The Effects of Cognitive Map Building on the Development of Alzheimer's Disease
认知地图构建对阿尔茨海默病发展的影响
基本信息
- 批准号:10260590
- 负责人:
- 金额:$ 19.13万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2020
- 资助国家:美国
- 起止时间:2020-09-15 至 2024-05-31
- 项目状态:已结题
- 来源:
- 关键词:AdultAlzheimer&aposs DiseaseAlzheimer&aposs disease pathologyAlzheimer&aposs disease patientAlzheimer&aposs disease related dementiaAlzheimer&aposs disease riskAmyloid beta-ProteinAnteriorAttentionAwarenessBehaviorBrainCellsCitiesClinical TrialsCodeCognitionCognitiveCommutingComplexDataData SetDatabasesDependenceDevelopmentDevicesDigit structureDisease ProgressionDisorientationDorsalEnvironmentEtiologyExerciseExhibitsFailureFunctional Magnetic Resonance ImagingFunctional disorderFutureGeographic LocationsGeographyGrainHealth and Retirement StudyHippocampal FormationHippocampus (Brain)HumanImpairmentIndividualInformation RetrievalKnowledgeLeadLightLinkLocationLondonMapsMedialMedical Care CostsMemory LossMotionNavigation SystemNeighborhoodsNerve DegenerationNeurofibrillary TanglesNeuronal PlasticityNeuronsOccupationsOnset of illnessParietal LobeParticipantPathologyPatientsPatternPeriodicityPersonsPolice officerPopulationPositron-Emission TomographyPropertyPsyche structureRattusResearchResourcesRetrievalRoleRouteSignal TransductionStructureSymptomsSystemTechnologyTestingTrainingTravelbasebehavioral studydrug developmententorhinal cortexexperienceexperimental studyfirst respondergray matterhealth datahealthy agingmild cognitive impairmentneuron lossneuropathologypreservationrelating to nervous systemresidenceresponserole modelrural arearural dwellerstau Proteinsway finding
项目摘要
PROJECT SUMMARY
Can regular mental exercises in building cognitive maps delay the onset of Alzheimer’s disease (AD) or
decelerate the progression of AD? The neuropathology of Alzheimer’s disease (AD) begins in the entorhinal
cortex, leading to spatial navigation impairment that differentiates patients with mild cognitive impairment
(MCI) and AD from healthy aging adults. Specifically, MCI and AD patients suffer declining abilities to
allocentric navigation that requires developing a cognitive map (aka mental map) as an internal representation
of the environment with places and features independent of one’s current location or orientation. A system of
spatial cells in the hippocampal formation subserves cognitive map building with the spatial periodicity of grid-
cell firing fields to form the brain’s metric coordinate system for allocentric navigation. Studies showed that
grid cells could gradually lose their spatial periodicity during periods of reduced theta oscillations and
hippocampal inactivation. Will mental exercises in building cognitive maps excite theta oscillations and
hippocampal activation and strengthen spatial periodicity of grid-cell firing fields? Findings of structural brain
changes in London taxi drivers and spatial information retrieval support the potential of such excitatory
effects. Further, less is known about the role of the posterior parietal cortex (PPC) in the storage and retrieval
of cognitive maps, and how this region changes with AD.
The proposed study hypothesizes that regular mental exercises on cognitive map building can evoke
such excitatory effects to delay AD onset and decelerate AD progression. In this exploratory proposal, we
venture into the links amongst geographic environments, allocentric navigation, cognitive maps, and AD
development: a more complex environment imposes a higher demand on cognitive maps to navigate even on
daily commutes and routine errands, and frequent mental exercises of building and retrieving cognitive maps
lead to preservation of spatial cognition relevant gray matter regions and consequently impede AD
development. We will use data from the National Alzheimer’s Coordinating Center (NACC) and US-based
Health and Retirement Study (HRS), respectively (1) to compare MCI/AD populations in geographic areas with
varying degrees of environmental complexity and (2) to investigate MCI/AD populations with occupations of
high dependency on cognitive maps, such as realtors, police officers, first responders, and the other
occupations. The NACC databases contain participant’s 3-digit zip-codes and types of residence which will
allow MCI/AD mapping to potential neighborhoods across the US, whereas HRS restricted data include
occupation data and cross-wave geographic information at street-level. Findings from the exploratory project
will support subsequent experimental research to model the role of gray matter volume, refine the research
framework of the excitatory effects of environment complexity and cognitive mapping to MCI/AD development,
and examine the potential MCI/AD detriments of GPS-enabled navigation devices.
