Inflammation, Stress, and Social Behavior: Using Ecological Assessments and Model

炎症、压力和社会行为：使用生态评估和模型

• 批准号: 8337765
• 负责人: Charles Raison
• 金额: $ 50.56万
• 依托单位: UNIVERSITY OF ARIZONA
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-30 至 2015-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8337765
• 关键词: Ache; Acoustics; Adopted; Affect; Anti-Inflammatory Agents; Anti-inflammatory; Behavior; Behavior assessment; Behavioral; Biological Models; Body Weight decreased; Chronic; Chronic Hepatitis C; Circadian Rhythms; Clinical; Clinical Sciences; Corticotropin; Development; Devices; Disease; Elements; Emotional; Environment; Fatigue; Health; Hepatitis C virus; Home environment; Hour; Human; Hydrocortisone; Immune; Immune response; Impairment; Individual; Inflammation; Inflammatory; Inflammatory Response; Insecta; Institutes; Interferon-alpha; Laboratories; Lead; Link; Loneliness; Measurement; Measures; Mediating; Medical; Mental Depression; Methodology; Modality; Modeling; Morbidity - disease rate; Nature; Nausea; Neurosecretory Systems; Outcome; Pain; Participant; Patient Self-Report; Pattern; Pegylated Interferon Alfa; Personal Satisfaction; Persons; Phenotype; Physiological; Physiological Processes; Physiology; Plasma; Polysomnography; Positioning Attribute; Process; Psychosocial Stress; Quality of life; Randomized; Records; Regimen; Reporting; Research; Ribavirin; Role; Site; Sleep; Slow-Wave Sleep; Social Behavior; Social Environment; Social isolation; Social support; Stimulus; Stress; Symptoms; Testing; Time; Translational Research; Trier Social Stress Test; Tumor Necrosis Factor-alpha; Universities; affiliative behavior; base; biological adaptation to stress; chemokine; cytokine; depressive symptoms; design; health related quality of life; human TNF protein; innovation; insight; interpersonal conflict; mortality; novel; psychosocial; receptor; resilience; response; social; social integration; sound; stressor; therapy development

DESCRIPTION (provided by applicant): Excluding certain insects, humans are the Earth's supremely social species. Befitting this status, it is increasingly clear that social processes are a prime determinant of human health. Whether conceptualized as social integration or social support, positive social connectivity (PSC) has been shown in hundreds of studies to protect against illness development, to reduce morbidity once illness is established and to reduce mortality from an array of natural causes. Conversely, negative social processes (NSP)-whether measured as loneliness, social isolation or interpersonal conflict-predict disease development and concomitant increases in disease-related morbidity and mortality. The current proposal has been designed to identify behavioral and physiological mechanisms through which PCS/NSP interact with psychosocial stress to promote resilience in the context of illness, A central innovation of the current project is that assessments of social processes and stress reactivity will not rely on first person report, on generalizations across a number of circumstances or on retrospective reporting. Rather, PSC/NSP and stress reactivity will be assessed objectively-that is from a third person perspective-in real time and in specific situations. Similarly, rather than relying on the vagaries and complexities of natural disease processes to supply health-relevant behavioral outcomes, we model inflammation (a central element of all disease states) through the use of treatment with interferon (IFN)-alpha, which provides a standardized regimen of chronic cytokine exposure known to produce profound behavioral disturbances, including depression, fatigue and sickness, in a high percentage of individuals. To objectively assess social processes, the current project will employ the Electronically Activated Recorder (EAR), which periodically and unobtrusively records snippets of ambient sounds in people's momentary environments. Participants wear the device while going about their lives. In tracking moment-to-moment ambient sounds, it yields acoustic logs of their behaviors and interactions as they naturally unfold. To objectively assess behavioral and physiological responses to psychosocial stress the current project will employ the Trier Social Stress Test (TSST), a standardized laboratory stressor known to reliably activate behavioral, neuroendocrine and inflammatory responses. These novel methodologies and model systems will be employed to test the hypotheses that (a) pre-existing affiliative and prosocial behavior will promote resilience in the context of chronic inflammation and that (b) -conversely-chronic inflammation will reduce affiliative and prosocial behavior via effects on stress reactivity, neuroendocrine function and sleep. Finally, it will explore (c) the potential mediating role of stress physiology. To test these hypotheses, 120 subjects with chronic hepatitis C virus infection will be randomized to receive treatment with pegylated IFN-alpha plus ribavirin or to postpone treatment for 8 weeks. Prior to randomization and 8 weeks later all subjects will be evaluated with the EAR in their home environments and will undergo TSST, 14 hour diurnal neuroendocrine and immune measurement and overnight sleep polysomnography in the Atlanta Clinical and Translational Science Institute Clinical Interactions Network site at Emory University.

描述（由申请人提供）：除某些昆虫外，人类是地球上最具社会性的物种。与这一地位相称的是，越来越清楚的是，社会进程是人类健康的主要决定因素。无论是将其定义为社会融合还是社会支持，数百项研究都表明，积极的社会联系（PSC）可以预防疾病发展，降低疾病发病率，并降低一系列自然原因造成的死亡率。相反，消极的社会过程（NSP）——无论是以孤独、社会隔离还是人际冲突来衡量——预测疾病的发展和伴随的疾病相关发病率和死亡率的增加。当前的提案旨在确定PCS/NSP与心理社会压力相互作用的行为和生理机制，以促进疾病背景下的恢复力。当前项目的一个核心创新是，对社会过程和压力反应的评估将不依赖于第一人称报告，不依赖于对许多情况的概括或回顾性报告。相反，PSC/NSP和压力反应性将被客观地评估——即从第三人称的角度——在实时和特定的情况下。同样，我们不是依靠自然疾病过程的不可预测性和复杂性来提供与健康相关的行为结果，而是通过使用干扰素(IFN)- α治疗来模拟炎症（所有疾病状态的核心要素），干扰素- α提供了一种慢性细胞因子暴露的标准化方案，已知慢性细胞因子暴露会产生严重的行为障碍，包括抑郁、疲劳和疾病，在很大比例的个体中。为了客观地评估社会过程，目前的项目将使用电子激活记录器（EAR），它会周期性地、不显眼地记录人们瞬间环境中的环境声音片段。参与者在日常生活中佩戴该设备。在实时跟踪环境声音的过程中，它会产生它们自然展开时的行为和相互作用的声学日志。为了客观地评估对心理社会压力的行为和生理反应，目前的项目将采用特里尔社会压力测试（TSST），这是一种标准化的实验室压力源，已知可以可靠地激活行为、神经内分泌和炎症反应。这些新颖的方法和模型系统将被用来检验以下假设：(a)在慢性炎症的背景下，预先存在的亲和亲社会行为将促进恢复力；(b)相反，慢性炎症将通过对应激反应、神经内分泌功能和睡眠的影响来减少亲和亲社会行为。最后，探讨(c)应激生理的潜在调节作用。为了验证这些假设，120名慢性丙型肝炎病毒感染患者将被随机分组，接受聚乙二醇化ifn - α加利巴韦林治疗，或将治疗推迟8周。在随机化之前和8周后，所有受试者将在其家庭环境中使用EAR进行评估，并在埃默里大学亚特兰大临床与转化科学研究所临床相互作用网络网站进行TSST、每天14小时的神经内分泌和免疫测量以及夜间睡眠多导睡眠图检查。