Increase of Plasma Biomarkers in Friedreich's Ataxia: Potential Insights into Disease Pathology.

IF 7.6
Christian Rummey, Gilbert Thomas-Black, Hector Garcia-Moreno, David R Lynch, Rosella Abeti, Huseyin Arisoy, Amanda Heslegrave, Henrik Zetterberg, Paola Giunti
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Abstract

Background: Therapeutic interventions in Friedreich's ataxia (FRDA) are progressing into clinical trials, and the need for robust and easily accessible biomarkers has arisen.

Objective: This study aimed to consolidate preliminary findings of changes in the levels of neurofilament light (NfL), glial fibrillary acidic protein (GFAP), Tau, and ubiquitin C-terminal hydrolase L1(UCH-L1) in FRDA comparing two large independent cohorts of patients with healthy controls.

Methods: Plasma samples of patients from two large natural history studies (n = 187) and a similar sized cohort of healthy control subjects (n = 127) were assessed using single-molecule array measurements. Age-adjusted biomarker levels were related to patients' genetic profile, clinical progression, and comorbidities, and compared with controls. Sensitivity and specificity were assessed using receiver operating characteristic analyses.

Results: NfL levels were significantly elevated in patients with FRDA younger than 40 years, showing a distinct age-dependent trajectory: levels declined with age in FRDA but increased in controls. Longitudinal data indicated annual NfL reductions between 8% (children) and 13% (young adults < 35 years). This result is discussed in the context of other neurodegenerative conditions, with FRDA being a rare case where NfL levels decrease over time before the age of 40 years. In contrast, tau was consistently elevated across all age groups in FRDA.

Conclusions: NfL is a sensitive biomarker in early FRDA but decreases with age, converging with control values after 35-40 years. This age-dependent pattern must be considered when interpreting the effect of interventions in clinical trials. Especially in younger (age < 10 years) or presymptomatic patients and control subjects, additional longitudinal sampling is warranted. Elevated tau levels suggest involvement in underlying disease pathophysiology. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

血浆生物标志物在弗里德赖希共济失调中的增加:对疾病病理学的潜在见解。
背景:弗里德赖希共济失调(FRDA)的治疗干预措施正在进入临床试验阶段,对强大且易于获取的生物标志物的需求已经出现。目的:本研究旨在巩固FRDA中神经丝光(NfL)、胶质纤维酸性蛋白(GFAP)、Tau和泛素c端水解酶L1(UCH-L1)水平变化的初步发现,并将两组独立的健康对照患者进行比较。方法:采用单分子阵列测量方法,对来自两项大型自然史研究(n = 187)和类似规模的健康对照受试者(n = 127)的血浆样本进行评估。与对照组相比,年龄调整的生物标志物水平与患者的遗传谱、临床进展和合并症有关。采用受试者工作特征分析评估敏感性和特异性。结果:在年龄小于40岁的FRDA患者中,NfL水平显著升高,表现出明显的年龄依赖轨迹:FRDA患者中,NfL水平随着年龄的增长而下降,而对照组中则升高。纵向数据显示,NfL每年减少8%(儿童)至13%(年轻人)。结论:NfL是早期FRDA的敏感生物标志物,但随着年龄的增长而下降,在35-40岁后与对照组趋同。在临床试验中解释干预措施的效果时,必须考虑到这种年龄依赖模式。尤其是在年轻的时候
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