Neural basis for differential vulnerability to sleep deprivation

睡眠剥夺差异脆弱性的神经基础

• 批准号: 7993423
• 负责人: Hengyi Rao
• 金额: $ 46.25万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-07-02 至 2015-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7993423
• 关键词: Accidents; Adult; Affect; Anterior; Arousal; Attention; Base of the Brain; Behavioral; Biological Markers; Brain; Brain imaging; Brain region; Cardiovascular Diseases; Cerebrovascular Circulation; Cognitive; Cognitive deficits; Collaborations; Core-Binding Factor; Data; Deterioration; Diabetes Mellitus; Dissociation; Etiology; Functional Imaging; Functional Magnetic Resonance Imaging; Hour; Imaging Techniques; Individual; Individual Differences; Inferior; Knowledge; Laboratories; Measurement; Measures; Medial; Mental Depression; Methods; Modeling; Mood Disorders; Neurocognitive; Obesity; Parietal Lobe; Pennsylvania; Performance; Perfusion; Phenotype; Population; Positioning Attribute; Prefrontal Cortex; Prevalence; Psychomotor Performance; Relative (related person); Reproducibility; Research; Research Infrastructure; Research Personnel; Resistance; Rest; Risk Factors; Sampling; Shift-Work Sleep Disorder; Short-Term Memory; Sleep; Sleep Apnea Syndromes; Sleep Deprivation; Sleep Disorders; Sleep Stages; Societies; Spin Labels; Task Performances; Techniques; Testing; Thalamic structure; Theoretical model; Time; Training; Universities; Work; alertness; base; career; cingulate cortex; cognitive change; cost; executive function; experience; indexing; mortality; neurobehavioral; neuroimaging; neuromechanism; prevent; prospective; public health relevance; relating to nervous system; research facility; response; social; trait; vigilance

DESCRIPTION (provided by applicant): Sleep loss increases sleep propensity, destabilizes the wake state, impairs psychomotor and cognitive performance, and causes considerable social, financial and health-related costs. Although insufficient sleep is a risk factor for obesity, cardiovascular disease and diabetes, depression, and prospective mortality, about 20% to 40% of the US adults sleep less than the minimum sleep duration (7-8 hours per night) to prevent cumulative deterioration in cognitive performance. Neurobehavioral evidence from our previous studies and other groups has indicated robust and highly replicable (trait-like) individual differences in the magnitude of sleepiness and cognitive performance vulnerability to sleep deprivation. While some healthy adults show substantial cognitive deficits during sleep loss, others show few cognitive changes when sleep is deprived. However, little is known about why some sleep-deprived people are more prone to cognitive deficits that can result in costly errors and accidents. To answer this question, we propose to combine our interdisciplinary expertise in neuroimaging and neurobehavioral effects of sleep deprivation to elucidate the neural basis underlying this differential cognitive vulnerability. We will use a new technique of arterial spin labeling (ASL) perfusion functional magnetic resonance imaging (fMRI) for quantification of resting brain activity without task and tonic activation during performance of the psychomotor vigilance test (PVT) in a large sample of N=60 healthy subjects after normal sleep and following sleep deprivation. PVT is a simple, reliable and highly sensitive task for measuring attentional and performance deficits due to sleep deprivation. We will also use traditional BOLD fMRI for measuring phasic activation during fast and slow PVT responses and functional connectivity analysis for studying brain connectivity after normal sleep and following sleep deprivation. The findings from this project will elucidate the neural mechanisms by which sleep deprivation affects behavioral performance and how the effects of sleep deprivation vary across individuals of differential vulnerability. The new knowledge gained from this study will have relevance for understanding and managing excessive sleepiness due to a number of common sleep disorders (e.g., sleep apnea and other sleep disorders; affective disorders; shift work sleep disorder). The project also has the potential to yield brain-based biomarkers that can be used to predict individual responses to sleep deprivation and its treatment. PUBLIC HEALTH RELEVANCE: Although insufficient sleep is a risk factor for obesity, cardiovascular disease and diabetes, depression, and prospective mortality, about 20% to 40% of the adult US population sleep less than the minimum sleep duration (7-8 hours per night) to prevent cumulative deterioration in performance on a range of cognitive tasks. There are robust and highly replicable individual differences in the magnitude of sleepiness and cognitive performance vulnerability to sleep deprivation. This project will use multimodal brain imaging techniques to evaluate neural predictors of response to sleep deprivation and identify why some sleep-deprived people are more prone to cognitive deficits that can result in costly errors and accidents.

描述(由申请人提供)：睡眠不足会增加睡眠倾向，破坏清醒状态的稳定，损害精神运动和认知能力，并导致相当大的社会、经济和健康相关成本。虽然睡眠不足是肥胖、心血管疾病、糖尿病、抑郁症和预期死亡的风险因素，但约20%至40%的美国成年人睡眠时间少于最低睡眠时间(每晚7-8小时)，以防止认知能力的累积恶化。来自我们之前的研究和其他小组的神经行为证据表明，在嗜睡程度和认知表现对睡眠剥夺的易感性方面，存在强大且高度可复制的(类似特质的)个体差异。虽然一些健康的成年人在睡眠不足时表现出严重的认知缺陷，但另一些人在睡眠被剥夺时几乎没有表现出认知变化。然而，对于为什么一些睡眠不足的人更容易出现认知缺陷，从而导致代价高昂的错误和事故，人们知之甚少。为了回答这个问题，我们建议结合我们在神经成像和睡眠剥夺的神经行为效应方面的跨学科专业知识来阐明这种不同认知脆弱性背后的神经基础。我们将使用一种新的动脉自旋标记(ASL)灌注功能磁共振成像(FMRI)技术，对N=60名健康受试者在正常睡眠和睡眠剥夺后进行精神运动警戒测试(PVT)时，对静息无任务和紧张性激活的脑活动进行量化。PVT是一种简单、可靠和高度敏感的测试方法，可用于测量因睡眠不足而导致的注意力和表现缺陷。我们还将使用传统的BOLD功能磁共振成像来测量快速和慢速PVT反应中的时相激活，并使用功能连接性分析来研究正常睡眠和睡眠剥夺后的大脑连接性。该项目的发现将阐明睡眠剥夺影响行为表现的神经机制，以及睡眠剥夺的影响如何在不同脆弱程度的个人之间变化。从这项研究中获得的新知识将与理解和管理由一些常见的睡眠障碍(例如，睡眠呼吸暂停和其他睡眠障碍；情感障碍；轮班工作睡眠障碍)引起的过度嗜睡有关。该项目还有可能产生基于大脑的生物标志物，可以用来预测个人对睡眠剥夺及其治疗的反应。 公共卫生相关性：虽然睡眠不足是肥胖、心血管疾病、糖尿病、抑郁症和预期死亡率的风险因素，但约20%至40%的美国成年人口睡眠时间少于最低睡眠时间(每晚7-8小时)，以防止一系列认知任务的表现累积恶化。在嗜睡的程度和认知表现对睡眠剥夺的易感性方面，存在着强大的、高度可复制的个体差异。该项目将使用多模式脑成像技术来评估对睡眠剥夺反应的神经预测因素，并确定为什么一些睡眠不足的人更容易出现认知缺陷，这可能会导致代价高昂的错误和事故。