Department of Radiology and Nuclear Medicine, VU University Medical Center Amsterdam, The Netherlands ; Department of Neurology, Mayo Clinic 200 First St. SW, Rochester, Minnesota, 55905.
Department of Child Neurology, VU University Medical Center Amsterdam, The Netherlands.
Ann Clin Transl Neurol. 2015 Sep;2(9):932-40. doi: 10.1002/acn3.232. Epub 2015 Aug 24.
Metachromatic leukodystrophy (MLD) is an inherited lysosomal disorder due to a deficiency in arylsulfatase A with progressive demyelination and neurological decline. This retrospective MRI study investigated the extent of cortical involvement at time of diagnosis, and clinical correlates to both conventional and regional volumetric measures of brain involvement.
3D-T1-weighted MRI scans were used to determine cortical thickness and surface-based cerebral cortical gray matter (GM) and cerebral white matter (WM) volume (GMV and WMV), WM lesions, thalamus, and cerebellum. MRI-MLD severity scores were obtained from FLAIR images. Associations between clinical and imaging data were examined using correlation coefficients.
Twenty patients with MLD (mean age 13.7 years, range 2-35) and 20 controls (mean age 13.9 years, range 2-40) were included. Compared with control subjects, late-infantile, and juvenile patients (n = 14) had significantly diminished cerebral cortical GMV and thalamus volume (P < 0.05), but did not differ in WMV and cortical thickness. Adult patients (n = 6) showed significantly reduced GMV, WMV and cortical thickness (all P < 0.05). Regional analysis showed statistically significant cortical thinning in the cingulate gyrus and most pronounced thinning with age in the frontal lobe of MLD patients. Intelligence quotient (IQ) correlated with MRI-MLD scores (r = -0.87, P < 0.001).
Significant cerebral cortical GMV loss is already present in early stages of MLD. IQ correlates with WM severity scores and lesion volume, but not with volumetric measures. In adult presentations, there is more pronounced global atrophy with GMV and WMV loss and accelerated cortical thinning, most prominently in the cingulate gyrus and frontal lobes.
异染性脑白质营养不良(MLD)是一种由于芳基硫酸酯酶 A 缺乏导致的遗传性溶酶体疾病,伴有进行性脱髓鞘和神经功能下降。本回顾性 MRI 研究旨在探讨诊断时皮质受累的程度,以及与脑受累的常规和区域性容积测量相关的临床相关性。
使用 3D-T1 加权 MRI 扫描来确定皮质厚度以及基于表面的大脑皮质灰质(GM)和大脑白质(WM)体积(GMV 和 WMV)、WM 病变、丘脑和小脑。从 FLAIR 图像中获得 MRI-MLD 严重程度评分。使用相关系数检查临床和影像学数据之间的关联。
纳入 20 例 MLD 患者(平均年龄 13.7 岁,范围 2-35 岁)和 20 名对照者(平均年龄 13.9 岁,范围 2-40 岁)。与对照组相比,晚婴型和少年型患者(n=14)的大脑皮质 GMV 和丘脑体积明显减少(P<0.05),但 WM 和皮质厚度无差异。成年患者(n=6)的 GMV、WMV 和皮质厚度明显减少(均 P<0.05)。区域分析显示 MLD 患者的扣带回皮质和额皮质有统计学上显著的皮质变薄,且随年龄增长变薄趋势更明显。智商(IQ)与 MRI-MLD 评分呈负相关(r=-0.87,P<0.001)。
在 MLD 的早期阶段就已经出现明显的大脑皮质 GMV 丢失。IQ 与 WM 严重程度评分和病变体积相关,但与容积测量无关。在成年患者中,GMV 和 WMV 丢失导致更明显的全脑萎缩,以及更明显的皮质变薄,最明显的是在扣带回和额皮质。