Geraldo Ana Filipa, Pereira João, Nunes Pedro, Reimão Sofia, Sousa Rita, Castelo-Branco Miguel, Pinto Susana, Campos Jorge Guedes, de Carvalho Mamede
Department of Neuroradiology, CHLN-Hospital de Santa Maria, Lisbon, Portugal.
Department of Radiology, Neuroradiology Unit, CHVNG/E-Centro Hospitalar Vila Nova de Gaia, Espinho, Portugal.
Neuroradiology. 2018 May;60(5):505-515. doi: 10.1007/s00234-018-2012-6. Epub 2018 Mar 22.
This paper aims to analyze the contribution of mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD) in the detection of microstructural abnormalities in amyotrophic lateral sclerosis (ALS) and to evaluate the degree of agreement between structural and functional changes through concomitant diffusion tensor imaging (DTI), transcranial magnetic stimulation (TMS), and clinical assessment.
Fourteen patients with ALS and 11 healthy, age- and gender-matched controls were included. All participants underwent magnetic resonance imaging including DTI. TMS was additionally performed in ALS patients. Differences in the distribution of DTI-derived measures were assessed using tract-based spatial statistical (TBSS) and volume of interest (VOI) analyses. Correlations between clinical, imaging, and neurophysiological findings were also assessed through TBSS.
ALS patients showed a significant increase in AD and MD involving the corticospinal tract (CST) and the pre-frontal white matter in the right posterior limb of the internal capsule (p < 0.05) when compared to the control group using TBSS, confirmed by VOI analyses. VOI analyses also showed increased AD in the corpus callosum (p < 0.05) in ALS patients. Fractional anisotropy (FA) in the right CST correlated significantly with upper motor neuron (UMN) score (r = - 0.79, p < 0.05), and right abductor digiti minimi central motor conduction time was highly correlated with RD in the left posterior internal capsule (r = - 0.81, p < 0.05). No other significant correlation was found.
MD, AD, and RD, besides FA, are able to further detect and characterize neurodegeneration in ALS. Furthermore, TMS and DTI appear to have a role as complementary diagnostic biomarkers of UMN dysfunction.
本文旨在分析平均扩散率(MD)、轴向扩散率(AD)和径向扩散率(RD)在检测肌萎缩侧索硬化症(ALS)微观结构异常中的作用,并通过同步扩散张量成像(DTI)、经颅磁刺激(TMS)和临床评估来评估结构与功能变化之间的一致性程度。
纳入14例ALS患者以及11名年龄和性别匹配的健康对照者。所有参与者均接受了包括DTI在内的磁共振成像检查。ALS患者还额外接受了TMS检查。使用基于纤维束的空间统计学(TBSS)和感兴趣区(VOI)分析评估DTI衍生测量值分布的差异。还通过TBSS评估临床、影像学和神经生理学结果之间的相关性。
与对照组相比,使用TBSS分析显示,ALS患者在皮质脊髓束(CST)以及右侧内囊后肢的前额叶白质中,AD和MD显著增加(p < 0.05),VOI分析证实了这一点。VOI分析还显示,ALS患者胼胝体中的AD增加(p < 0.05)。右侧CST中的分数各向异性(FA)与上运动神经元(UMN)评分显著相关(r = -0.79,p < 0.05),右侧小指展肌中枢运动传导时间与左侧内囊后肢的RD高度相关(r = -0.81,p < 0.05)。未发现其他显著相关性。
除FA外,MD、AD和RD能够进一步检测和表征ALS中的神经退行性变。此外,TMS和DTI似乎可作为UMN功能障碍的补充诊断生物标志物。