Bernard Jessica A, Herrejon Ivan A, An Emily, Cina Yamilet, Dabbiru Sameera, Dempsey Jack, Marrie Elise, Medina Michele, Praytor Jessica
Department of Psychological and Brain Sciences Texas A&M University, United States; Texas A&M Institute for Neuroscience Texas A&M University, United States.
Department of Psychological and Brain Sciences Texas A&M University, United States.
Neuroimage Clin. 2025 Mar 17;46:103770. doi: 10.1016/j.nicl.2025.103770.
The past decade has seen an increased interest in the cerebellum, particularly in non-motor behaviors. Emerging work across model systems and in humans has also implicated the cerebellum in Alzheimer's Disease (AD) and in mild cognitive impairment (MCI). While the cerebellum is not seen as being central to the etiology of the disease, it is however recognized as being increasingly important, and most certainly not immune from disease-related pathology and atrophy. In cognitively normal older adults (OA), the cerebellum has been conceptualized as being critical scaffolding for cortical function. This scaffolding may extend to AD and MCI. With respect to functional imaging, this is largely unexplored in AD, as this is a nascent literature. While there are very few studies focused on the cerebellum in AD at this stage, meta-analysis provides a powerful tool for expanding our knowledge of the cerebellum in neurodegenerative disease, and, in turn, for hypothesis generation. We took advantage of activation likelihood estimation (ALE) meta-analysis to investigate overlap in functional activation present in the existing literature. We focused on AD, but also included an exploratory analysis of MCI, based on papers available in our AD search. Our analysis included a total of 29 studies, representing data from 236 individuals with AD, 159 with MCI, and 382 OA. Across these studies, there is no significant overlap in cerebellar activation in AD, though this is present in MCI. Analyses of group differences also suggest that across studies, there are patterns indicative of both greater and reduced activation in AD/MCI relative to OA. Across all findings, overlap was primarily centered on Crus I and Lobule VI. These findings suggest that cerebellar function is negatively impacted in AD, which in turn may impact behavior and symptomatology.
在过去十年中,人们对小脑的兴趣与日俱增,尤其是在非运动行为方面。跨模型系统和人类的新研究还表明,小脑与阿尔茨海默病(AD)和轻度认知障碍(MCI)有关。虽然小脑并非被视为该疾病病因的核心,但它被认为越来越重要,而且肯定无法免受与疾病相关的病理变化和萎缩的影响。在认知正常的老年人(OA)中,小脑被认为是皮质功能的关键支撑结构。这种支撑结构可能延伸至AD和MCI。关于功能成像,这在AD中很大程度上尚未得到探索,因为这是一个新兴的研究领域。虽然目前专注于AD中小脑的研究非常少,但荟萃分析为扩展我们对神经退行性疾病中小脑的认识,进而为提出假设提供了一个强大的工具。我们利用激活可能性估计(ALE)荟萃分析来研究现有文献中存在的功能激活重叠情况。我们专注于AD,但也基于我们在AD搜索中获得的论文对MCI进行了探索性分析。我们的分析总共包括29项研究,代表了来自236名AD患者、159名MCI患者和382名OA的数据。在这些研究中,AD患者的小脑激活没有显著重叠,尽管在MCI中存在这种重叠。组间差异分析还表明,在所有研究中,存在一些模式表明AD/MCI相对于OA的激活既有增强也有减弱。在所有研究结果中,重叠主要集中在小脑 Crus I和小叶VI。这些发现表明,AD患者的小脑功能受到负面影响,这反过来可能会影响行为和症状。