL as a biomarker indicating neuronal damage in autosomal-dominant (AD) spinocerebellar ataxia (SCA). We reviewed patients diagnosed with AD SCA in the outpatient clinic of Seoul National University Hospital’s (SNUH) Department of Neurology between May and August of 2019. We reviewed the demographic data, clinical characteristics, Scale for the Assessment and Rating of Ataxia (SARA) score, and brain magnetic resonance imaging (MRI) scans. The serum NfL was measured by electrochemiluminescence (ECL) immunoassay. Forty-nine patients with AD SCA were reviewed and their serum NfL level was determined. The median serum NfL level (109.5 pg/mL) was higher than control (41.1 pg/mL) (p-value < 0.001). Among the AD SCA patients, there was a positive correlation between the serum NfL level and the trinucleotide repeat number (r = 0.47, p-value = 0.001), disease duration (r = 0.35, p-value = 0.019), disease duration/age × trinucleotide repeat number (r = 0.330, p-value = 0.021), and SARA score (n = 33; r = 0.37, p-value = 0.033). This study shows that serum NfL is elevated in AD SCA patients and correlates with clinical severity. Nature Publishing Group UK 2021-06-29 /pmc/articles/PMC8241827/ /pubmed/34188109 http://dx.doi.org/10.1038/s41598-021-92855-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Shin, Hye-Rim
Moon, Jangsup
Lee, Woo-Jin
Lee, Han Sang
Kim, Eun Young
Shin, Seoyi
Lee, Soon-Tae
Jung, Keun-Hwa
Park, Kyung-Il
Jung, Ki-Young
Lee, Sang Kun
Chu, Kon
Serum neurofilament light chain as a severity marker for spinocerebellar ataxia
title Serum neurofilament light chain as a severity marker for spinocerebellar ataxia
title_full Serum neurofilament light chain as a severity marker for spinocerebellar ataxia
title_fullStr Serum neurofilament light chain as a severity marker for spinocerebellar ataxia
title_full_unstemmed Serum neurofilament light chain as a severity marker for spinocerebellar ataxia
title_short Serum neurofilament light chain as a severity marker for spinocerebellar ataxia
title_sort serum neurofilament light chain as a severity marker for spinocerebellar ataxia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241827/
https://www.ncbi.nlm.nih.gov/pubmed/34188109
http://dx.doi.org/10.1038/s41598-021-92855-z
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