Neuroimaging Research Unit, Institute of Experimental Neurology, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy/Vita-Salute San Raffaele University, Milan, Italy.
Neuroimaging Research Unit, Institute of Experimental Neurology, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy/Neurology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Mult Scler. 2021 May;27(6):841-854. doi: 10.1177/1352458520941493. Epub 2020 Jul 16.
The pathogenetic mechanisms sustaining neuroinflammatory disorders may originate from the cerebrospinal fluid.
To evaluate white matter damage with diffusion tensor imaging and T1/T2-weighted ratio at progressive distances from the ventricular system in neuromyelitis optica spectrum disorders and multiple sclerosis.
Fractional anisotropy, mean, axial, and radial diffusivity and T1/T2-weighted ratio maps were obtained from patients with seropositive neuromyelitis optica spectrum disorders, multiple sclerosis, and healthy controls ( = 20 each group). White matter damage was assessed as function of ventricular distance within progressive concentric bands.
Compared to healthy controls, neuromyelitis optica spectrum disorders patients had similar fractional anisotropy, radial and axial diffusivity, increased mean diffusivity ( = 0.009-0.013) and reduced T1/T2-weighted ratio ( = 0.024-0.037) in all bands. In multiple sclerosis, gradient of percentage lesion volume and intra-lesional mean and axial diffusivity were higher in periventricular bands. Compared to healthy controls, multiple sclerosis patients had reduced fractional anisotropy ( = 0.001-0.043) in periventricular bands, increased mean ( < 0.001), radial ( < 0.001-0.004), and axial diffusivity ( = 0.002-0.008) and preserved T1/T2-weighted ratio in all bands.
White matter damage is higher at periventricular level in multiple sclerosis and diffuse in neuromyelitis optica spectrum disorders. Fractional anisotropy preservation, associated with increased mean diffusivity and reduced T1/T2-weighted ratio may reflect astrocyte damage.
维持神经炎症性疾病的发病机制可能源自脑脊液。
评估多发性硬化症和视神经脊髓炎谱系疾病患者脑室系统不同距离处的脑白质弥散张量成像和 T1/T2 加权比值的白质损伤情况。
对血清阳性视神经脊髓炎谱系疾病、多发性硬化症患者和健康对照组(每组 20 例)进行各向异性分数、平均、轴向和径向弥散系数及 T1/T2 加权比值图的检测。根据脑室距离评估白质损伤与进行性同心带的关系。
与健康对照组相比,视神经脊髓炎谱系疾病患者在所有带中均表现出相似的各向异性分数、径向和轴向弥散系数,增加的平均弥散系数(=0.009-0.013)和降低的 T1/T2 加权比值(=0.024-0.037)。多发性硬化症患者在脑室周围带中,病变体积百分比和病灶内平均弥散系数和轴向弥散系数的梯度更高。与健康对照组相比,多发性硬化症患者在脑室周围带中各向异性分数降低(=0.001-0.043),平均弥散系数增加(<0.001),径向弥散系数增加(<0.001-0.004),轴向弥散系数增加(=0.002-0.008),所有带的 T1/T2 加权比值均正常。
多发性硬化症患者的脑室周围水平白质损伤更高,而视神经脊髓炎谱系疾病患者的白质损伤更弥散。各向异性分数保留,同时伴有平均弥散系数增加和 T1/T2 加权比值降低,可能反映了星形胶质细胞损伤。