项目总结
建立认知地图的定期心理练习能否延缓阿尔茨海默病(AD)或
减慢AD的进展?阿尔茨海默病(AD)的神经病理学始于内嗅觉
皮质,导致空间导航障碍,区分轻度认知障碍患者
(MCI)和AD。具体地说,MCI和AD患者的能力下降
需要开发认知地图(也称为心理地图)作为内部表征的异地导航
具有与当前位置或方位无关的地点和特征的环境。一种制度
海马结构中的空间细胞以网格的空间周期性来辅助认知地图的构建。
细胞激发区域形成大脑的公制坐标系,用于向外定位导航。研究表明,
网格细胞可能在theta振荡减少和
海马区失活。构建认知地图的心理练习是否会刺激theta振荡和
激活海马区,增强网状细胞射野的空间周期性?结构性脑的表现
伦敦出租车司机的变化和空间信息检索支持了这种兴奋性的潜力
效果。此外,关于后顶叶皮质(PPC)在存储和提取中的作用还知之甚少
认知地图,以及这个区域如何随着AD的变化而变化。
这项拟议的研究假设,有规律的认知地图构建心理练习可以唤起
这种兴奋作用可以延缓AD的发病和减缓AD的进展。在这个探索性的提案中,我们
探索地理环境、地理中心导航、认知地图和AD之间的链接
发展:更复杂的环境对认知地图提出了更高的要求,即使在上面导航
日常通勤和例行公事,以及建立和检索认知地图的频繁脑力练习
导致空间认知相关灰质区域的保存,从而阻碍AD
发展。我们将使用国家阿尔茨海默氏症协调中心(NACC)和美国的数据
健康和退休研究(HRS)分别(1)将地理区域的MCI/AD人群与
不同程度的环境复杂性和(2)调查MCI/AD人群的职业
高度依赖认知地图,如房地产经纪人、警察、急救人员和其他人
职业。NACC数据库包含参与者的3位邮政编码和居住类型,这将
允许将MCI/AD映射到美国各地的潜在社区,而HRS限制的数据包括
街道层面的职业数据和跨波地理信息。探索性项目的发现
将支持后续的实验研究,以模拟灰质体积的作用,完善研究
环境复杂性和认知图谱对MCI/AD发展的兴奋效应框架,
并检查启用GPS的导航设备的潜在MCI/AD危害。
项目成果
期刊论文数量(0)
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Kristen M. Kennedy其他文献
Lifespan longitudinal changes in mesocortical thickness and executive function: Role of dopaminergic genetic predisposition
- DOI:
10.1016/j.neurobiolaging.2024.11.005 - 发表时间:
2025-02-01 - 期刊:
- 影响因子:
- 作者:
Giuseppe G. Miranda;Chen Gonen;Jessica N. Kraft;Karen M. Rodrigue;Kristen M. Kennedy - 通讯作者:
Kristen M. Kennedy
Cortical thickness and low-grade inflammation moderate the association between depressive symptoms and cognitive function in early widowhood: A preliminary study
皮质厚度和低度炎症在早期丧偶中调节抑郁症状与认知功能之间的关联:一项初步研究
- DOI:
10.1016/j.bbi.2025.06.027 - 发表时间:
2025-10-01 - 期刊:
- 影响因子:7.600
- 作者:
E. Lydia Wu-Chung;Kristen M. Kennedy;Luis D. Medina;Paul E. Schulz;Frederick L. Oswald;Cobi J. Heijnen;Stephanie L. Leal;Bryan T. Denny;Christopher P. Fagundes - 通讯作者:
Christopher P. Fagundes
The Dallas Lifespan Brain Study: A Comprehensive Adult Lifespan Data Set of Brain and Cognitive Aging
达拉斯寿命大脑研究:一个全面的成人寿命大脑和认知衰老数据集
- DOI:
10.1038/s41597-025-04847-7 - 发表时间:
2025-05-26 - 期刊:
- 影响因子:6.900
- 作者:
Denise C. Park;Joseph P. Hennessee;Evan T. Smith;Micaela Y. Chan;Xi Chen;Marianna Dakanali;Michelle E. Farrell;Peiying Liu;Hanzhang Lu;Neil Rofsky;Xiankai Sun;Carol Tamminga;William Moore;Kristen M. Kennedy;Karen Rodrigue;Gagan S. Wig - 通讯作者:
Gagan S. Wig
Kristen M. Kennedy的其他文献
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{{ truncateString('Kristen M. Kennedy', 18)}}的其他基金
The Effects of Cognitive Map Building on the Development of Alzheimer's Disease
认知地图构建对阿尔茨海默病发展的影响
- 批准号:
10062274 - 财政年份:2020
- 资助金额:
$ 19.13万 - 项目类别:
Dopaminergic and Neuroplastic Influences on Longitudinal Change in Cognitive and Brain Aging
多巴胺能和神经可塑性对认知和大脑衰老纵向变化的影响
- 批准号:
10162460 - 财政年份:2017
- 资助金额:
$ 19.13万 - 项目类别:
Dopaminergic and Neuroplastic Influences on Longitudinal Change in Cognitive and Brain Aging
多巴胺能和神经可塑性对认知和大脑衰老纵向变化的影响
- 批准号:
9925201 - 财政年份:2017
- 资助金额:
$ 19.13万 - 项目类别:
Role of White Matter Integrity in Age-Related Functional Reorganization
白质完整性在年龄相关功能重组中的作用
- 批准号:
7872547 - 财政年份:2010
- 资助金额:
$ 19.13万 - 项目类别:
Role of White Matter Integrity in Age-Related Functional Reorganization
白质完整性在年龄相关功能重组中的作用
- 批准号:
8723718 - 财政年份:2010
- 资助金额:
$ 19.13万 - 项目类别:
Role of White Matter Integrity in Age-Related Functional Reorganization
白质完整性在年龄相关功能重组中的作用
- 批准号:
8073151 - 财政年份:2010
- 资助金额:
$ 19.13万 - 项目类别:
Role of White Matter Integrity in Age-Related Functional Reorganization
白质完整性在年龄相关功能重组中的作用
- 批准号:
8549045 - 财政年份:2010
- 资助金额:
$ 19.13万 - 项目类别:
Role of White Matter Integrity in Age-Related Functional Reorganization
白质完整性在年龄相关功能重组中的作用
- 批准号:
8540664 - 财政年份:2010
- 资助金额:
$ 19.13万 - 项目类别:














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