A longitudinal investigation of the cerebellum in adulthood: anatomical and network changes, motor function, and cognition

成年期小脑的纵向研究:解剖和网络变化、运动功能和认知

基本信息

  • 批准号:
    10843004
  • 负责人:
  • 金额:
    $ 6.74万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2019
  • 资助国家:
    美国
  • 起止时间:
    2019-09-01 至 2025-05-31
  • 项目状态:
    未结题

项目摘要

Project Summary The rapid aging of the population of the United States presents new challenges to our society and healthcare system. Understanding the factors that contribute to declines in both motor and cognitive performance is crucial for helping older individuals maintain their quality of life and independence. Further, a better understanding of the patterns of normative age-related change is necessary in order to pinpoint diverging trajectories that may be indicative of pathology, particularly as related to Alzheimer’s disease. Understanding sex differences is also of great importance as older women are disproportionately impacted by Alzheimer’s disease, suffer from more falls, and are more frail than older men. While research investigating the cerebral cortex has expanded our understanding of aging, cerebellar contributions have been overlooked. The cerebellum makes up 10% of the total brain volume, includes more than half of all the neurons in the brain, and is an especially good target for intervention via non-invasive brain stimulation. Further, it contributes to both motor and cognitive function, and shows sex differences in volume in older adults, that may be due in part to hormonal changes with menopause and the action of estrogen on the cerebellum. In the limited work investigating the aging cerebellum, its volumetric declines are second only to those of the hippocampus, and animal models suggest that cerebellar senescence begins sooner than in the hippocampus. Thus, including the cerebellum in models of brain and behavioral change represents an innovative way to improve understanding of age-related performance declines, and may in fact do a better job than the cortex alone. Preliminary findings indicate that cerebellar declines may begin during middle age, and that the structure is associated with motor and cognitive performance in cross-sectional investigations of aging. Here, an expert team of cerebellar, aging, and sex difference researchers will recruit a group of 150 healthy adults over the age of 35 (75 males, 75 females) for a 2-year longitudinal study of the cerebellum and behavior in middle age and older adulthood. The objective of this proposal is to quantify regional cerebellar volume, cerebello-thalamo-cortical networks, and motor and cognitive function to investigate cerebellar and behavioral trajectories. Aim 1 will quantify changes over time in cerebellar structure and networks to define these trajectories across adulthood and in aging. Aim 2 is designed to investigate brain-behavior relationships and determine how cerebellar changes relate to motor and cognitive performance declines. Aim 3 will explore sex differences in cerebellar and behavioral trajectories, with a focus on the influence of menopausal hormonal changes. All three aims will include exploratory analyses that will investigate the relative contributions of the cerebellum, the prefrontal cortex, and the hippocampus. The expected results stand to have a significant impact on our understanding of the aging mind and brain and improve our models of brain and behavioral change in adulthood. Investigating cerebellar trajectories will expand our knowledge of healthy aging, and stands to provide new targets of investigation with respect to age-related diseases, including Alzheimer’s.
项目摘要 美国人口的迅速老龄化给我们的社会和医疗保健系统带来了新的挑战。了解导致运动和认知能力下降的因素对于帮助老年人保持生活质量和独立性至关重要。此外,有必要更好地了解与年龄相关的标准化变化的模式,以便查明可能指示病理学的不同轨迹,特别是与阿尔茨海默病相关的轨迹。了解性别差异也非常重要,因为老年女性受到阿尔茨海默病的影响更大,摔倒的次数更多,而且比老年男性更虚弱。虽然对大脑皮层的研究扩大了我们对衰老的理解,但小脑的作用却被忽视了。小脑占总脑体积的10%,包括大脑中一半以上的神经元,是通过非侵入性脑刺激进行干预的特别好的靶点。此外,它对运动和认知功能都有贡献,并在老年人中显示出体积的性别差异,这可能部分是由于更年期荷尔蒙的变化以及雌激素对小脑的作用。在研究老化小脑的有限工作中,它的体积下降仅次于海马体,动物模型表明,小脑衰老开始得比海马体早。因此,将小脑包括在大脑和行为变化的模型中,代表了一种创新的方式,可以改善对与年龄相关的表现下降的理解,而且实际上可能比单独使用大脑皮层做得更好。初步研究结果表明,小脑衰退可能开始于中年,而且在对衰老的横断面研究中,小脑结构与运动和认知表现有关。在这里,一个研究小脑、衰老和性别差异的专家团队将招募150名年龄在35岁以上的健康成年人(75名男性,75名女性),进行为期两年的小脑和中老年行为的纵向研究。这项建议的目的是量化局部小脑体积、小脑-丘脑-皮质网络以及运动和认知功能,以研究小脑和行为轨迹。目标1将量化小脑结构和网络随时间的变化,以确定这些轨迹在成年期和衰老过程中的变化。AIM 2旨在研究大脑-行为关系,并确定小脑变化与运动和认知能力下降的关系。目标3将探索小脑和行为轨迹的性别差异,重点是更年期激素变化的影响。所有这三个目标都将包括探索性分析,调查小脑、前额叶皮质和海马体的相对贡献。预期的结果将对我们对大脑和大脑老化的理解产生重大影响,并改进我们成年后大脑和行为变化的模型。研究小脑轨迹将扩大我们对健康老龄化的了解,并有望为包括阿尔茨海默氏症在内的与年龄相关的疾病提供新的研究目标。

项目成果

期刊论文数量(12)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Don't forget the little brain: A framework for incorporating the cerebellum into the understanding of cognitive aging.
The association of reproductive stage with lobular cerebellar network connectivity across female adulthood.
  • DOI:
    10.1016/j.neurobiolaging.2022.05.014
  • 发表时间:
    2022-09
  • 期刊:
  • 影响因子:
    4.2
  • 作者:
    Ballard, Hannah K.;Jackson, T. Bryan;Hicks, Tracey H.;Bernard, Jessica A.
  • 通讯作者:
    Bernard, Jessica A.
Anodal cerebellar stimulation increases cortical activation: Evidence for cerebellar scaffolding of cortical processing.
  • DOI:
    10.1002/hbm.26166
  • 发表时间:
    2023-03
  • 期刊:
  • 影响因子:
    4.8
  • 作者:
  • 通讯作者:
Cerebellar Dentate Connectivity across Adulthood: A Large-Scale Resting State Functional Connectivity Investigation.
小脑齿状连通性在整个成年期:一项大规模的静止状态功能连接研究。
  • DOI:
    10.1093/texcom/tgab050
  • 发表时间:
    2021
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Bernard JA;Ballard HK;Jackson TB
  • 通讯作者:
    Jackson TB
Shaky scaffolding: Age differences in cerebellar activation revealed through activation likelihood estimation meta-analysis.
  • DOI:
    10.1002/hbm.25191
  • 发表时间:
    2020-12-15
  • 期刊:
  • 影响因子:
    4.8
  • 作者:
    Bernard JA;Nguyen AD;Hausman HK;Maldonado T;Ballard HK;Jackson TB;Eakin SM;Lokshina Y;Goen JRM
  • 通讯作者:
    Goen JRM
{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

Jessica Ann Bernard其他文献

Jessica Ann Bernard的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('Jessica Ann Bernard', 18)}}的其他基金

A longitudinal investigation of the cerebellum in adulthood: anatomical and network changes, motor function, and cognition
成年期小脑的纵向研究:解剖和网络变化、运动功能和认知
  • 批准号:
    10412042
  • 财政年份:
    2019
  • 资助金额:
    $ 6.74万
  • 项目类别:
A longitudinal investigation of the cerebellum in adulthood: anatomical and network changes, motor function, and cognition
成年期小脑的纵向研究:解剖和网络变化、运动功能和认知
  • 批准号:
    10669668
  • 财政年份:
    2019
  • 资助金额:
    $ 6.74万
  • 项目类别:
A longitudinal investigation of the cerebellum in adulthood: anatomical and network changes, motor function, and cognition
成年期小脑的纵向研究:解剖和网络变化、运动功能和认知
  • 批准号:
    10170211
  • 财政年份:
    2019
  • 资助金额:
    $ 6.74万
  • 项目类别:
A longitudinal investigation of the cerebellum in adulthood: anatomical and network changes, motor function, and cognition
成年期小脑的纵向研究:解剖和网络变化、运动功能和认知
  • 批准号:
    10629848
  • 财政年份:
    2019
  • 资助金额:
    $ 6.74万
  • 项目类别:
Cerebellar Contributions to Disease Course in Youth At High-Risk of Psychosis
小脑对精神病高危青少年疾病进程的影响
  • 批准号:
    8646069
  • 财政年份:
    2013
  • 资助金额:
    $ 6.74万
  • 项目类别:
Cerebellar Contributions to Disease Course in Youth At High-Risk of Psychosis
小脑对精神病高危青少年疾病进程的影响
  • 批准号:
    8822140
  • 财政年份:
    2013
  • 资助金额:
    $ 6.74万
  • 项目类别:

