Depression, inflammation, and diabetes: Exploring shared etiopathology

抑郁症、炎症和糖尿病：探索共同的病因病理学

• 批准号: 8699522
• 负责人: Briana Mezuk
• 金额: $ 16.99万
• 依托单位: VIRGINIA COMMONWEALTH UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-08-01 至 2016-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8699522
• 关键词: Accounting; Address; Adult; Back; Baltimore; Behavioral; Biological; Biology; Biometry; Cardiovascular Diseases; Cardiovascular system; Catchment Area; Clinical Research; Cohort Studies; Comorbidity; Complex; Data; Development; Development Plans; Diabetes Mellitus; Diet; Elderly; Environmental Exposure; Environmental Risk Factor; Epidemiologic Studies; Epidemiologist; Epidemiology; Foundations; Gene Expression; Gene Expression Alteration; Genes; Genetic; Genetic Research; Genetic Risk; Genomics; Goals; Health; Health Care Costs; Health behavior; Healthcare; Immune; Immunology; Inflammation; Inflammatory; Investigation; K-Series Research Career Programs; Knowledge; Leukocytes; Link; Longevity; Major Depressive Disorder; Mediating; Mediator of activation protein; Medical; Mental Depression; Mental Health; Mental disorders; Mentors; Messenger RNA; Metabolic Diseases; Methods; Modeling; National Health and Nutrition Examination Survey; Nature; Non-Insulin-Dependent Diabetes Mellitus; Pathway interactions; Pattern; Persons; Physiological; Physiology; Prospective Studies; Psychiatry; Psychological Models; Public Health; Recruitment Activity; Registries; Relative (related person); Research; Research Design; Research Personnel; Risk; Risk Factors; Sampling; Smoking; Source; Specific qualifier value; Stress; Technology; Training; Translating; Twin Multiple Birth; Twin Studies; Work; career development; clinical care; cohort; depressive symptoms; design; diabetes risk; flexibility; functional genomics; gene environment interaction; genetic epidemiology; genetic risk factor; glucose metabolism; improved; innovation; mortality; novel; physical conditioning; population based; programs; responsible research conduct; screening

DESCRIPTION (provided by applicant): Epidemiologic and clinical studies have established that Major Depression (MD) often co-occurs with medical conditions in later life, including metabolic disorders such as Type 2 Diabetes Mellitus (hereafter referred to as 'Diabetes'). It is now acknowledged that the inter-relationship between MD and Diabetes is likely bi-directional. Indeed, there is consistent evidence from population-based cohort studies that MD is associated with increased risk of and mortality from Diabetes and cardiovascular disease. However, prospective studies cannot definitively distinguish whether MD is a unique risk factor for metabolic disorders, or if this phenomenon is due to a common factor shared by both MD and Diabetes such as genetic liability, environmental stress, or systemic physiologic deregulation. Functional genomics, particularly assessment of gene expression, offer a novel means of specifying how environmental exposures intersect with genetic liability to influence physiology. The broad objective of this Career Development Award (K01) is to investigate the etiologic relationships between co-occurring MD and Diabetes, in particular the structural and relative contributions of genetic and environmental sources of risk. This research utilizes complementary approaches to investigating the aims below: first, the broad genetic and environmental pathways underlying this comorbidity will be examined using latent variable twin modeling; second, gene expression arrays will be used to examine specific biological pathways by which depressive symptoms influence Diabetes risk. The specific aims of the research plan are to: 1) evaluate environmental and genetic contributions, and their interaction, of the relationship between MD and Diabetes in later adulthood; 2) investigate the behavioral pathways linking MD and Diabetes while accounting for shared genetic liability; and 3) examine the relationship between depressive symptoms and expression of immune-related genes. The candidate will receive training in responsible conduct of research, genetic epidemiology, and functional genomics. The candidate proposes to implement this research plan during a period of closely mentored training with experts in psychiatry, immunology, functional genomics, epidemiology, and biostatistics. The proposed training plan will promote her transition to independence as an epidemiologist focused on exploring an integrative model of the psychological, behavioral, biological, and genetic aspects of mental health. The research plan addresses the intersection of two common and debilitating health conditions, Major Depression and Diabetes, that are leading sources of healthcare costs and public health burden in the US and globally. The public health significance of this research centers on understanding the etiologic relationships between mental and physical health in order to develop comprehensive programs to improve the health of persons with psychiatric disorders.

描述（由申请人提供）：流行病学和临床研究已经确定，重度抑郁症（MD）通常与晚年的医疗状况同时发生，包括代谢紊乱，如2型糖尿病（以下简称为“糖尿病”）。现在人们认识到，MD和糖尿病之间的相互关系可能是双向的。事实上，基于人群的队列研究中有一致的证据表明，MD与糖尿病和心血管疾病的风险和死亡率增加相关。然而，前瞻性研究无法明确区分MD是否是代谢紊乱的独特风险因素，或者这种现象是否是由于MD和糖尿病共有的共同因素，如遗传易感性，环境压力或全身生理失调。功能基因组学，特别是基因表达的评估，提供了一种新的手段，说明环境暴露如何与遗传易感性交叉影响生理。该职业发展奖（K 01）的广泛目标是调查共同发生的MD和糖尿病之间的病因关系，特别是遗传和环境风险源的结构和相对贡献。这项研究利用互补的方法来调查以下目标：首先，将使用潜在变量双胞胎模型来检查这种共病背后的广泛遗传和环境途径;其次，基因表达阵列将用于检查抑郁症状影响糖尿病风险的特定生物学途径。该研究计划的具体目标是：1）评估环境和遗传的贡献，以及它们之间的相互作用，成年后期MD和糖尿病之间的关系; 2）调查MD和糖尿病之间的行为途径，同时考虑共同的遗传责任; 3）检查抑郁症状和免疫相关基因表达之间的关系。候选人将接受负责任的研究，遗传流行病学和功能基因组学方面的培训。候选人建议在与精神病学，免疫学，功能基因组学，流行病学和生物统计学专家密切指导的培训期间实施该研究计划。拟议的培训计划将促进她过渡到独立的流行病学家，专注于探索心理，行为，生物和遗传方面的心理健康的综合模型。该研究计划解决了两种常见和令人衰弱的健康状况的交叉点，即严重抑郁症和糖尿病，这是美国和全球医疗保健成本和公共卫生负担的主要来源。这项研究的公共卫生意义在于了解精神和身体健康之间的病因关系，以便制定全面的计划来改善精神疾病患者的健康。