Neuroimaging Research Unit, Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan 20132, Italy.
Mult Scler. 2013 Apr;19(4):418-26. doi: 10.1177/1352458512457842. Epub 2012 Aug 20.
Pathologic and magnetic resonance imaging (MRI) studies have shown that cortical lesions (CLs) are a frequent finding in multiple sclerosis (MS).
To quantify microstructural damage in CLs and normal appearing (NA) cortex in relapse-onset MS patients at different stages of the disease.
Brain double inversion recovery (DIR), diffusion tensor (DT) MRI and 3D T 1-weighted scans were acquired from 35 relapsing-remitting (RR) patients, 23 secondary progressive (SP) patients, 12 benign (B) MS patients and 41 healthy controls (HC). Diffusivity values in CLs, cortex, white matter (WM) lesions and normal-appearing white matter (NAWM) were assessed.
Compared to HC, MS patients had a significantly lower fractional anisotropy (FA) and higher mean diffusivity (MD) in the cortex and NAWM. CLs had higher FA vs HC cortex and vs patients' cortex. Compared to RRMS patients, SPMS patients had higher WM lesion volume, higher MD in the cortex, and more severe damage to the NAWM and WM lesions. Compared to SPMS patients, BMS patients had lower MD and FA of CLs. Damage in other compartments was similar between SPMS and BMS patients. Damage in CLs had a high power to discriminate BMS from SPMS (area under the curve: 79-91%), with high specificity (85%), sensitivity (100%) and accuracy (90%).
Microstructural imaging features of CLs differ from those of WM lesions and are likely to reflect neuronal damage and microglial activation. The nature and extent of CL damage can be used to help distinguish the different MS clinical phenotypes.
病理和磁共振成像(MRI)研究表明,皮质病变(CLs)是多发性硬化症(MS)的常见发现。
在不同疾病阶段的复发缓解型 MS 患者中,定量分析 CL 和正常外观(NA)皮质的微观结构损伤。
对 35 例复发缓解型(RR)患者、23 例继发进展型(SP)患者、12 例良性(B)MS 患者和 41 例健康对照者(HC)进行脑双反转恢复(DIR)、弥散张量(DT)MRI 和 3D T1 加权扫描。评估 CL、皮质、白质(WM)病变和正常外观白质(NAWM)中的扩散值。
与 HC 相比,MS 患者皮质和 NAWM 的各向异性分数(FA)显著降低,平均弥散度(MD)升高。CL 的 FA 高于 HC 皮质和患者皮质。与 RRMS 患者相比,SPMS 患者的 WM 病变体积更高,皮质 MD 更高,且 NAWM 和 WM 病变损伤更严重。与 SPMS 患者相比,BMS 患者的 CL 具有更低的 MD 和 FA。SPMS 和 BMS 患者的其他部位损伤相似。CL 损伤在区分 BMS 和 SPMS 方面具有较高的辨别能力(曲线下面积:79-91%),具有较高的特异性(85%)、敏感性(100%)和准确性(90%)。
CL 的微观结构成像特征与 WM 病变不同,可能反映神经元损伤和小胶质细胞激活。CL 损伤的性质和程度可用于帮助区分不同的 MS 临床表型。