相似国自然基金

靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
  • 批准号:
    JCZRQN202500010
  • 批准年份:
    2025
  • 资助金额:
    0.0 万元
  • 项目类别:
    省市级项目
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
  • 批准号:
    2025JJ70209
  • 批准年份:
    2025
  • 资助金额:
    0.0 万元
  • 项目类别:
    省市级项目
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
  • 批准号:
  • 批准年份:
    2024
  • 资助金额:
    0 万元
  • 项目类别:
    面上项目
甜茶抑制AGE-RAGE通路增强突触可塑性改善小鼠抑郁样行为
  • 批准号:
    2023JJ50274
  • 批准年份:
    2023
  • 资助金额:
    0.0 万元
  • 项目类别:
    省市级项目
蒙药额尔敦-乌日勒基础方调控AGE-RAGE信号通路改善术后认知功能障碍研究
  • 批准号:
  • 批准年份:
    2022
  • 资助金额:
    33 万元
  • 项目类别:
    地区科学基金项目
LncRNA GAS5在2型糖尿病动脉粥样硬化中对AGE-RAGE 信号通路上相关基因的调控作用及机制研究
  • 批准号:
    n/a
  • 批准年份:
    2022
  • 资助金额:
    10.0 万元
  • 项目类别:
    省市级项目
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
  • 批准号:
    81973577
  • 批准年份:
    2019
  • 资助金额:
    55.0 万元
  • 项目类别:
    面上项目
AGE/RAGE通路microRNA编码基因多态性与2型糖尿病并发冠心病的关联研究
  • 批准号:
    81602908
  • 批准年份:
    2016
  • 资助金额:
    18.0 万元
  • 项目类别:
    青年科学基金项目
高血糖激活滑膜AGE-RAGE-PKC轴致骨关节炎易感的机制研究
  • 批准号:
    81501928
  • 批准年份:
    2015
  • 资助金额:
    18.0 万元
  • 项目类别:
    青年科学基金项目

相似海外基金

The Phenomenon of Stem Cell Aging according to Methylation Estimates of Age After Hematopoietic Stem Cell Transplantation
根据造血干细胞移植后甲基化年龄估算干细胞衰老现象
  • 批准号:
    23K07844
  • 财政年份:
    2023
  • 资助金额:
    $ 6.74万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Analysis of Age-dependent Functional Changes in Skeletal Muscle CB1 Receptors by an in Vitro Model of Aging-related Muscle Atrophy
通过衰老相关性肌肉萎缩的体外模型分析骨骼肌 CB1 受体的年龄依赖性功能变化
  • 批准号:
    22KJ2960
  • 财政年份:
    2023
  • 资助金额:
    $ 6.74万
  • 项目类别:
    Grant-in-Aid for JSPS Fellows
Joint U.S.-Japan Measures for Aging and Dementia Derived from the Prevention of Age-Related and Noise-induced Hearing Loss
美日针对预防与年龄相关和噪声引起的听力损失而导致的老龄化和痴呆症联合措施
  • 批准号:
    23KK0156
  • 财政年份:
    2023
  • 资助金额:
    $ 6.74万
  • 项目类别:
    Fund for the Promotion of Joint International Research (International Collaborative Research)
The Effects of Muscle Fatigability on Gait Instability in Aging and Age-Related Falls Risk
肌肉疲劳对衰老步态不稳定性和年龄相关跌倒风险的影响
  • 批准号:
    10677409
  • 财政年份:
    2023
  • 资助金额:
    $ 6.74万
  • 项目类别:
Characterizing gut physiology by age, frailty, and sex: assessing the role of the aging gut in "inflamm-aging"
按年龄、虚弱和性别表征肠道生理学特征:评估衰老肠道在“炎症衰老”中的作用
  • 批准号:
    497927
  • 财政年份:
    2023
  • 资助金额:
    $ 6.74万
  • 项目类别:
Deciphering the role of osteopontin in the aging eye and age-related macular degeneration
破译骨桥蛋白在眼睛老化和年龄相关性黄斑变性中的作用
  • 批准号:
    10679287
  • 财政年份:
    2023
  • 资助金额:
    $ 6.74万
  • 项目类别:
Role of AGE/RAGEsignaling as a driver of pathological aging in the brain
AGE/RAGE信号传导作为大脑病理性衰老驱动因素的作用
  • 批准号:
    10836835
  • 财政年份:
    2023
  • 资助金额:
    $ 6.74万
  • 项目类别:
Elucidation of the protein kinase NLK-mediated aging mechanisms and treatment of age-related diseases
阐明蛋白激酶NLK介导的衰老机制及年龄相关疾病的治疗
  • 批准号:
    23K06378
  • 财政年份:
    2023
  • 资助金额:
    $ 6.74万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Underlying mechanisms of age-related changes in ingestive behaviors: From the perspective of the aging brain and deterioration of the gustatory system.
与年龄相关的摄入行为变化的潜在机制:从大脑老化和味觉系统退化的角度来看。
  • 批准号:
    23K10845
  • 财政年份:
    2023
  • 资助金额:
    $ 6.74万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Targeting Age-Activated Proinflammatory Chemokine Signaling by CCL2/11 to Enhance Skeletal Muscle Regeneration in Aging
通过 CCL2/11 靶向年龄激活的促炎趋化因子信号传导以增强衰老过程中的骨骼肌再生
  • 批准号:
    478877
  • 财政年份:
    2023
  • 资助金额:
    $ 6.74万
  • 项目类别:
    Operating Grants
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了