Neurology Department, APHM, Reference Center for Neuromuscular Diseases and ALS, La Timone University Hospital, Aix-Marseille University, Marseille, France.
CNRS, Center for Magnetic Resonance in Biology, UMR 7339, Aix-Marseille University, Marseille, France.
Eur J Neurol. 2020 Aug;27(8):1382-1389. doi: 10.1111/ene.14303. Epub 2020 Jun 3.
Nerve tissue alterations have rarely been quantified in Charcot-Marie-Tooth type 1A (CMT1A) patients. The aim of the present study was to quantitatively assess the magnetic resonance imaging (MRI) anomalies of the sciatic and tibial nerves in CMT1A disease using quantitative neurography MRI. It was also intended to seek for correlations with clinical variables.
Quantitative neurography MRI was used in order to assess differences in nerve volume, proton density and magnetization transfer ratio in the lower limbs of CMT1A patients and healthy controls. Disease severity was evaluated using the Charcot-Marie-Tooth Neuropathy Score version 2, Charcot-Marie-Tooth examination scores and Overall Neuropathy Limitations Scale scores. Electrophysiological measurements were performed in order to assess the compound motor action potential and the Motor Unit Number Index. Clinical impairment was evaluated using muscle strength measurements and Charcot-Marie-Tooth examination scores.
A total of 32 CMT1A patients were enrolled and compared to 13 healthy subjects. The 3D nerve volume, magnetization transfer ratio and proton density were significantly different in CMT1A patients for the whole sciatic and tibial nerve volume. The sciatic nerve volume was significantly correlated with the whole set of clinical scores whereas no correlation was found between the tibial nerve volume and the clinical scores.
Nerve injury could be quantified in vivo using quantitative neurography MRI and the corresponding biomarkers were correlated with clinical disability in CMT1A patients. The sensitivity of the selected metrics will have to be assessed through repeated measurements over time during longitudinal studies to evaluate structural nerve changes under treatment.
很少有研究对 1 型遗传性运动感觉神经病(CMT1A)患者的神经组织改变进行定量评估。本研究旨在使用定量神经磁共振成像(MRI)评估 CMT1A 患者坐骨神经和胫神经的 MRI 异常,并寻找与临床变量的相关性。
使用定量神经磁共振成像来评估 CMT1A 患者和健康对照组下肢神经体积、质子密度和磁化转移率的差异。使用 2 版 Charcot-Marie-Tooth 神经病评分、Charcot-Marie-Tooth 检查评分和总体神经功能障碍量表评分评估疾病严重程度。进行电生理学测量以评估复合运动动作电位和运动单位数量指数。使用肌肉力量测量和 Charcot-Marie-Tooth 检查评分评估临床损伤。
共纳入 32 例 CMT1A 患者,并与 13 例健康受试者进行比较。CMT1A 患者的整个坐骨神经和胫神经体积的 3D 神经体积、磁化转移率和质子密度均有显著差异。坐骨神经体积与所有临床评分显著相关,而胫神经体积与临床评分无相关性。
可以使用定量神经磁共振成像对神经损伤进行体内定量评估,并且相关生物标志物与 CMT1A 患者的临床残疾相关。在纵向研究中,需要通过重复测量评估选定指标的敏感性,以评估治疗期间的结构性神经变化。