Longitudinal Investigation of Sleep, Memory, and Brain Development Across the Nap Transition
午睡过渡期间睡眠、记忆和大脑发育的纵向研究
基本信息
- 批准号:10659988
- 负责人:
- 金额:$ 123.47万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2023
- 资助国家:美国
- 起止时间:2023-06-01 至 2028-05-31
- 项目状态:未结题
- 来源:
- 关键词:AddressAgeAnatomyAreaBiological MarkersBrainBrain regionChildChildhoodCognitiveDataData SetDevelopmentDiffusionDiscriminationEcological momentary assessmentHealthHippocampusHumanInterventionInvestigationLearningLongitudinal StudiesMagnetic Resonance ImagingMeasuresMediatingMemoryModelingMonitorNappingOutcomeParentsParticipantPatternPerformancePhasePhysiologicalPolysomnographyReportingResearchRiskScienceSleepSleep ArchitectureStructureSynapsesTestingTimeUnited States National Institutes of HealthWorkactigraphyawakebiomarker identificationcognitive developmentdesignearly childhoodevidence baseforgettinginnovationinsightlongitudinal designmemory consolidationmemory processneuralnovelpredictive markerpressurerapid growthrecruitsexsleep physiologysleep regulationtheories
项目摘要
PROJECT SUMMARY
Sleep stabilizes memories in cortical regions and optimizes synaptic organization, freeing up the hippocampus
for ongoing learning. In early childhood, naps serve a critical function, enhancing memory through sleep-
dependent memory consolidation. Given this, it remains unknown why children transition out of naps when they
are still in a stage rich with learning. We predict that critical brain development occurs at this time, making the
mid-day “unloading” of memories no longer essential. Here we propose the first longitudinal study of the
cognitive, physiological, and neural changes that accompany the nap transition. The central hypothesis is that
maturation of the brain (in particular, the hippocampus) during early childhood results in more information being
retained without interference, reducing the need for frequent consolidation that takes place during naps. We posit
that these changes contribute to the biphasic (nap and overnight sleep) to monophasic (overnight sleep) sleep
transition. To examine this, we will recruit 180 participants (36-54 months) and use a longitudinal design to
assess brain development in relation to memory, sleep physiology, and nap status across the nap transition.
Nap status will be monitored in real-time with actigraphy and verified via parent-reported ecological momentary
assessments. Sleep will be assessed with polysomnography during the nap and overnight sleep. Memory will
be assessed with a mnemonic similarity task, designed to tap hippocampal-dependent memory. Assessments
will occur before and after a nap (with an equivalent interval awake as a control) and again before and after
subsequent overnight sleep. Brain macro/micro structure and anatomical/functional connectivity will be
measured with MRI. Aim 1 is to identify neural markers that predict the shift from biphasic to monophasic sleep.
Aim 2 is to examine changes in sleep-dependent memory processing across the sleep transition. Aim 3 is to
examine changes in diurnal and nocturnal sleep microstructure and topography across the sleep transition. Aim
4 is to examine interrelations among sleep architecture, memory, and the brain across the sleep transition using
latent change score modeling. Innovative aspects of the proposed work include: real-time tracking of nap
transitions longitudinally within the same subjects; examination of nap and overnight sleep microstructure and
topography; comprehensive and targeted measures of brain development; measures of hippocampal-mediated
memory; and latent change score modeling. This work will also result in a novel and rich dataset for additional
analyses by our group and others to test alternative outcomes, explore the contribution of additional brain
regions, and assess additional hypotheses from other prominent sleep theories. This work will have significant
implications for human health by enhancing understanding of the mechanisms underlying sleep regulation and
the consequences of sleep on cognitive health and performance and identification of biomarkers in sleep which
may be useful in identifying risk and health outcomes.
