Division of Allergology, Pulmonology and Cystic Fibrosis, Department for Children and Adolescents, Goethe University, Frankfurt, Germany.
Division of Pediatric Neurology, Department for Children and Adolescents, Goethe University, Frankfurt, Germany.
Cerebellum. 2022 Feb;21(1):39-47. doi: 10.1007/s12311-021-01257-4. Epub 2021 Apr 24.
Ataxia telangiectasia (A-T) is a progressive and life-limiting disease associated with cerebellar ataxia due to progressive cerebellar degeneration. In addition to ataxia, which is described in detail, the presence of chorea, dystonia, oculomotor apraxia, athetosis, parkinsonism, and myoclonia are typical manifestations of the disease. The study aimed to evaluate the specificity and sensitivity of neurofilament light chain (NfL) as a biomarker of neurodegeneration in relation to SARA score. In this prospective trial, one visit of 42 A-T patients aged 1.3-25.6 years (mean 11.6 ± 7.3 years) was performed, in which NfL was determined from serum by ELISA. Additionally, a neurological examination of the patients was performed. Blood was collected from 19 healthy volunteers ≥ 12 years of age. We found significantly increased levels of NfL in patients with A-T compared to healthy controls (21.5 ± 3.6 pg/mL vs. 9.3 ± 0.49 pg/mL, p ≤ 0.01). There was a significant correlation of NfL with age, AFP, and SARA. NfL is a new potential progression biomarker in blood for neurodegeneration in A-T which increases with age.
共济失调毛细血管扩张症(A-T)是一种进行性、危及生命的疾病,由于小脑进行性变性,导致小脑共济失调。除了详细描述的共济失调外,舞蹈病、肌张力障碍、眼球运动不能、手足徐动症、帕金森病和肌阵挛也是该病的典型表现。本研究旨在评估神经丝轻链(NfL)作为与 SARA 评分相关的神经退行性变生物标志物的特异性和敏感性。在这项前瞻性试验中,对 42 名年龄在 1.3-25.6 岁(平均 11.6 ± 7.3 岁)的 A-T 患者进行了一次就诊,通过 ELISA 从血清中测定 NfL。此外,对患者进行了神经系统检查。从≥ 12 岁的 19 名健康志愿者中采集血液。与健康对照组相比,A-T 患者的 NfL 水平显著升高(21.5 ± 3.6 pg/mL 比 9.3 ± 0.49 pg/mL,p ≤ 0.01)。NfL 与年龄、AFP 和 SARA 呈显著相关性。NfL 是血液中 A-T 神经退行性变的一种新的潜在进展生物标志物,其水平随年龄增长而增加。