Relationships between local and global mechanisms of sleep apnea, Alzheimer's disease biomarkers, and memory impairment in cognitively asymptomatic older adults

无认知症状老年人睡眠呼吸暂停、阿尔茨海默病生物标志物和记忆障碍的局部和整体机制之间的关系

• 批准号: 10224774
• 负责人: BRYCE A. MANDER
• 金额: $ 12.73万
• 依托单位: UNIVERSITY OF CALIFORNIA-IRVINE
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-08-01 至 2025-04-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10224774
• 关键词: Acoustic Stimulation; Address; Age; Age-associated memory impairment; Aging; Alzheimer' s Disease; Alzheimer' s disease pathology; Alzheimer' s disease related dementia; Alzheimer' s disease risk; Alzheimer’s disease biomarker; Amyloid; Amyloid beta-Protein; Apnea; Atrophic; Biological Markers; Brain; Breathing; Clinical; Clinical Research; Clinical Trials; Clinical Trials Design; Cognitive; Dementia; Development; Differential Diagnosis; Disease Progression; Elderly; Electroencephalography; Epidemiology; Episodic memory; Functional disorder; Funding; Future; Geriatric Psychiatry; Goals; Hippocampus (Brain); Human; Hypoxemia; Impaired cognition; Intervention; Intervention Studies; Knowledge; Link; Magnetic Resonance Imaging; Magnetism; Measures; Medial; Memory; Memory Loss; Memory impairment; Mentors; Methodology; Methods; Molecular; Monitor; Motor Skills; Nerve Degeneration; Neurodegenerative Disorders; Obstructive Sleep Apnea; Onset of illness; Parietal; Pathogenesis; Pathologic; Pathology; Pathway interactions; Patients; Pattern; Perforant Pathway; Pharmacology; Physiological; Play; Population; Positron-Emission Tomography; Postdoctoral Fellow; Prevalence; Preventive treatment; Process; Research; Research Activity; Research Personnel; Research Proposals; Research Training; Resolution; Resources; Risk; Role; Severities; Sleep; Sleep Apnea Syndromes; Sleep Deprivation; Sleep Disorders; Sleep Fragmentations; Sleep disturbances; Slow-Wave Sleep; Structure; Temporal Lobe; Training; Treatment Efficacy; Work; age related; base; career; certificate program; clinically relevant; density; entorhinal cortex; epidemiology study; indexing; memory consolidation; memory encoding; neuroimaging; novel; pre-clinical; pressure; procedural memory; programs; sleep spindle; standard of care; symptomatology; tau Proteins; β-amyloid burden

Project Summary/Abstract Epidemiologic evidence has established obstructive sleep apnea (OSA) as a risk factor for Alzheimer’s disease (AD). However, the mechanisms of this increase in AD risk remain unclear. Three potentially AD-relevant clinical features of OSA include severity of hypoxemia, global sleep fragmentation, and local deficits in memory-relevant sleep oscillations, i.e. slow waves and sleep spindles. These clinical features of OSA have been independently linked to amyloid and tau burden and accumulation, medial temporal lobe (MTL) degeneration, and MTL- dependent memory impairment—all hallmark biomarkers of AD. However, it remains unclear how each of these features relate to AD pathophysiology or MTL-dependent memory decline in patients with OSA. The overarching research objective of this proposal is to address these unknowns. The proposed specific aims are to determine whether distinct global and local OSA features are associated with 1) cortical amyloid burden, 2) MTL tau burden, and 3) degeneration of specific MTL brain circuits supporting multiple forms of memory known to depend on sleep and be vulnerable to AD pathophysiology. The proposed aims will be supported by leveraging existing resources, and collecting high density electroencephalography (hdEEG, 256 channels) sleep recordings in cognitively normal older adults (60-85 years) undergoing positron emission tomography (PET) to assess amyloid and tau burden, as well as ultrahigh resolution magnetic resonance imaging (uhr-MRI) of MTL structure. The proposed study will therefore capitalize on an opportunity to examine how OSA relates to AD pathological burden, MTL structure and function, and memory in an unprecedented level of detail and breadth. This is congruent with both my short and long-term career goals. Specifically, I plan to generate research proposals seeking funding to uncover the impact of distinct forms of sleep disturbance on circuit and molecular mechanisms of AD pathogenesis in humans. This will support my efforts to establish a clinical research program evaluating i) the contribution of sleep disturbance to the onset and progression of various forms of neurodegenerative disease across clinical stages, ii) the utility of sleep-based biomarkers to predict dementia onset and aid differential diagnosis between dementias, and iii) the utility of targeted sleep-based interventions to arrest cognitive decline associated with AD and related dementias. This research proposal and my long-term career goals are supported by my training plan overseen by my mentoring team which includes experts in hdEEG, uhr-MRI, MTL-dependent memory circuit function, PET methods in the context of aging and AD—including amyloid and tau PET, clinical aspects of sleep disorders, geriatric psychiatry, and neurodegenerative disease, and clinical trial design and implementation in the context of sleep disorders and AD. The proposed training plan includes structured mentoring on each of these topics and participation in a clinical research certificate program, as well as a course focused on clinical trials in AD. By establishing this research program, I hope to develop sleep-based approaches to reduce risk, delay onset, and slow progression of dementia and age-related cognitive decline.

