Training in lifespan behavioral, social, and neuroscience research connecting early-life cognitive decline to late-life ADRD
Training in lifespan behavioral, social, and neuroscience research connecting early-life cognitive decline to late-life ADRD
批准号:
10652244
负责人:
Maxwell Lorenz Elliott
金额:
$7.31万
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
项目状态:
未结题
起止时间:
2020-09-01 至 2026-08-31
关键词:
AddressAgeAgingAlzheimer&aposs disease pathologyAlzheimer&aposs disease related dementiaAlzheimer&aposs disease riskAmyloidAmyloid beta-ProteinAreaAwardBehavioralBiologicalBiological AgingBiological MarkersBirthBrainCaringChildChildhoodCognitiveCognitive agingComplementDataDeteriorationDiseaseDisease ProgressionEarly InterventionEffectiveness of InterventionsElderlyEnsureEtiologyExposure toGasolineGeroscienceGoalsHealthImpaired cognitionIndividualIndividual DifferencesInterventionLeadLifeLinkLongevityMagnetic Resonance ImagingMeasuresNerve DegenerationNeurobehavioral ManifestationsNeurodegenerative DisordersNeurosciencesNeurosciences ResearchNeurotoxinsNew ZealandOnset of illnessOrganPathologyPhasePhenotypePopulationPreventionPrevention ResearchProliferatingResearchResearch Project GrantsResearch TrainingRiskRisk FactorsSamplingStatistical MethodsSurfaceSurrogate MarkersTechniquesTestingThinnessTrainingWhite Matter HyperintensityWorkage relatedaging brainaging populationarchive dataarchived databiobankcohortdementia riskdisabilityeffectiveness testingevidence basefunctional disabilityhealthy agingin vivoindexinginsightlead exposuremembermiddle ageneuroimagingnovelpreventsocial neurosciencetau Proteinstheories
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Alzheimer’s disease and related dementias (ADRD) represent a growing health concern as the global population ages. While many promising treatments for ADRD have been developed and tested, they have largely failed to prevent disease onset or slow disease progression in older adults. However, research has found that subtle signs of ADRD pathology are detectable decades before disease onset. To develop treatments that can slow the progression of ADRD before intractable deterioration of the brain has taken place, we will need to better understand the lifespan trajectory of cognitive, biological and brain aging and develop biomarkers that can connect subtle signs of individual differences in midlife aging to ADRD in late life. In the F99 phase of the proposed research, the candidate will characterize signatures of midlife brain aging and investigate potential surrogate biomarkers using a multi-faceted approach in the Dunedin Study, a population representative birth cohort now in midlife. Specifically, the candidate will investigate the ability of widely used measures of risk for ADRD in older adults, including white matter hyperintensities and brain age, to measure accelerated cognitive and biological aging in midlife. The candidate will then develop a longitudinal measure from 20 years of biological aging across 19 biomarkers to investigate the consequences of accelerated pace of biological aging on individual differences in the structural integrity of the brain in midlife. Then the candidate will use childhood exposure to the neurotoxin lead, a known risk factor for ADRD, to further examine the utility of these candidate surrogate biomarkers to capture risk-related features of midlife brain aging. In the K00 phase of the proposed research, the candidate will utilize statistical techniques, developed when creating the pace of biological aging in midlife, to measure correlated decline in brain biomarkers in healthy aging and ADRD in older adults. The proposed research will yield techniques to measure accelerated biological aging in midlife and in older adults, as well as insights into ADRD through application of these measures. Critically, the proposed project will provide a deeper understanding of connections between midlife and late life accelerated aging that will contribute to growing efforts to target ADRD intervention earlier in life.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Training in lifespan behavioral, social, and neuroscience research connecting early-life cognitive decline to late-life ADRD
-
批准号:10045355
-
项目类别:
-
资助金额:$3.65万
-
财政年份:2020
-
负责人:Maxwell Lorenz Elliott
-
依托单位:
Training in lifespan behavioral, social, and neuroscience research connecting early-life cognitive decline to late-life ADRD
-
批准号:10250397
-
项目类别:
-
资助金额:$3.57万
-
财政年份:2020
-
负责人:Maxwell Lorenz Elliott
-
依托单位:
Training in lifespan behavioral, social, and neuroscience research connecting early-life cognitive decline to late-life ADRD
-
批准号:10687239
-
项目类别:
-
资助金额:$7.75万
-
财政年份:2020
-
负责人:Maxwell Lorenz Elliott
-
依托单位:
国内基金
海外基金
登录
查看更多内容
补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
-
批准号:JCZRLH202601523
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:
-
依托单位:
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
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:
-
依托单位:
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
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:雷芬芳
-
依托单位:
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:--
-
项目类别:面上项目
-
资助金额:--
-
批准年份:2024
-
负责人:万荣
-
依托单位:
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
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2023
-
负责人:贺志明
-
依托单位:
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:--
-
项目类别:地区科学基金项目
-
资助金额:33万元
-
批准年份:2022
-
负责人:都义日
-
依托单位:
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:--
-
项目类别:面上项目
-
资助金额:52万元
-
批准年份:2022
-
负责人:叶宝东
-
依托单位:
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:
-
项目类别:省市级项目
-
资助金额:10.0万元
-
批准年份:2022
-
负责人:于海兵
-
依托单位:
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
-
项目类别:面上项目
-
资助金额:55.0万元
-
批准年份:2019
-
负责人:辛贵忠
-
依托单位:
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
-
项目类别:青年科学基金项目
-
资助金额:18.0万元
-
批准年份:2016
-
负责人:刘括
-
依托单位: