Lab of Cognitive Neuroscience, School of Psychology, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
The Multiple Sclerosis Center, 2nd Department of Neurology, AHEPA University Hospital, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
J Integr Neurosci. 2022 Jan 28;21(1):13. doi: 10.31083/j.jin2101013.
The hallmark of Multiple Sclerosis (MS) pathophysiology is the damage to the myelin sheath around axons. The cerebellum is a predilection site for demyelination with a well-recognized role in motor and a rather understudied contribution to cognitive functions. The aim of this study is to investigate patterns of cerebellar grey and white matter pathology, expressed as reduced volume, as well as cortical thickness and their potential contribution to cognitive performance and disability status of patients with MS. 24 patients with MS underwent extensive neuropsychological assessment using paper and pencil tests and the Brain Health Assessment (BHA) tablet-based battery. Cerebellar lobular volumes and thickness were calculated using a volumetric analysis with automated segmentation of the cerebellum and its lobules. The main findings are a reduction of cerebellar grey matter (CGMV) and white matter volumes (CWMV) in lobule X and a widespread cerebellar cortical thinning in patients. Overall disease severity and neurological disability, assessed with the Expanded Disability Status Severity Scale, was correlated with fatigue and information processing speed tasks, but not with CGMV and CWMV. CWMV and CGMV of lobule I-II was negatively correlated with information processing speed, as well as visuospatial memory tests and, finally, inverse cortical thinning associations were noted between the whole cerebellum, lobule I-II, lobule III, lobule VI, Crus I, lobule VIIIA and information processing speed and verbal fluency tasks. The inverse associations observed may represent a compensatory mechanism activated in MS engaging additional high-level cortical areas functionally interconnected with the damaged cerebellum, in order to cope with the cognitive demands of a task.
多发性硬化症(MS)病理生理学的标志是轴突周围髓鞘的损伤。小脑是脱髓鞘的偏爱部位,其在运动功能中具有明显的作用,而在认知功能方面的作用则研究甚少。本研究旨在探讨小脑灰质和白质病理的模式,表现为体积缩小,以及皮质厚度,并探讨其对 MS 患者认知表现和残疾状况的潜在贡献。24 例 MS 患者接受了广泛的神经心理学评估,包括纸笔测试和基于平板电脑的脑健康评估(BHA)测试。使用基于自动分割小脑及其小叶的容积分析来计算小脑小叶的体积和厚度。主要发现是在小叶 X 中出现小脑灰质(CGMV)和白质体积(CWMV)减少,以及广泛的小脑皮质变薄。使用扩展残疾状况量表评估的总体疾病严重程度和神经功能障碍与疲劳和信息处理速度任务相关,但与 CGMV 和 CWMV 无关。小叶 I-II 的 CWMV 和 CGMV 与信息处理速度以及视空间记忆测试呈负相关,最后,整个小脑、小叶 I-II、小叶 III、小叶 VI、Crus I、小叶 VIIIA 与信息处理速度和言语流畅性任务之间存在皮质厚度反相关。观察到的反相关可能代表一种代偿机制,该机制在 MS 中被激活,涉及与受损小脑功能上相互连接的额外高级皮质区域,以应对任务的认知需求。