Behavioural and Clinical Neuroscience Institute (BCNI), Department of Psychology, University of Cambridge, Cambridge, UK.
Massachusetts Institute of Technology, Massachusetts General Hospital, and Harvard Medical School, USA.
Neuroimage Clin. 2021;30:102605. doi: 10.1016/j.nicl.2021.102605. Epub 2021 Mar 4.
Recent findings challenge the prior notion that the cerebellum remains unaffected by Alzheimer's disease (AD). Yet, it is unclear whether AD exacerbates age-related cerebellar grey matter decline or engages distinct structural and functional territories. We performed a meta-analysis of cerebellar grey matter loss in normal ageing and AD. We mapped voxels with structural decline onto established brain networks, functional parcellations, and along gradients that govern the functional organisation of the cerebellum. Importantly, these gradients track continuous changes in cerebellar specialisation providing a more nuanced measure of the functional profile of regions vulnerable to ageing and AD. Gradient 1 progresses from motor to cognitive territories; Gradient 2 isolates attentional processing; Gradient 3 captures lateralisation differences in cognitive functions. We identified bilateral and right-lateralised posterior cerebellar atrophy in ageing and AD, respectively. Age- and AD-related structural decline only showed partial spatial overlap in right lobule VI/Crus I. Despite the seemingly distinct patterns of AD- and age-related atrophy, the functional profiles of these regions were similar. Both participate in the same macroscale networks (default mode, frontoparietal, attention), support executive functions and language processing, and did not exhibit a difference in relative positions along Gradients 1 or 2. However, Gradient 3 values were significantly different in ageing vs. AD, suggesting that the roles of left and right atrophied cerebellar regions exhibit subtle functional differences despite their membership in similar macroscale networks. These findings provide an unprecedented characterisation of structural and functional differences and similarities in cerebellar grey matter loss between normal ageing and AD.
最近的发现挑战了先前的观点,即小脑不受阿尔茨海默病(AD)的影响。然而,目前尚不清楚 AD 是否会加剧与年龄相关的小脑灰质减少,还是会涉及到不同的结构和功能区域。我们对正常衰老和 AD 中的小脑灰质丢失进行了荟萃分析。我们将结构下降的体素映射到已建立的大脑网络、功能分区以及控制小脑功能组织的梯度上。重要的是,这些梯度追踪了小脑专业化的连续变化,为易受衰老和 AD 影响的区域的功能特征提供了更细致的衡量标准。梯度 1 从运动到认知区域;梯度 2 分离注意力处理;梯度 3 捕获认知功能的侧化差异。我们在衰老和 AD 中分别确定了双侧和右侧小脑后部萎缩。与年龄相关和 AD 相关的结构下降仅在右侧小叶 VI/ Crus I 中存在部分空间重叠。尽管 AD 和年龄相关萎缩的模式似乎不同,但这些区域的功能特征相似。两者都参与相同的宏观网络(默认模式、额顶叶、注意力),支持执行功能和语言处理,并且在梯度 1 或 2 上的相对位置没有差异。然而,在衰老与 AD 相比,梯度 3 的值存在显著差异,这表明尽管左、右萎缩的小脑区域都属于相似的宏观网络,但它们的作用存在细微的功能差异。这些发现为正常衰老和 AD 之间小脑灰质丢失的结构和功能差异和相似性提供了前所未有的描述。