Abstract

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.

Highlights

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

  • Our most salient finding is that the serum NfL level is elevated in AD Spinocerebellar ataxia (SCA) patients and is correlated with the clinical severity markers of AD SCA such as trinucleotide repeat number, disease duration, disease duration/ age × trinucleotide repeat number, and clinical severity (SARA score)

  • Since disease severity and the rate of progression in AD SCA are quite heterogeneous among different types and i­ndividuals[1,2], a reliable and measurable biomarker could be helpful for monitoring disease progression, evaluating treatment responses, and predicting ­prognosis[1,4,15]

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Summary

Introduction

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). This study shows that serum NfL is elevated in AD SCA patients and correlates with clinical severity. A biomarker is needed to track disease ­progression[1,4] Clinical severity scales, such as the Scale for the Assessment and Rating of Ataxia (SARA)[5], are widely used to assess disease progression. We aimed to determine whether serum NfL could be a biomarker indicating clinical severity in AD SCA. To demonstrate this hypothesis, we measured the serum NfL levels in various types of AD SCA patients and compared them to the controls. We evaluated the correlation between serum NfL and clinical severity

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