German Center for Vertigo and Balance Disorders and Department of Neurology, Munich University Hospital, LMU Munich, Marchioninistr. 15, 81377, Munich, Germany.
German Center for Vertigo and Balance Disorders (DSGZ), LMU Munich, Munich, Germany.
J Neurol. 2023 Nov;270(11):5449-5460. doi: 10.1007/s00415-023-11859-z. Epub 2023 Jul 22.
We aimed to relate clinical measures of disability in chronic cerebellar degeneration to structural whole-brain changes using voxel-based and surface-based morphometry (vbm and sbm). We were particularly interested in remote effects of cerebellar degeneration in the cerebral cortex.
We recruited 30 patients with cerebellar degeneration of different aetiologies (downbeat nystagmus syndrome, DBN n = 14, spinocerebellar ataxia, SCA n = 9, sporadic adult late-onset ataxia, SAOA n = 7). All patients were thoroughly characterised in the motor, cognitive, vestibular and ocular-motor domains. Vbm and sbm were used to evaluate structural differences between cerebellar degeneration patients and a group of healthy age- and gender-matched volunteers. Linear regression models were used to correlate functional measures of disease progression and postural stability with whole brain volumetry.
Patients with SCA and SAOA showed widespread volume loss in the cerebellar hemispheres and less prominently in the vermis. Patients with DBN showed a distinct pattern of grey matter volume (GMV) loss that was restricted to the vestibular and ocular-motor representations in lobules IX, X and V-VII. Falls were associated with brainstem white matter volume. VBM and SBM linear regression models revealed associations between severity of ataxic symptoms, cognitive performance and preferred gait velocity. This included extra-cerebellar (sub-)cortical hubs of the motor and locomotion network (putamen, caudate, thalamus, primary motor cortex, prefrontal cortex) and multisensory areas involved in spatial navigation and cognition.
Functional disability in multiple domains was associated with structural changes in the cerebral cortex.
我们旨在使用基于体素和基于表面的形态计量学(vbm 和 sbm)将慢性小脑变性的临床残疾测量与全脑结构变化相关联。我们特别关注小脑变性对大脑皮层的远程影响。
我们招募了 30 名患有不同病因的小脑变性患者(下跳性眼球震颤综合征,DBN n = 14,脊髓小脑性共济失调,SCA n = 9,散发性成人迟发性共济失调,SAOA n = 7)。所有患者均在运动、认知、前庭和眼动领域进行了全面的特征描述。使用 vbm 和 sbm 评估小脑变性患者与一组年龄和性别匹配的健康志愿者之间的结构差异。线性回归模型用于将疾病进展和姿势稳定性的功能测量与全脑容积相关联。
SCA 和 SAOA 患者的小脑半球和蚓部都有广泛的体积损失,而 DBN 患者的灰质体积(GMV)损失则局限于 IX、X 和 V-VII 叶的前庭和眼动代表区。跌倒与脑干白质体积有关。VBM 和 SBM 线性回归模型显示了共济失调症状严重程度、认知表现和首选步态速度之间的关联。这包括运动和运动网络的额外小脑(亚)皮质中枢(壳核、尾状核、丘脑、初级运动皮质、前额叶皮质)和参与空间导航和认知的多感觉区。
多个领域的功能障碍与大脑皮层的结构变化相关。