Understanding the link between sociocultural and biological factors to brain health across race & ethnicity in midlife
了解社会文化和生物因素与跨种族大脑健康之间的联系
基本信息
- 批准号:10429375
- 负责人:
- 金额:$ 13.07万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-06-01 至 2024-05-31
- 项目状态:已结题
- 来源:
- 关键词:AdultAgeAgingAlzheimer disease preventionAlzheimer&aposs disease related dementiaAlzheimer&aposs disease riskAmericanBiologicalBiological AgingBiological AssayBiological FactorsBiological MarkersBlack PopulationsBlack raceBloodCerebrovascular DisordersCerebrovascular systemChildhoodChronologyCognitive agingCommunitiesDNA MethylationDataDiscriminationDisease MarkerEducationElderlyEpigenetic ProcessEthnic OriginEthnic groupExposure toFoundationsFutureGenderGoalsHealthHippocampus (Brain)InfarctionInterventionInterviewLatinxLatinx populationLinkLongitudinal StudiesMagnetic Resonance ImagingMeasuresMediatingMentorsModalityModelingMonitorNerve DegenerationOccupationsParentsParticipantPathologyPathway interactionsPatternProcessRaceResearchResearch TrainingRestSocioeconomic StatusSourceStatistical Data InterpretationStressStructural RacismSystemTestingThickTimeTrainingWeatherWhite Matter Hyperintensityaging brainaging populationbaseblack womenbrain healthbrain magnetic resonance imagingcareercognitive neurosciencecohortcritical perioddesigndisparity reductionethnic diversityexperiencefamily structurehealth inequalitiesknowledge basemagnetic resonance imaging biomarkermethylation biomarkermiddle agenoveloffspringprematureracial and ethnicracial and ethnic disparitiesracial disparityracial diversitysexsocialsocial culturesocial disadvantagestressortheories
项目摘要
PROJECT SUMMARY/ABSTRACT
Black and Latinx in the U.S. experience greater brain aging and increased risk for Alzheimer’s disease and
related dementias (ADRD) than Whites. The weathering hypothesis, originally proposed to explain the premature
decline of health experienced by Black women exposed to stress, social disadvantage, structural racism, and
discrimination, may help explain the faster brain aging and racial/ethnic disparities in ADRD in late life among
older Black and Latinx people. Identifying potential targets for interventions to reduce disparities in brain health
in the diverse aging population is of critical importance to the rapidly expanding aging population. Biological
aging, the progressive loss of system integrity that occurs as we age is proposed as a modifiable process
mediating this health inequality. Further, previous studies show that ADRD pathology begins as early as midlife,
thus, it is critical to evaluate these relationships in midlife, a time that may be the most critical period for
intervention. This proposal leverages data collected from the Offspring Study of Mechanisms for Racial
Disparities in ADRD—a longitudinal study of racially/ethnically diverse middle-aged adults with MRI, blood
assays, and interview data. The primary goals of this K99/R00 proposal are to determine the relationship
between advanced biological aging and MRI biomarkers in racially/ethnically diverse middle-aged adults and to
characterize the links between lifecourse socioeconomic status (SES), advanced biological aging, and MRI
biomarkers of aging and ADRD.
This K99/R00 proposal lays the foundation for an independent research career focused on understanding the
causal pathways linking environmental, sociocultural, and biological factors to disparities in brain health across
race/ethnicity. Together, the research and training plans will allow the applicant to (1) develop expertise in using
multiple modalities to understand biological and brain aging; 2) master causal inference modeling, with special
emphasis on multigroup analyses that compare relationships by race/ethnicity; 3) broaden knowledge base of
health-defining sociocultural factors in midlife; and 4) establish a strong foundation in theory and research related
to cultural influences on brain health. These experiences will supplement the applicant’s strong existing
background in cognitive neuroscience and cognitive aging. Results from this study may point to new sources of
racial/ethnic disparities in brain aging and ADRD that could be future targets for intervention, and help to validate
accessible, blood-based targets for monitoring or prevention of ADRD among diverse communities of middle-
aged adults.
项目总结/文摘
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 }}
Indira Turney其他文献
Indira Turney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('Indira Turney', 18)}}的其他基金
Understanding the link between sociocultural and biological factors to brain health across race & ethnicity in midlife
了解社会文化和生物因素与跨种族大脑健康之间的联系
- 批准号:
10627936 - 财政年份:2022
- 资助金额:
$ 13.07万 - 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: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:
$ 13.07万 - 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:
$ 13.07万 - 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:
$ 13.07万 - 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:
$ 13.07万 - 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:
$ 13.07万 - 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:
$ 13.07万 - 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:
$ 13.07万 - 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:
$ 13.07万 - 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:
$ 13.07万 - 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:
$ 13.07万 - 项目类别:
Operating Grants