Sleep as a novel pathway linking chronic psychological stress and inflammation

睡眠是连接慢性心理压力和炎症的新途径

• 批准号: 8517182
• 负责人: Aric Andrew Prather
• 金额: $ 13.8万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-09-01 至 2017-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8517182
• 关键词: Accounting; Address; Affect; Award; Behavior; Behavioral Mechanisms; Biological; C-reactive protein; CD14 gene; Cardiovascular Diseases; Cardiovascular system; Caregiver Burden; Caregivers; Chronic; Chronic stress; Clinical; Complex; Development; Dimensions; Disease; Distress; Economic Burden; Environment; Epidemiology; Foundations; Gene Expression; Genes; Genetic Transcription; Goals; Health; Health behavior; IL6 gene; Immunobiology; Incidence; Individual; Inflammation; Inflammation Mediators; Inflammatory; Interleukin-6; Intervention; K-Series Research Career Programs; Laboratories; Link; Literature; Longitudinal Studies; Measurement; Measures; Mediating; Mentors; Methodology; Molecular; Morbidity - disease rate; NF-kappa B; Pathway interactions; Physiological; Physiology; Population; Prevention; Process; Psychological Stress; Reporting; Research; Research Methodology; Research Training; Risk Factors; Role; Sampling; Scientist; Sleep; Sleep disturbances; Statistical Methods; Stress; TNF gene; Technology; Testing; Time; Training; Tumor Necrosis Factor-alpha; United States; Variant; Woman; Women' s Health; actigraphy; acute stress; biobehavior; cardiovascular disorder risk; cardiovascular risk factor; experience; genome-wide; human TNF protein; immune activation; indexing; inflammatory marker; innovation; maternal stress; monocyte; mortality; novel; novel therapeutics; prospective; research study

DESCRIPTION (provided by applicant): Cardiovascular disease (CVD) is the foremost cause of mortality in the United States, and accounts for over $500 billion per year in economic burden. Chronic stress ranks as one of the leading biobehavioral risk factors for CVD, a relationship that is partially attributable to inflammatory processes elevated during stress. An exciting arena of scientific advancements is focusing on identifying the specific pathways through which chronic stress influences inflammatory activity with emerging evidence to suggest that sleep, which is commonly disrupted during periods of stress, may serve as one key mechanism linking stress and elevated levels of inflammation. It is critical to advance understanding of the interplay between stress and sleep in predicting levels of inflammatory activity because sleep represents a modifiable health behavior. That is, sleep can be targeted for intervention in ways that may ameliorate the deleterious effects of stress on levels of inflammation, and ultimately, CVD risk. This K08 Mentored Clinical Scientist Research Career Development Award seeks to build on my prior training and research to investigate the role of sleep as a pathway linking chronic stress and markers of inflammatory activity relevant to CVD risk. First, this award will provide the opportunity to deepen my understanding of sleep physiology, measurement, and research methodologies, as well as obtain advanced training in longitudinal statistical methods, women's health, and gene expression/immunobiology. Second, as part of an ongoing longitudinal study, I will examine the prospective associations between sleep, measured objectively using actigraphy, and measures of inflammation, including circulating inflammatory mediators (IL-6, TNF-alpha, and CRP) and monocyte expression of targeted inflammatory genes (IL6, TNF, IL1B) in chronically stressed and low stress maternal caregivers followed over 18-months to test whether sleep mediates the stress-inflammation link. This comprehensive training plan and innovative research study will help to elucidate the interdependent relationships between stress and sleep in predicting inflammatory processes key to cardiovascular health. Moreover, findings from this research will lay the foundation for the development and application of novel therapeutic strategies targeting sleep behavior to reduce levels of inflammation among individuals at elevated risk for CVD, particularly those experiencing high levels of stress.

描述（由申请人提供）：心血管疾病（CVD）是美国死亡的首要原因，每年造成超过5000亿美元的经济负担。慢性压力是CVD的主要生物行为风险因素之一，这种关系部分归因于压力期间炎症过程的升高。科学进步的一个令人兴奋的竞技场集中在确定慢性压力影响炎症活动的具体途径上，新出现的证据表明，在压力期间通常被破坏的睡眠可能是连接压力和炎症水平升高的一个关键机制。在预测炎症活动水平方面，推进对压力和睡眠之间相互作用的理解至关重要，因为睡眠代表了一种可改变的健康行为。也就是说，睡眠可以有针对性地进行干预，以减轻压力对炎症水平的有害影响，并最终降低CVD风险。这个K 08指导临床科学家研究职业发展奖旨在建立在我之前的培训和研究的基础上，以调查睡眠作为连接慢性压力和与CVD风险相关的炎症活动标志物的途径的作用。首先，该奖项将提供机会加深我对睡眠生理学，测量和研究方法的理解，并获得纵向统计方法，女性健康和基因表达/免疫生物学的高级培训。第二，作为一项正在进行的纵向研究的一部分，我将研究使用体动记录仪客观测量的睡眠与炎症指标（包括循环炎症介质）之间的前瞻性关联（IL-6、TNF-α和CRP）和靶向炎症基因的单核细胞表达研究人员对长期压力和低压力的母亲照顾者进行了为期18个月的研究，以测试睡眠是否介导了压力-炎症联系。这项全面的培训计划和创新的研究将有助于阐明压力和睡眠之间的相互依赖关系，以预测心血管健康的关键炎症过程。此外，这项研究的发现将为针对睡眠行为的新型治疗策略的开发和应用奠定基础，以降低CVD风险升高的个体的炎症水平，特别是那些经历高水平压力的个体。