课题基金 / 基金详情

Neurobiological Substrates of SuperAging and the Preservation of Cingulate Cortex

Neurobiological Substrates of SuperAging and the Preservation of Cingulate Cortex
超级衰老的神经生物学底物和扣带皮层的保护
批准号:
8526973
负责人:
Tamar D Gefen
金额:
$2.62万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-06-01 至 2015-05-31

项目摘要

项目成果

Tamar D Gefen的其他基金

相似基金

相关文献

中文摘要
翻译
描述(由申请人提供):80岁以上的美国总人口比例呈指数级上升,从而增加了阿尔茨海默病等痴呆症高危人群的发生率。这项拟议的研究通过研究一组似乎避免了退行性疾病过程的个人来应对这一重大的公共卫生挑战。我们的中心发现了一群独特的“超级老人”,即80岁以上的人,他们表现出优越的记忆功能,并在日常生活中茁壮成长。西北大学的超老研究的目标是确定解剖学、组织病理学、神经心理学、心理社会和遗传因素,这些因素可以解释这些长寿的人认知功能的保留。一种可能的机制可能与抵抗大脑的病理性变化有关,这种变化发生在“正常”衰老和认知能力下降的情况下。有趣的是,在我们的中心,对SuperAger组和对照组的MRI扫描的皮质厚度测量进行的初步分析发现,前扣带回皮质(ACC)的厚度更大。此外,对超老化大脑的初步尸检发现了显著的发现:(1)在ACC中几乎没有斑块和缠结--阿尔茨海默病的特征--以及(2)von Economo神经元(VENS)密度增加,这是高等灵长类ACC的一个独特特征,涉及复杂的推理和高阶认知。这项建议的目的是研究超级老年患者扣带回皮质的结构和病理特征,因为该区域被证明参与促进记忆的执行功能。AIM 1将使用神经成像方法对大量的SuperAger和对照组的扣带回进行详细的感兴趣区域分析,以确定可能代表SuperAging特有的解剖底物的扣带回区域。根据先前的发现,我们假设,与对照组相比,超级老年人在ACC中的扣带回区域的厚度会增加。目的2将使用组织病理学方法来量化死后扣带回的特征,因为它们与年龄有关,包括斑块和缠结的标记以及Vens的计数,来自SuperAger和对照的标本。根据初步发现,与对照组相比,超级老年组扣带回出现病理特征的频率较低,但VEN密度预计在超级老年组最高。将分析目标1中的解剖测量与认知测试中的表现之间的关系,以确定脑-行为关系。还将分析目标2中的组织病理学特征与认知表现之间的关系。这项多学科研究的结果将为老年人保持卓越认知功能的神经机制提供有价值的信息。这个项目是SuperAging研究的一个组成部分,它具有很高的翻译性,因为研究结果将有助于揭示衰老的神经生物学成分,这些成分最终可以指导痴呆症的治疗。神经成像、组织病理学和认知评估方面的高级培训对于实现这些目标至关重要。
英文摘要
DESCRIPTION (provided by applicant): The proportion of the total US population over age 80 is rising exponentially, thus increasing the frequency of those who are at highest risk for developing dementias such as Alzheimer's disease. The proposed research addresses this major public health challenge by studying a population of individuals who seem to avoid degenerative disease processes. Our center identified a unique group of "SuperAgers", individuals over age 80 who demonstrate superior memory functioning and thrive in daily life. The goal of the SuperAging Study at Northwestern University is to identify the anatomic, histopathologic, neuropsychological, psychosocial, and genetic factors that explain preserved cognition in these long-lived persons. One possible mechanism may be linked with resistance to pathologic brain changes that occur with "normal" aging and cognitive decline. Interestingly, at our Center, preliminary analysis of cortical thickness measures from MRI scans of SuperAgers compared to control groups found greater thickness of the anterior cingulate cortex (ACC). Additionally, preliminary post-mortem qualitative examination of SuperAging brains revealed remarkable findings: (1) virtual absence of plaques and tangles-hallmarks of Alzheimer's disease- in the ACC and (2) increased density of von Economo neurons (VENS), a unique feature of the higher primate ACC implicated in complex reasoning and higher-order cognition. The goal of this proposal is to investigate structural and pathologic features of the cingulate cortex in SuperAgers, as this region is shown to mediate executive functions that facilitate memory. Aim 1 will employ a neuroimaging approach to conduct a detailed region-of-interest analysis of the cingulate in large groups of SuperAgers and controls to identify cingulate areas that may represent anatomic substrates unique to SuperAging. Given prior findings, we hypothesize that SuperAgers will have increased thickness in ACC vs. other cingulate regions compared to controls. Aim 2 will employ a histopathologic approach to quantitate features of post-mortem cingulate as they pertain to aging, including markers of plaques and tangles and counts of VENs, in specimens from SuperAgers and controls. Based on preliminary findings, the frequency of pathologic features in the cingulate is expected to be lower in SuperAgers compared to controls~ VEN density, however, is expected to be greatest in SuperAgers. Relationships between anatomic measures in Aim 1 and performance on cognitive tests will be analyzed to identify brain-behavior relationships~ relationships between histopathologic features in Aim 2 and cognitive performance will also be analyzed. Findings from this multidisciplinary study will provide valuable information on neural mechanisms underlying preservation of superior cognitive functioning in old age. The SuperAging Study, of which this project is an integral part, is highly translational as findings will help reveal the neurobiologic constituents f aging that can ultimately guide treatments for dementias. Advanced training in neuroimaging, histopathology, and cognitive assessment are critical for attainment of these goals.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Vulnerability Profiles of Comorbid Alzheimer and TDP-43 Proteinopathies in Amnestic Dementia
Clinical, Neuroanatomic, and Pathologic Signatures of FTLD-tau in Dementia Phenotypes
Clinical, Neuroanatomic, and Pathologic Signatures of FTLD-tau in Dementia Phenotypes
Clinical, Neuroanatomic, and Pathologic Signatures of FTLD-tau in Dementia Phenotypes - Diversity Supplement
海外基金