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7.0T MRI 评估多发性硬化皮质病变与皮质变薄的相关性及其临床影响。

The relevance of multiple sclerosis cortical lesions on cortical thinning and their clinical impact as assessed by 7.0-T MRI.

机构信息

Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Boston, MA, USA.

Harvard Medical School, Boston, MA, USA.

出版信息

J Neurol. 2021 Jul;268(7):2473-2481. doi: 10.1007/s00415-021-10400-4. Epub 2021 Feb 1.

Abstract

OBJECTIVE

This study aimed to investigate at 7.0-T MRI a) the role of multiple sclerosis (MS) cortical lesions in cortical tissue loss b) their relation to neurological disability.

METHODS

In 76 relapsing remitting and 26 secondary progressive MS patients (N = 102) and 56 healthy subjects 7.0-T T-weighted images were acquired for lesion segmentation; 3.0-T T-weighted structural scans for cortical surface reconstruction/cortical thickness estimation. Patients were dichotomized based on the median cortical lesion volume in low and high cortical lesion load groups that differed by age, MS phenotype and degree of neurological disability. Group differences in cortical thickness were tested on reconstructed cortical surface. Patients were evaluated clinically by means of the Expanded Disability Status Scale (EDSS).

RESULTS

Cortical lesions were detected in 96% of patients. White matter lesion load was greater in the high than in the low cortical lesion load MS group (p = 0.01). Both MS groups disclosed clusters (prevalently parietal) of cortical thinning relative to healthy subjects, though these regions did not show the highest cortical lesion density, which predominantly involved frontal regions. Cortical thickness decreased on average by 0.37 mm, (p = 0.002) in MS patients for each unit standard deviation change in white matter lesion volume. The odds of having a higher EDSS were associated with cortical lesion volume (1.78, p = 0.01) and disease duration (1.15, p < 0.001).

CONCLUSION

Cortical thinning in MS is not directly related to cortical lesion load but rather with white matter lesion volume. Neurological disability in MS is better explained by cortical lesion volume assessment.

摘要

目的

本研究旨在 7.0-T MRI 上探讨 a) 多发性硬化(MS)皮质病变在皮质组织丢失中的作用 b) 它们与神经功能障碍的关系。

方法

在 76 例复发缓解型和 26 例继发进展型 MS 患者(N=102)和 56 例健康对照者中,采集了 7.0-T T1 加权图像以进行病变分割;采集 3.0-T T1 加权结构扫描以进行皮质表面重建/皮质厚度估计。根据皮质病变体积中位数将患者分为低皮质病变负荷组和高皮质病变负荷组,两组在年龄、MS 表型和神经功能障碍程度方面存在差异。在重建的皮质表面上测试了皮质厚度的组间差异。通过扩展残疾状况量表(EDSS)对患者进行临床评估。

结果

皮质病变在 96%的患者中被检测到。高皮质病变负荷组的白质病变负荷大于低皮质病变负荷组(p=0.01)。与健康对照组相比,两组 MS 患者均显示出皮质变薄的簇(主要位于顶叶),尽管这些区域并未显示出最高的皮质病变密度,而这些病变主要累及额叶区域。皮质厚度平均减少了 0.37 毫米(p=0.002),每单位标准差白质病变体积变化,MS 患者的皮质厚度就会减少。皮质病变体积(1.78,p=0.01)和疾病持续时间(1.15,p<0.001)与较高的 EDSS 几率相关。

结论

MS 中的皮质变薄与皮质病变负荷无关,而是与白质病变体积有关。MS 中的神经功能障碍可以通过皮质病变体积评估得到更好的解释。

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