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本文引用的文献

1
Anodal cerebellar stimulation increases cortical activation: Evidence for cerebellar scaffolding of cortical processing.阳极小脑刺激增加皮质激活:小脑对皮质处理的支架作用的证据。
Hum Brain Mapp. 2023 Mar;44(4):1666-1682. doi: 10.1002/hbm.26166. Epub 2022 Dec 5.
2
Individualized Functional Subnetworks Connect Human Striatum and Frontal Cortex.个体化功能子网络连接人类纹状体和前额叶皮层。
Cereb Cortex. 2022 Jun 16;32(13):2868-2884. doi: 10.1093/cercor/bhab387.
3
Cerebellar Dentate Connectivity across Adulthood: A Large-Scale Resting State Functional Connectivity Investigation.成年期小脑齿状核连接性:一项大规模静息态功能连接性研究
Cereb Cortex Commun. 2021 Aug 10;2(3):tgab050. doi: 10.1093/texcom/tgab050. eCollection 2021.
4
Differences Changes in Cerebellar Functional Connectivity Between Mild Cognitive Impairment and Alzheimer's Disease: A Seed-Based Approach.轻度认知障碍与阿尔茨海默病之间小脑功能连接的差异变化:基于种子点的方法。
Front Neurol. 2021 Jun 17;12:645171. doi: 10.3389/fneur.2021.645171. eCollection 2021.
5
Functional parcellation of human and macaque striatum reveals human-specific connectivity in the dorsal caudate.人类和猕猴纹状体的功能分区揭示了背侧尾状核中的人类特异性连接。
Neuroimage. 2021 Jul 15;235:118006. doi: 10.1016/j.neuroimage.2021.118006. Epub 2021 Apr 2.
6
"Cerebellar cognitive reserve": a possible further area of investigation.“小脑认知储备”:一个可能的进一步研究领域。
Aging Clin Exp Res. 2021 Oct;33(10):2883-2886. doi: 10.1007/s40520-021-01795-1. Epub 2021 Feb 17.
7
The cerebellum could serve as a potential imaging biomarker of dementia conversion in patients with amyloid-negative amnestic mild cognitive impairment.小脑可能成为淀粉样阴性遗忘型轻度认知障碍患者向痴呆转化的潜在影像生物标志物。
Eur J Neurol. 2021 May;28(5):1520-1527. doi: 10.1111/ene.14770. Epub 2021 Feb 26.
8
Toward a unified analysis of cerebellum maturation and aging across the entire lifespan: A MRI analysis.针对整个生命周期中小脑成熟和衰老的统一分析:一项 MRI 分析。
Hum Brain Mapp. 2021 Apr 1;42(5):1287-1303. doi: 10.1002/hbm.25293. Epub 2021 Jan 1.
9
Shaky scaffolding: Age differences in cerebellar activation revealed through activation likelihood estimation meta-analysis.摇摇欲坠的脚手架:通过激活似然估计荟萃分析揭示的小脑激活中的年龄差异。
Hum Brain Mapp. 2020 Dec 15;41(18):5255-5281. doi: 10.1002/hbm.25191. Epub 2020 Sep 16.
10
Cerebellar and prefrontal-cortical engagement during higher-order rule learning in older adulthood.成年后期高阶规则学习中的小脑和前额叶皮层参与。
Neuropsychologia. 2020 Nov;148:107620. doi: 10.1016/j.neuropsychologia.2020.107620. Epub 2020 Sep 10.

不要忘记小脑袋:将小脑纳入认知老化理解的框架。

Don't forget the little brain: A framework for incorporating the cerebellum into the understanding of cognitive aging.

机构信息

Department of Psychological and Brain Sciences, USA; Texas A&M Institute for Neuroscience, Texas A&M University, USA.

出版信息

Neurosci Biobehav Rev. 2022 Jun;137:104639. doi: 10.1016/j.neubiorev.2022.104639. Epub 2022 Mar 26.

DOI:10.1016/j.neubiorev.2022.104639
PMID:35346747
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9119942/
Abstract

With the rapidly growing population of older adults, an improved understanding of brain and cognitive aging is critical, given the impacts on health, independence, and quality of life. To this point, we have a well-developed literature on the cortical contributions to cognition in advanced age. However, while this work has been foundational for our understanding of brain and behavior in older adults, subcortical contributions, particularly those from the cerebellum, have not been integrated into these models and frameworks. Incorporating the cerebellum into models of cognitive aging is an important step for moving the field forward. There has also been recent interest in this structure in Alzheimer's dementia, indicating that such work may be beneficial to our understanding of neurodegenerative disease. Here, I provide an updated overview of the cerebellum in advanced age and propose that it serves as a critical source of scaffolding or reserve for cortical function. Age-related impacts on cerebellar function further impact cortical processing, perhaps resulting in many of the activation patterns commonly seen in aging.

摘要

随着老年人口的快速增长,鉴于其对健康、独立性和生活质量的影响,我们迫切需要更好地了解大脑和认知老化。在这方面,我们已经有了关于皮质对高龄认知贡献的成熟文献。然而,尽管这项工作是我们理解老年人大脑和行为的基础,但皮质下的贡献,特别是来自小脑的贡献,并没有被纳入这些模型和框架中。将小脑纳入认知老化模型是推动该领域发展的重要一步。最近人们对阿尔茨海默病痴呆症中的这一结构也产生了兴趣,表明这类研究可能有助于我们理解神经退行性疾病。在这里,我提供了关于高龄时小脑的最新概述,并提出它是皮质功能的关键支架或储备源。小脑功能随年龄增长而受到的影响进一步影响皮质处理,这可能导致在衰老过程中常见的许多激活模式。