Department of Neuroradiology, Heidelberg University Hospital, Heidelberg, Germany.
Department of Radiology, Hannover Medical School, Hannover, Germany.
Ann Neurol. 2017 Nov;82(5):676-685. doi: 10.1002/ana.25068. Epub 2017 Oct 26.
To detect and quantify peripheral nerve lesions in multiple sclerosis (MS) by magnetic resonance neurography (MRN).
Thirty-six patients diagnosed with MS based on the 2010 McDonald criteria (34 with the relapsing-remitting form, 2 with clinically isolated syndrome) with and without disease-modifying treatment were compared to 35 healthy age-/sex-matched volunteers. All patients underwent detailed neurological and electrophysiological examinations. Three Tesla MRN with large anatomical coverage of both legs and the lumbosacral plexus was performed by using 2-dimensional (2D) fat-saturated, T2-weighted (T2w) and dual echo turbo spin echo sequences as well as a 3D T2-weighted, fat-saturated SPACE sequence. Besides qualitative visual nerve assessment, a T2w signal quantification was performed by calculation of proton spin density and T2 relaxation time. Nerve diameter was measured as a morphometric criterion.
T2w hyperintense nerve lesions were detectable in all MS patients, with a mean lesion number at thigh level of 151.5 ± 5.7 versus 19.1 ± 2.4 in controls (p < 0.0001). Nerve proton spin density was higher in MS (tibial/peroneal: 371.8 ± 7.7/368.9 ± 8.2) versus controls (tibial/peroneal: 266.0 ± 11.0/276.8 ± 9.7, p < 0.0001). In contrast, T2 relaxation time was significantly higher in controls (tibial/peroneal: 82.0 ± 2.1/78.3 ± 1.7) versus MS (tibial/peroneal: 64.3 ± 1.0/61.2 ± 0.9, p < 0.0001). Proximal tibial and peroneal nerve caliber was higher in MS (tibial: 52.4 ± 2.1mm , peroneal: 25.4 ± 1.3mm ) versus controls (tibial: 45.2 ± 1.4mm , p < 0.0015; peroneal: 21.3 ± 0.7mm , p = 0.0049).
Peripheral nerve lesions could be visualized and quantified in MS in vivo by high-resolution MRN. Lesions are defined by an increase of proton spin density and a decrease of T2 relaxation time, indicating changes in the microstructural organization of the extracellular matrix in peripheral nerve tissue in MS. By showing involvement of the peripheral nervous system in MS, this proof-of-concept study may offer new insights into the pathophysiology and treatment of MS. Ann Neurol 2017;82:676-685.
通过磁共振神经成像(MRN)检测和量化多发性硬化症(MS)的周围神经病变。
将 36 例根据 2010 年麦克唐纳标准诊断为 MS 的患者(34 例为复发缓解型,2 例为临床孤立综合征)与未接受疾病修正治疗的患者和 35 名年龄/性别匹配的健康志愿者进行比较。所有患者均接受详细的神经学和电生理学检查。使用二维(2D)脂肪饱和 T2 加权(T2w)和双回波涡轮自旋回波序列以及三维 T2 加权、脂肪饱和 SPACE 序列进行 3T MRN,对双侧腿部和腰骶丛进行大解剖覆盖。除了定性的神经评估外,还通过质子自旋密度和 T2 弛豫时间的计算来进行 T2w 信号定量。神经直径作为形态学标准进行测量。
在所有 MS 患者中均可检测到 T2w 高信号神经病变,大腿水平的平均病变数量为 151.5±5.7 个,而对照组为 19.1±2.4 个(p<0.0001)。MS 患者的神经质子自旋密度更高(胫骨/腓骨:371.8±7.7/368.9±8.2),而对照组的神经质子自旋密度更高(胫骨/腓骨:266.0±11.0/276.8±9.7,p<0.0001)。相反,对照组的 T2 弛豫时间明显更高(胫骨/腓骨:82.0±2.1/78.3±1.7),而 MS 患者的 T2 弛豫时间则较低(胫骨/腓骨:64.3±1.0/61.2±0.9,p<0.0001)。MS 患者的胫骨和腓骨近端神经直径较大(胫骨:52.4±2.1mm,腓骨:25.4±1.3mm),而对照组的胫骨和腓骨近端神经直径较小(胫骨:45.2±1.4mm,p<0.0015;腓骨:21.3±0.7mm,p=0.0049)。
通过高分辨率 MRN 可以在 MS 患者的体内可视化和量化周围神经病变。病变的定义是质子自旋密度增加和 T2 弛豫时间减少,这表明 MS 外周神经组织细胞外基质的微观结构发生了变化。通过显示 MS 中周围神经系统的受累,这项概念验证研究可能为 MS 的病理生理学和治疗提供新的见解。神经病学年鉴 2017;82:676-685。