From the Department of Radiology and Tianjin Key Laboratory of Functional Imaging (J.S., N.Z., Q.W., X.Z., W.Q., C.Y.).
Department of Neurology (L.Y., F.-D.S.), Tianjin Medical University General Hospital, Tianjin, China.
AJNR Am J Neuroradiol. 2019 Jul;40(7):1156-1161. doi: 10.3174/ajnr.A6098. Epub 2019 Jun 20.
The cerebellum plays an important role in motor and cognitive functions. However, whether and how the normal-appearing cerebellum is impaired in patients with neuromyelitis optica spectrum disorders remain unknown. We aimed to identify the occult structural damage of the cerebellum in neuromyelitis optica spectrum disorder and its possible causes at the level of substructures.
Normal-appearing gray matter volume of the cerebellar lobules and nuclei and normal-appearing white matter volume of the cerebellar peduncles were compared between patients with neuromyelitis optica spectrum disorder and healthy controls.
The cerebellar damage of patients with neuromyelitis optica spectrum disorder in the hemispheric lobule VI, vermis lobule VI, and all cerebellar nuclei and peduncles was related only to spinal lesions; and cerebellar damage in the hemispheric lobules VIII and X was related only to the aquaporin-4 antibody. The mixed cerebellar damage in the hemispheric lobules V and IX and vermis lobule Crus I was related mainly to spinal lesions; and mixed cerebellar damage in the hemispheric lobule VIIb was related mainly to the aquaporin-4 antibody. Other cerebellar substructures showed no significant cerebellar damage.
We have shown that the damage in cerebellar normal-appearing white matter and normal-appearing gray matter is associated with aquaporin-4-mediated primary damage or axonal degeneration secondary to spinal lesions or both. The etiologic classifications of substructure-specific occult cerebellar damage may facilitate developing neuroimaging markers for assessing the severity and the results of therapy of neuromyelitis optica spectrum disorder occult cerebellar damage.
小脑在运动和认知功能中发挥着重要作用。然而,视神经脊髓炎谱系疾病患者的正常小脑是否以及如何受损尚不清楚。我们旨在确定视神经脊髓炎谱系疾病中小脑的隐匿性结构损伤及其在亚结构水平上的可能原因。
比较视神经脊髓炎谱系疾病患者与健康对照组之间小脑叶和核的正常表现灰质体积以及小脑脚的正常表现白质体积。
视神经脊髓炎谱系疾病患者的小脑半球 VI 叶、蚓部 VI 叶和所有小脑核及脚的损伤仅与脊髓病变有关;小脑半球 VIII 叶和 X 叶的损伤仅与水通道蛋白-4 抗体有关。小脑半球 V 叶和 IX 叶及蚓部 Crus I 的混合性小脑损伤主要与脊髓病变有关;小脑半球 VIIb 的混合性小脑损伤主要与水通道蛋白-4 抗体有关。其他小脑亚结构未显示明显的小脑损伤。
我们已经表明,小脑正常表现白质和正常表现灰质的损伤与水通道蛋白-4 介导的原发性损伤或继发于脊髓病变的轴突变性有关,或两者兼有。亚结构特异性隐匿性小脑损伤的病因分类可能有助于开发神经影像学标志物,以评估视神经脊髓炎谱系疾病隐匿性小脑损伤的严重程度和治疗结果。