项目总结
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
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 }}
TRACY L. RIGGINS其他文献
TRACY L. RIGGINS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('TRACY L. RIGGINS', 18)}}的其他基金
Hippocampal-Memory Network Development and Episodic Memory in Early Childhood
幼儿期海马记忆网络的发展和情景记忆
- 批准号:
9054144 - 财政年份:2014
- 资助金额:
$ 123.47万 - 项目类别:
Neurobehavioral Investigation of Recollection and Familiarity in Early Childhood
幼儿期记忆和熟悉度的神经行为调查
- 批准号:
8030222 - 财政年份:2011
- 资助金额:
$ 123.47万 - 项目类别:
Neurobehavioral Investigation of Recollection and Familiarity in Early Childhood
幼儿期记忆和熟悉度的神经行为调查
- 批准号:
8206470 - 财政年份:2011
- 资助金额:
$ 123.47万 - 项目类别:
Neural Correlates of Risk-Taking in Adolescents Exposed to Drugs Prenatally
产前接触药物的青少年冒险行为的神经相关性
- 批准号:
7869144 - 财政年份:2010
- 资助金额:
$ 123.47万 - 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
补肾健脾祛瘀方调控AGE/RAGE信号通路在再生障碍性贫血骨髓间充质干细胞功能受损的作用与机制研究
- 批准号:
- 批准年份:2022
- 资助金额:52 万元
- 项目类别:面上项目
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:
- 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
Collaborative Research: Resolving the LGM ventilation age conundrum: New radiocarbon records from high sedimentation rate sites in the deep western Pacific
合作研究:解决LGM通风年龄难题:西太平洋深部高沉降率地点的新放射性碳记录
- 批准号:
2341426 - 财政年份:2024
- 资助金额:
$ 123.47万 - 项目类别:
Continuing Grant
Collaborative Research: Resolving the LGM ventilation age conundrum: New radiocarbon records from high sedimentation rate sites in the deep western Pacific
合作研究:解决LGM通风年龄难题:西太平洋深部高沉降率地点的新放射性碳记录
- 批准号:
2341424 - 财政年份:2024
- 资助金额:
$ 123.47万 - 项目类别:
Continuing Grant
PROTEMO: Emotional Dynamics Of Protective Policies In An Age Of Insecurity
PROTEMO:不安全时代保护政策的情绪动态
- 批准号:
10108433 - 财政年份:2024
- 资助金额:
$ 123.47万 - 项目类别:
EU-Funded
The role of dietary and blood proteins in the prevention and development of major age-related diseases
膳食和血液蛋白在预防和发展主要与年龄相关的疾病中的作用
- 批准号:
MR/X032809/1 - 财政年份:2024
- 资助金额:
$ 123.47万 - 项目类别:
Fellowship
Atomic Anxiety in the New Nuclear Age: How Can Arms Control and Disarmament Reduce the Risk of Nuclear War?
新核时代的原子焦虑:军控与裁军如何降低核战争风险?
- 批准号:
MR/X034690/1 - 财政年份:2024
- 资助金额:
$ 123.47万 - 项目类别:
Fellowship
Walkability and health-related quality of life in Age-Friendly Cities (AFCs) across Japan and the Asia-Pacific
日本和亚太地区老年友好城市 (AFC) 的步行适宜性和与健康相关的生活质量
- 批准号:
24K13490 - 财政年份:2024
- 资助金额:
$ 123.47万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Discovering the (R)Evolution of EurAsian Steppe Metallurgy: Social and environmental impact of the Bronze Age steppes metal-driven economy
发现欧亚草原冶金的(R)演变:青铜时代草原金属驱动型经济的社会和环境影响
- 批准号:
EP/Z00022X/1 - 财政年份:2024
- 资助金额:
$ 123.47万 - 项目类别:
Research Grant
ICF: Neutrophils and cellular senescence: A vicious circle promoting age-related disease.
ICF:中性粒细胞和细胞衰老:促进与年龄相关疾病的恶性循环。
- 批准号:
MR/Y003365/1 - 财政年份:2024
- 资助金额:
$ 123.47万 - 项目类别:
Research Grant
Doctoral Dissertation Research: Effects of age of acquisition in emerging sign languages
博士论文研究:新兴手语习得年龄的影响
- 批准号:
2335955 - 财政年份:2024
- 资助金额:
$ 123.47万 - 项目类别:
Standard Grant
Shaping Competition in the Digital Age (SCiDA) - Principles, tools and institutions of digital regulation in the UK, Germany and the EU
塑造数字时代的竞争 (SCiDA) - 英国、德国和欧盟的数字监管原则、工具和机构
- 批准号:
AH/Y007549/1 - 财政年份:2024
- 资助金额:
$ 123.47万 - 项目类别:
Research Grant














{{item.name}}会员




