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进展性多发性硬化症与肌萎缩侧索硬化症中的灰质损伤:基于体素的形态测量MRI研究

Grey matter damage in progressive multiple sclerosis versus amyotrophic lateral sclerosis: a voxel-based morphometry MRI study.

作者信息

Tavazzi Eleonora, Laganà Maria Marcella, Bergsland Niels, Tortorella Paola, Pinardi Giovanna, Lunetta Christian, Corbo Massimo, Rovaris Marco

机构信息

Unit of Motor Neurorehabilitation, Multiple Sclerosis Center, Scientific Institute Santa Maria Nascente, Fondazione Don Gnocchi, via Capecelatro 66, 20148, Milan, Italy.

出版信息

Neurol Sci. 2015 Mar;36(3):371-7. doi: 10.1007/s10072-014-1954-7. Epub 2014 Sep 17.

Abstract

Primary progressive multiple sclerosis (PPMS) and amyotrophic lateral sclerosis (ALS) seem to share some clinical and pathological features. MRI studies revealed the presence of grey matter (GM) atrophy in both diseases, but no comparative data are available. The objective was to compare the regional patterns of GM tissue loss in PPMS and ALS with voxel-based morphometry (VBM). Eighteen PPMS patients, 20 ALS patients, and 31 healthy controls (HC) were studied with a 1.5 Tesla scanner. VBM was performed to assess volumetric GM differences with age and sex as covariates. Threshold-free cluster enhancement analysis was used to obtain significant clusters. Group comparisons were tested with family-wise error correction for multiple comparisons (p < 0.05) except for HC versus MND which was tested at a level of p < 0.001 uncorrected and a cluster threshold of 20 contiguous voxels. Compared to HC, ALS patients showed GM tissue reduction in selected frontal and temporal areas, while PPMS patients showed a widespread bilateral GM volume decrease, involving both deep and cortical regions. Compared to ALS, PPMS patients showed tissue volume reductions in both deep and cortical GM areas. This preliminary study confirms that PPMS is characterized by a more diffuse cortical and subcortical GM atrophy than ALS and that, in the latter condition, brain damage is present outside the motor system. These results suggest that PPMS and ALS may share pathological features leading to GM tissue loss.

摘要

原发性进行性多发性硬化症(PPMS)和肌萎缩侧索硬化症(ALS)似乎具有一些临床和病理特征。MRI研究显示这两种疾病均存在灰质(GM)萎缩,但尚无比较数据。目的是通过基于体素的形态学测量(VBM)比较PPMS和ALS中GM组织丢失的区域模式。对18例PPMS患者、20例ALS患者和31名健康对照者(HC)使用1.5特斯拉扫描仪进行研究。采用VBM评估以年龄和性别作为协变量的GM体积差异。使用无阈值聚类增强分析来获得显著聚类。除HC与运动神经元疾病(MND)的比较在未校正的p < 0.001水平和20个连续体素的聚类阈值下进行检验外,组间比较采用家族性错误校正进行多重比较(p < 0.05)。与HC相比,ALS患者在选定的额叶和颞叶区域显示GM组织减少,而PPMS患者显示双侧GM体积广泛减少,累及深部和皮质区域。与ALS相比,PPMS患者在深部和皮质GM区域的组织体积均减少。这项初步研究证实,与ALS相比,PPMS的特征是皮质和皮质下GM萎缩更为弥漫,并且在ALS这种情况下,脑损伤存在于运动系统之外。这些结果表明,PPMS和ALS可能具有导致GM组织丢失的共同病理特征。

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