Wilke Carlo, Rattay Tim W, Hengel Holger, Zimmermann Milan, Brockmann Kathrin, Schöls Ludger, Kuhle Jens, Schüle Rebecca, Synofzik Matthis
Department of Neurodegenerative Diseases Hertie-Institute for Clinical Brain Research and Center of Neurology University of Tübingen Hoppe-Seyler-Str. 3 72076 Tübingen Germany.
German Center for Neurodegenerative Diseases (DZNE) Tübingen Germany.
Ann Clin Transl Neurol. 2018 May 21;5(7):876-882. doi: 10.1002/acn3.583. eCollection 2018 Jul.
Blood biomarkers are still largely missing in hereditary spastic paraplegias (HSPs). We here explored Neurofilament light chain (NfL) as a biomarker in HSP. Serum NfL was assessed in 96 HSP (63 genetically confirmed), 96 healthy control, and 33 ALS subjects by single molecule array (Simoa). Compared to controls, NfL was increased in HSP ( < 0.001), correlating with cross-sectional disease progression ( = 0.28). Levels were lower than in ALS ( < 0.001), allowing to differentiate HSP from ALS (AUC = 0.91). Serum NfL might serve as a biomarker in HSP indicating neuronal damage and, if confirmed longitudinally, disease progression. It might also support differentiating HSP from ALS.
血液生物标志物在遗传性痉挛性截瘫(HSP)中仍大多缺失。我们在此探索神经丝轻链(NfL)作为HSP的一种生物标志物。通过单分子阵列(Simoa)对96例HSP患者(63例经基因确认)、96例健康对照者和33例肌萎缩侧索硬化(ALS)患者的血清NfL进行了评估。与对照组相比,HSP患者的NfL升高(<0.001),与疾病的横断面进展相关(=0.28)。其水平低于ALS患者(<0.001),有助于将HSP与ALS区分开来(曲线下面积=0.91)。血清NfL可能作为HSP的一种生物标志物,表明神经元损伤,若经纵向研究得到证实,还可表明疾病进展。它也可能有助于区分HSP与ALS。