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Population neuroscience of sex differences in the Alzheimer's disease biomarker cascade: The role of cerebral small vessel disease

Population neuroscience of sex differences in the Alzheimer's disease biomarker cascade: The role of cerebral small vessel disease
阿尔茨海默病生物标志物级联中性别差异的群体神经科学:脑小血管疾病的作用
批准号:
10595545
负责人:
C. Elizabeth Shaaban
金额:
$12.57万
依托单位国家:
美国
项目类别:
财政年份:
2022
资助国家:
美国
项目状态:
未结题
起止时间:
2022-04-01 至 2027-03-31

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中文摘要
翻译
摘要 这项拟议的导师研究科学家职业发展奖(K01)的目的是 支持候选人的长期职业目标,即领导一个研究项目来阐明特定性别 血管对AD和相关痴呆的贡献(ADRD)通过应用最先进的评估- 脑血管完整性的标准和先进的流行病学方法。是否有性行为不同- 脑小血管病(CSVD)至阿尔茨海默病(AD)的病理生理学研究进展 卡德目前还不为人所知。这项提议的第一个目标是测试基于组织的性别差异 CSVD标志物、Aβ、tau和cSVD-AD途径。第二个目标是评估船只的作用- 基于cSVD标记物,通过超高场磁共振测量,在AD级联中,以及是否存在性行为- 相关差异。成功实现应聘者的职业发展目标和研究 目标,建议的K01奖建立在候选人在人口神经科学方面的培训基础上 老年人的衰老和超高场小血管成像的最新方法 除了职业发展和领导力发展外,新培训的四个关键领域:1)队列协调- 方法:2)因果推理方法,以解决高度精选的研究样本的外部有效性; 3)AD病理的PET神经成像;4)性别和性别对AD患者脑病理生理的影响 广告。这项建议包含了几项创新,将使候选人能够更好地评估 在一般人群中,cSVD对于AD生物标记物级联中的性别差异的重要性:1) 应用最先进的超高场MRI获得早期cSVD的直接血管测量和 2)使用创新的神经成像协调和因果推理分析方法来过度 走出“第22条军规”的障碍:典型的神经影像生物标记物研究的外部变量不高。 但在具有人口代表性的大型队列中收集神经成像通常是不可行的。 该应用在指导AD研究的当前理论框架方面也是创新的, 现有不包括脑血管的动态AD生物标志物模型的检验界限 生物标志物。实现这些培训和研究目标将有助于候选人的发展 作为一名独立的调查者和AD特定性别轨迹的领导者。最终,坎迪- Date的更广泛的职业目标是开发一个有影响力的研究计划,确定具体的性别 干预的目标是并改善老年男女的生活。
英文摘要
ABSTRACT The purpose of this proposed Mentored Research Scientist Career Development (K01) Award is to support the Candidate’s long-term career goal of leading a research program to elucidate sex-specific vascular contributions to AD and related dementias (ADRD) by applying the most cutting-edge assess- ments of cerebrovascular integrity and advanced epidemiologic methods. Whether there are sex differ- ences in the cerebral small vessel disease (cSVD)-to-Alzheimer’s disease (AD) pathophysiological cas- cade is currently unknown. The first aim of this proposal is to test for sex differences in tissue-based cSVD markers, Aβ, tau, and the cSVD-AD pathway. The second aim is to evaluate the role of vessel- based cSVD markers, measured by ultra-high field MRI, in the AD cascade and whether there are sex- related differences. To successfully achieve the Candidate’s career development goals and research objectives, the proposed K01 Award builds upon the Candidate's training in population neuroscience of aging and state of the art methods of ultra-high field small vessel imaging in older adults and adds four key areas of new training in addition to career and leadership development: 1) cohort harmoniza- tion methods; 2) causal inference methods to address external validity of highly selected study samples; 3) PET neuroimaging of AD pathology; and 4) sex and gender effects on cerebral pathophysiology of AD. This proposal incorporates several innovations that will allow the Candidate to better assess the importance of cSVD for sex differences in the AD biomarker cascade in the population at large: 1) application of state-of-the-art ultra-high field MRI to obtain direct vessel measures of early cSVD and 2) use of innovative neuroimaging harmonization and causal inference analytic approaches to over- come the “catch 22” obstacle that typical neuroimaging biomarker studies are not high in external va- lidity, but collecting neuroimaging in large, population representative cohorts is typically not feasible. The application is also innovative in relation to the current theoretical framework guiding AD research, testing boundaries of the extant dynamic AD biomarker model which does not include cerebrovascular biomarkers. Achieving these training and research objectives will support the Candidate's development as an independent investigator and a leader in sex-specific trajectories of AD. Ultimately, the Candi- date’s broader career goal is to develop an impactful research program which identifies sex-specific intervention targets and improves the lives of older men and women.
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Population neuroscience of sex differences in the Alzheimer's disease biomarker cascade: The role of cerebral small vessel disease
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