项目总结/摘要 流行病学证据已经证实阻塞性睡眠呼吸暂停（OSA）是阿尔茨海默病的一个危险因素 （AD）。然而，AD风险增加的机制仍不清楚。3例潜在AD相关临床 OSA的特征包括低氧血症的严重性、整体睡眠片段化和记忆相关的局部缺陷。 睡眠振荡，即慢波和睡眠纺锤波。OSA的这些临床特征已经被独立地 与淀粉样蛋白和tau蛋白负荷和积累、内侧颞叶（MTL）变性和MTL- 依赖性记忆障碍-AD的所有标志性生物标志物。然而，目前还不清楚这些人是如何 这些特征与OSA患者中AD病理生理学或MTL依赖性记忆衰退有关。总体 本提案的研究目标是解决这些未知数。拟议的具体目标是确定 不同的整体和局部OSA特征是否与1）皮质淀粉样蛋白负荷，2）MTL tau负荷， 和3）支持多种形式记忆的特定MTL脑回路的退化，已知这些记忆依赖于 睡眠和易受AD病理生理影响。将通过利用现有的 资源，并收集高密度脑电图（hdEEG，256通道）睡眠记录， 认知正常的老年人（60-85岁）接受正电子发射断层扫描（PET）以评估淀粉样蛋白 和tau负荷，以及MTL结构的高分辨率磁共振成像（uhr-MRI）。的 因此，拟议的研究将利用机会研究阻塞性睡眠呼吸暂停与AD病理学的关系， 负担，MTL结构和功能，以及前所未有的细节和广度的记忆。这是 与我的短期和长期职业目标一致。具体来说，我计划提出研究建议， 寻求资金，以揭示不同形式的睡眠障碍对电路和分子机制的影响 AD的发病机制。这将支持我建立临床研究计划的努力，评估i） 睡眠障碍对各种形式的神经退行性疾病的发作和进展的贡献 ii）基于睡眠的生物标志物在预测痴呆发作和辅助鉴别痴呆中的效用 痴呆症之间的诊断，和iii）有针对性的基于睡眠的干预措施，以阻止认知能力下降的效用 与AD和相关痴呆症有关。我支持这项研究计划和我的长期职业目标 由我的指导团队监督的培训计划，包括hdEEG、uhr-MRI、MTL依赖性 记忆回路功能，PET方法在衰老和AD的背景下-包括淀粉样蛋白和tau PET，临床 睡眠障碍、老年精神病学和神经退行性疾病方面，以及临床试验设计和 在睡眠障碍和AD的背景下实施。拟议的培训计划包括： 指导这些主题中的每一个，并参与临床研究证书计划，以及课程 专注于AD的临床试验通过建立这个研究项目，我希望开发基于睡眠的方法， 降低风险，延迟发病，减缓痴呆症和年龄相关认知能力下降的进展。