Mechanisms of Meditation
冥想的机制
基本信息
- 批准号:8470880
- 负责人:
- 金额:$ 5.97万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2009
- 资助国家:美国
- 起止时间:2009-05-01 至 2014-03-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (provided by applicant): The increasingly widespread use of meditation for stress-related emotional and medical conditions highlights the urgent need to rigorously evaluate mechanisms through which the benefits of practice might be conferred. Primary challenges in this regard include evaluating dose response relationships between practice time and outcomes; clarifying whether physiological and behavioral effects of meditation derive primarily from non-specific aspects of training or result from specific meditation practices; and identifying molecular mechanisms by which meditation might affect physiological responses relevant to stress-related illness. Recent findings from a cross-sectional study by our group indicate that young adults who are randomized to, and practice, compassion meditation demonstrate reduced inflammatory responses, less emotional distress, and reduced autonomic responses to a standardized laboratory psychosocial stressor (Trier Social Stress Test [TSST]) when compared to subjects randomized to an active control condition. However, as a result of the cross-sectional study design and lack of a meditation comparator arm, these results provide only partial insight into key issues outlined above regarding the role played by specific meditation procedures and/or practice time in observed physiological and behavioral outcomes. The primary hypothesis of the proposed work is that practicing a meditation procedure specifically designed to enhance empathic concern for others (i.e. compassion meditation) will optimize autonomic reactivity to psychosocial stress in a manner that results in diminished activation of peripheral inflammatory signaling pathways and reduced behavioral distress. To test this hypothesis, the following aims are proposed: Aim 1: to use a longitudinal design to definitively establish that practice time contributes to the effect of compassion meditation on in vivo inflammatory and behavioral responses to psychosocial stress; Aim 2: To examine whether the effect of compassion meditation on behavioral and inflammatory responses to psychosocial stress results specifically from training in the generation of empathic concern for others or derives more generally from learning the basic meditative practices of focused attention and mindfulness; and Aim 3: to investigate autonomic mechanisms by which meditation may attenuate stress-induced inflammation. To accomplish these aims, the current study will randomize 360 medically healthy adults to 6 weeks of either compassion meditation training, Mindful Attention Training (to control for exposure to the basic meditation practices of attention and mindfulness) or a health education discussion group (to control for potential non-specific elements such as group support). Prior to, and upon completion of these interventions, all subjects will undergo TSST testing in order to assess inflammatory, autonomic and behavioral responses to psychosocial stress. Health-relevant behavioral and lifestyle factors will also be assessed to evaluate their contribution to the effect of meditation on inflammation. The long-term health implications of this study will likely be far reaching given evidence that inflammatory pathways represent an important mechanism by which stress promotes and/or worsens many medical and psychiatric conditions. PUBLIC HEALTH RELEVANCE: The increasing use of meditation as a treatment for a variety of stress-related medical conditions highlights the public health importance of identifying mechanisms by which meditation may improve health, both to confirm efficacy for this widely used intervention and to better identify disease states toward which meditation might be optimally applied. The proposed study will test the hypothesis that meditation reduces inflammatory responses to psychosocial stress via reductions in autonomic activation in the face of perceived psychosocial stress. If confirmed, the long-term health implications of this hypothesis would likely be far reaching, given evidence that activation of innate immune inflammatory pathways represents an important mechanism by which stress promotes and/or worsens a wide range of serious medical and psychiatric conditions (i.e. vascular disease, diabetes, cancer, HIV, major depression) to which meditation is being increasingly applied as an intervention.
描述(由申请人提供):冥想越来越广泛地用于与压力有关的情绪和医疗条件,突出了严格评估机制的迫切需要,通过这些机制,实践的好处可能会被赋予。这方面的主要挑战包括评估练习时间和结果之间的剂量反应关系;澄清冥想的生理和行为影响主要来自训练的非特定方面还是来自特定的冥想练习;以及确定冥想可能影响与压力相关疾病相关的生理反应的分子机制。我们小组最近的一项横断面研究结果表明,与随机分配到积极控制条件的受试者相比,随机分配到同情冥想并练习同情冥想的年轻人表现出炎症反应减少,情绪困扰减少,对标准化实验室心理社会压力源(特里尔社会压力测试[TSST])的自主反应减少。然而,由于横截面研究设计和缺乏冥想比较臂,这些结果仅提供了上述关于特定冥想程序和/或练习时间在观察到的生理和行为结果中所起作用的关键问题的部分见解。这项工作的主要假设是,练习一种专门设计用于增强对他人的同理心关注的冥想程序(即同情冥想)将优化对心理社会压力的自主反应,从而减少外周炎症信号通路的激活并减少行为困扰。为了验证这一假设,提出了以下目标:目标1:使用纵向设计来明确地确定练习时间有助于同情冥想对心理社会压力的体内炎症和行为反应的影响;目标2:研究同情冥想对心理社会应激的行为和炎症反应的影响是否特别来自移情产生的训练。关注他人或更普遍地从学习集中注意力和正念的基本冥想实践中获得;目标3:研究冥想可能减弱压力引起的炎症的自主机制。为了实现这些目标,目前的研究将360名医学健康的成年人随机分配到6周的同情冥想训练,正念注意力训练(控制暴露于注意力和正念的基本冥想练习)或健康教育讨论组(控制潜在的非特定元素,如团体支持)。在这些干预之前和完成后,所有受试者将接受TSST测试,以评估对心理社会应激的炎症、自主神经和行为反应。与健康相关的行为和生活方式因素也将被评估,以评估它们对冥想对炎症影响的贡献。这项研究的长期健康影响可能是深远的,因为有证据表明炎症途径是压力促进和/或破坏许多医疗和精神疾病的重要机制。公共卫生关系:越来越多地使用冥想作为各种压力相关疾病的治疗方法,突出了确定冥想可以改善健康的机制的公共卫生重要性,既要确认这种广泛使用的干预措施的有效性,又要更好地确定冥想可能最佳应用的疾病状态。这项拟议中的研究将测试这样一个假设,即冥想通过减少面对感知到的心理社会压力时的自主激活来减少对心理社会压力的炎症反应。如果得到证实,这一假设的长期健康影响可能是深远的,因为有证据表明,先天免疫炎症通路的激活是一种重要的机制,压力可以促进和/或减轻各种严重的医疗和精神疾病(即血管疾病,糖尿病,癌症,艾滋病毒,抑郁症),冥想越来越多地被用作干预措施。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Charles Raison其他文献
Charles Raison的其他文献
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{{ truncateString('Charles Raison', 18)}}的其他基金
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:
8473381 - 财政年份:2011
- 资助金额:
$ 5.97万 - 项目类别:
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 - 财政年份:2011
- 资助金额:
$ 5.97万 - 项目类别:
Neurobiological and Behavioral Effects of Cytokine Antagonism in Major Depression
细胞因子拮抗剂对重度抑郁症的神经生物学和行为影响
- 批准号:
7386120 - 财政年份:2008
- 资助金额:
$ 5.97万 - 项目类别:
Neurobiological and Behavioral Effects of Cytokine Antagonism in Major Depression
细胞因子拮抗剂对重度抑郁症的神经生物学和行为影响
- 批准号:
7546540 - 财政年份:2008
- 资助金额:
$ 5.97万 - 项目类别:
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