Department of Neurology, University of Ulm, Ulm, Germany.
Department of Pharmacology and Clinical Neuroscience, Umeå University, Umeå, Sweden.
J Neurol Neurosurg Psychiatry. 2016 Jan;87(1):12-20. doi: 10.1136/jnnp-2015-311387. Epub 2015 Aug 21.
Biomarkers for the diagnosis of motoneuron diseases (MND) are urgently needed to improve the diagnostic pathway, patient stratification and monitoring. The aim of this study was to validate candidate markers for MND in cerebrospinal fluid (CSF) and specify cut-offs based on large patient cohorts by especially considering patients who were seen under the initial differential diagnosis (MND mimics).
In a prospective study, we investigated CSF of 455 patients for neurofilament light chain (NfL), phosphorylated heavy chain (pNfH), tau protein (Tau) and phospho-tau protein (pTau). Analysed cohorts included patients with apparently sporadic and familial amyotrophic lateral sclerosis (ALS) and primary lateral sclerosis (PLS) (MND, n=253), MND mimics (n=85) and neurological control groups. Cut-off values were specified, and diagnostic performance and correlation with progression were analysed.
Nfs were significantly higher in the MND group compared to the control groups, whereas Tau and pTau did not differ. At a cut-off level of 2200 pg/mL for NfL, a 77% diagnostic sensitivity (CI 71% to 82%), 85% specificity (CI 79% to 90%) and 87% positive predictive value (PPV) (CI 81% to 91%) were achieved. For pNfH, we calculated 83% sensitivity (CI 78% to 88%), 77% specificity (CI 71% to 83%) and 82% PPV (CI 77% to 86%) at 560 pg/mL. There were no significant differences between sporadic and genetic ALS or PLS. Nf levels were elevated at early disease stage, and correlated moderately with MND progression and duration.
Neurofilaments in CSF have a high relevance for the differential diagnosis of MNDs and should be included in the diagnostic work-up of patients. Their value as prognostic markers should be investigated further.
运动神经元病(MND)的诊断生物标志物对于改善诊断途径、患者分层和监测至关重要。本研究旨在通过特别是考虑初始鉴别诊断(MND 模拟物)下的患者,验证脑脊液(CSF)中候选 MND 标志物,并根据大型患者队列确定截止值。
在一项前瞻性研究中,我们研究了 455 例患者的神经丝轻链(NfL)、磷酸化重链(pNfH)、tau 蛋白(Tau)和磷酸化 tau 蛋白(pTau)的 CSF。分析队列包括明显散发和家族性肌萎缩侧索硬化症(ALS)和原发性侧索硬化症(PLS)(MND,n=253)、MND 模拟物(n=85)和神经学对照组。指定了截断值,并分析了诊断性能和与进展的相关性。
与对照组相比,MND 组的 Nfs 明显升高,而 Tau 和 pTau 没有差异。在 NfL 的截断值为 2200pg/mL 时,诊断敏感性为 77%(CI 71%至 82%),特异性为 85%(CI 79%至 90%),阳性预测值(PPV)为 87%(CI 81%至 91%)。对于 pNfH,我们计算出在 560pg/mL 时,敏感性为 83%(CI 78%至 88%),特异性为 77%(CI 71%至 83%),PPV 为 82%(CI 77%至 86%)。散发型和遗传性 ALS 或 PLS 之间没有显著差异。Nf 水平在疾病早期升高,与 MND 进展和持续时间中度相关。
CSF 中的神经丝对 MND 的鉴别诊断具有重要意义,应纳入患者的诊断评估。它们作为预后标志物的价值应进一步研究。