Air Pollution and Alzheimer's Dementia: Neuropathologic and Olfactory Mechanisms in Multi-Ethnic Longitudinal Cohorts

空气污染和阿尔茨海默氏痴呆：多种族纵向队列的神经病理学和嗅觉机制

• 批准号: 10347348
• 负责人: JAYANT M PINTO
• 金额: $ 74.39万
• 依托单位: BOSTON UNIVERSITY MEDICAL CAMPUS
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-04-15 至 2025-01-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10347348
• 关键词: Affect; Aging; Air; Air Pollutants; Air Pollution; Alzheimer' s Disease; Alzheimer' s disease related dementia; Alzheimer' s disease risk; Anatomy; Animals; Autopsy; Biological Markers; Blood Vessels; Brain; Cerebrovascular Disorders; Clinical; Cognition; Cognitive; Cohort Studies; Collaborations; Data; Deltastab; Dementia; Deposition; Deterioration; Development; Disease; Elderly; Electron Microscopy; Evaluation; Exposure to; Foundations; Geography; Goals; Human; Image; Impaired cognition; Individual Differences; Inflammation; Investigation; Knowledge; Latino; Link; Longitudinal Studies; Longitudinal cohort; Longitudinal cohort study; Measures; Medical; Medical Records; Memory; Metals; Microscopy; Minority; Modeling; Nervous system structure; Neurocognitive; Neurologic; Nitrogen Oxides; Olfactory Pathways; Olfactory dysfunction; Olfactory tract; Outcome; Participant; Particulate Matter; Pathologic; Pathology; Pathway interactions; Physiological; Play; Population; Process; Public Health; Records; Resources; Risk Factors; Role; Smell Perception; Societal Factors; Specimen; Testing; Tissues; Toxic Environmental Substances; base; cerebrovascular; coarse particles; cognitive function; cognitive performance; cohort; dementia risk; disorder risk; multi-ethnic; neuropathology; novel marker; olfactory bulb; pollutant; predictive modeling; public health intervention; religious order study; research study

ABSTRACT Exposure to air pollution may play a role in the development of Alzheimer's disease and related dementias (ADRD), but how it affects neurocognitive aging is largely unknown. Major barriers to understanding include: inadequate assessment of cognitive decline, over-reliance on medical records and claims data to measure dementia status, sparse information on the connection of air pollution exposure to dementia pathology, and poor understanding of underlying mechanisms, including cerebrovascular and olfactory pathways as well as particulate matter (PM) access to the brain. Here, we will remedy these deficiencies by investigating air pollution and ADRD in a setting that: entails regular and systematic longitudinal evaluation of cognitive function and dementia in all participants, postmortem neuropathologic assessments with extensive cerebrovascular detail, and a far-reaching evaluation of the olfactory system, which is uniquely susceptible to airborne insults, as a direct pathway for environmental toxicants to reach the brain and cause ADRD. Covered in this evaluation will be assessments of olfaction, neuropathology of the olfactory bulb, and PM embedded in the olfactory bulb. We take advantage of 5 large, diverse ongoing, harmonized, well-characterized longitudinal cohort studies of neurologic aging that have collected rich clinical information on >4000 older adults: the Memory and Aging Project, the Minority Aging Research Study, the Religious Orders Study, the Latino CORE Study, and the Clinical Core. The data collected include annual assessments of cognition, dementia status, and olfaction, as well as brain specimens at autopsy (N>1600): the Memory and Aging Project, the Minority Aging Research Study, the Religious Orders Study, the Latino CORE Study, and the Clinical Core. We will estimate participants' long-term air pollution exposures using models previously developed by the MESA Air and MESA Coarse projects and use state-of-the-art, advanced microscopy to measure directly PM in the olfactory bulb, a first. We will assess 3 important underlying mechanisms: the olfactory pathway, inflammation (microglial activation), and cerebrovascular disease. Thus, we will be able to determine the effect of air pollution exposure on neurocognitive outcomes, and examine how resultant neuropathology and direct PM deposition explains these relationships. Our goal is to rigorously test the hypothesis that exposure to air pollution impairs cognitive function and accelerates ADRD via PM deposition in the olfactory system resulting in increased AD neuropathology. This project will generate pivotal new information on the contribution of air pollution to ADRD, raising the prospect of reduction of the burden of ADRD on a population scale via public health interventions.

抽象的 暴露于空气污染可能在阿尔茨海默氏病和相关痴呆症的发展中发挥作用 （ADRD），但是它如何影响神经认知衰老是未知的。理解的主要障碍包括： 评估认知能力下降，过度依赖医疗记录和索赔数据以衡量的评估不足 痴呆状态，有关空气污染与痴呆病理学的连接的稀疏信息以及差的信息 了解基本机制，包括脑血管和嗅觉途径以及 颗粒物（PM）进入大脑。在这里，我们将通过调查空气污染来解决这些缺陷 和ADRD在以下环境中：需要对认知功能的规则和系统的纵向评估 所有参与者的痴呆症，死后神经病理学评估，并具有广泛的脑血管细节， 以及对嗅觉系统的深远评估，该系统容易受到空中侮辱的独特感染 环境有毒物质到达大脑并引起ADRD的途径。在此评估中涵盖 评估嗅球的嗅觉，神经病理学以及嵌入嗅球中的PM。 我们利用了5个大型，多样的，持续的，统一的，良好的纵向人群 对> 4000名老年人收集丰富临床信息的神经衰老的研究：记忆和 老化项目，少数族裔老化研究，宗教秩序研究，拉丁裔核心研究和 临床核心。收集的数据包括认知，痴呆状态和嗅觉的年度评估， 以及尸检时的大脑标本（n> 1600）：记忆和老化项目，少数族裔老化研究 研究，宗教秩序研究，拉丁裔核心研究和临床核心。 我们将使用先前由先前开发的模型估算参与者的长期空气污染暴露 Mesa空气和台面粗项目，并使用最先进的高级显微镜直接测量 PM在嗅球中，第一个。我们将评估3种重要的潜在机制：嗅觉途径， 炎症（小胶质激活）和脑血管疾病。因此，我们将能够确定效果 神经认知结果的空气污染暴露，并检查导致的神经病理学和直接PM 沉积解释了这些关系。 我们的目标是严格测试暴露于空气污染的假设会损害认知功能和 通过PM沉积在嗅觉系统中加速ADRD，导致AD神经病理增加。这 项目将产生有关空气污染对ADRD的贡献的关键新信息，从而提高了 通过公共卫生干预措施减轻人口规模的ADRD负担。