Multiple Sclerosis Centre, Department of Neuroscience DNS, University Hospital, University of Padua, Padua, Italy.
Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Eur J Neurol. 2019 Aug;26(8):1068-1074. doi: 10.1111/ene.13937. Epub 2019 Mar 25.
Diffuse white matter (WM) injury is prominent in primary-progressive multiple sclerosis (PP-MS) pathology and is a potential biomarker of disease progression. Diffusion kurtosis imaging allows the quantification of non-Gaussian water diffusion, providing metrics with high WM pathological specificity. The aim of this study was to characterize the pathological changes occurring in the normal-appearing WM of patients with PP-MS at baseline and at 1-year follow-up and to assess their impact on disability and short-term disease progression.
A total of 26 patients with PP-MS and 20 healthy controls were prospectively enrolled. Diffusion kurtosis imaging single-shot echo-planar imaging (EPI) was acquired on a 3-T scanner (Philips Achieva, Best, The Netherlands) (voxel size, 2 × 2 × 2 mm , 30 directions for each b-value = 1000, 2000 s/mm and one b = 0 s/mm ). A two-compartment biophysical model of WM tract integrity was used to derive spatial maps of axonal water fraction (AWF), intra-axonal diffusivity, extra-axonal axial and radial diffusivities (D , D ) and tortuosity from the following WM tracts: corpus callosum (CC), corticospinal tract (CST) and posterior thalamic radiation (PTR).
At baseline, patients with PP-MS showed a widespread decrease of AWF, tortuosity and D and an increase of D in CC, CST and PTR (P ranging from 0.001 to 0.036). At 1-year follow-up, a significant AWF decrease was detected in the body of CC (P = 0.048), PTR (P = 0.008) and CST (P = 0.044). Baseline AWF values in CST significantly discriminated progressed from non-progressed patients (P = 0.021; area under the curve, 0.854).
Based on its change over time and its relationship with disease progression, among the analyzed metrics, AWF seems the most sensitive metric of WM tissue damage in PP-MS and therefore it could be considered as a marker for monitoring disease progression.
弥漫性白质(WM)损伤在原发性进展型多发性硬化症(PP-MS)的病理学中表现突出,是疾病进展的潜在生物标志物。扩散峰度成像可以量化非高斯水分子扩散,提供具有高 WM 病理特异性的指标。本研究旨在描述基线和 1 年随访时 PP-MS 患者正常表现 WM 中的病理变化,并评估其对残疾和短期疾病进展的影响。
前瞻性纳入 26 例 PP-MS 患者和 20 名健康对照者。在 3T 扫描仪(荷兰飞利浦 Achieva)上采集扩散峰度成像单次激发 echo-planar 成像(EPI)(体素大小 2×2×2mm,每个 b 值(b=1000、2000 s/mm 和 b=0 s/mm)采集 30 个方向)。采用 WM 束完整性的两室生物物理模型,从以下 WM 束中得出轴突水分数(AWF)、轴内弥散度、轴外轴向和径向弥散度(D、D)和迂曲度的空间图:胼胝体(CC)、皮质脊髓束(CST)和丘脑后辐射(PTR)。
基线时,PP-MS 患者的 AWF、迂曲度和 D 普遍降低,CC、CST 和 PTR 的 D 升高(P 范围为 0.001 至 0.036)。在 1 年随访时,CC 体部(P=0.048)、PTR(P=0.008)和 CST(P=0.044)的 AWF 显著下降。CST 中的基线 AWF 值可显著区分进展患者和非进展患者(P=0.021;曲线下面积为 0.854)。
基于其随时间的变化及其与疾病进展的关系,在分析的指标中,AWF 似乎是 PP-MS 中 WM 组织损伤最敏感的指标,因此可以考虑作为监测疾病进展的标志物。