Insulin Resistance in Chronic Kidney Disease

慢性肾脏病的胰岛素抵抗

• 批准号: 8634621
• 负责人: Ian H de Boer
• 金额: $ 14.67万
• 依托单位: UNIVERSITY OF WASHINGTON
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-08-15 至 2015-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8634621
• 关键词: Address; Affect; American; Applications Grants; Beta Cell; Biology; Biometry; Body Composition; Calcitriol; Cardiovascular Diseases; Cardiovascular system; Catabolism; Cause of Death; Cell physiology; Cessation of life; Chronic Kidney Failure; Clinical Research; Clinical Trials; Epidemiologic Studies; Equation; Euglycemic Clamping; Event; Fasting; Financial compensation; Foundations; Functional disorder; Funding; Future; General Population; Glomerular Filtration Rate; Glucose; Glucose Clamp; Glucose Intolerance; Goals; Gold; Health; High Prevalence; Individual; Inflammation; Institutes; Insulin; Insulin Resistance; Kidney; Kidney Failure; Measurement; Measures; Metabolic; Metabolic acidosis; Metabolism; Methodology; Methods; Morbidity - disease rate; OGTT; Outcome; Oxidative Stress; Pathway interactions; Patients; Persons; Physiological; Physiology; Population; Population Study; Public Health; Reactive Oxygen Species; Research Institute; Resistance; Resources; Risk Factors; Risk Reduction; Severities; Skeletal Muscle; Staging; Structure of beta Cell of islet; Testing; Therapeutic Intervention; Time; Toxin; United States; Universities; Washington; Work; arterial stiffness; base; cardiovascular disorder prevention; cardiovascular disorder risk; cardiovascular risk factor; design; fasting glucose; glucose tolerance; high risk; improved; innovation; insulin sensitivity; intravenous glucose tolerance test; mortality; multidisciplinary; novel; nutrition; receptor; response; sound; statistics; therapeutic target; translational health science

Chronic kidney disease (CKD) affects up to 26 million Americans, or 13% of the United States population. Moderate-severe CKD (stage 3-4, defined by glomerular filtration rate 15-59 mL/min/1.73m2) has a particularly large public health impact because it is most prevalent and because it potently amplifies risk of cardiovascular disease. Specifically, individuals with moderate-severe CKD have important "non-traditional" risk factors for cardiovascular disease which are not adequately addressed by risk reduction strategies developed for the general population. Insulin resistance is one "non-traditional" mechanism through which CKD may cause cardiovascular disease. In CKD, post-receptor resistance to insulin action in skeletal muscle is commonly acquired due to unique metabolic abnormalities, including impaired renal calcitriol synthesis, metabolic acidosis, and accumulation of uremic toxins. In turn, insulin resistance may promote cardiovascular disease by impairing endothelial function, increasing reactive oxygen species, and exacerbating systemic inflammation. The metabolic abnormalities unique to CKD fundamentally alter the pathophysiology and ascertainment of insulin resistance and offer novel potential targets for therapeutic intervention. The overall goal of this grant application is to comprehensively characterize insulin resistance in moderate- severe CKD. First, we propose to define the severity of insulin resistance, the compensatory response of the pancreatic beta cell, and net effects on glucose tolerance, which are currently poorly understood, using gold standard methods (hyperinsulinemic euglycemic clamp, intravenous glucose tolerance test, oral glucose tolerance test). Second, we propose to develop and validate formulae estimating insulin resistance for use in future epidemiologic studies and clinical trials. Third, we propose to test associations of insulin resistance with endothelial function, oxidative stress, and inflammation. To accomplish these goals, we have assembled a multidisciplinary team with expertise in the biology of CKD, metabolism, quantitative assessment of insulin sensitivity and beta-cell function, nutrition, and biostatistics. As part of this innovative collaborative approach, this study will take advantage of existing resources at the University of Washington and the Kidney Research Institute in Seattle. These include the Institute for Translational Health Sciences Clinical Research Center, Nutrition and Body Composition Core, and Center for Biomedical Statistics.

慢性肾脏疾病（CKD）影响着多达2600万美国人，占美国人口的13%。中重度CKD（3-4期，定义为肾小球滤过率15-59 mL/min/1.73m2）具有特别大的公共卫生影响，因为它是最普遍的，因为它可能会增加心血管疾病的风险。具体来说，患有中重度CKD的个体具有重要的心血管疾病“非传统”风险因素，而这些因素在为普通人群制定的风险降低策略中没有得到充分解决。胰岛素抵抗是CKD可能导致心血管疾病的一种“非传统”机制。在CKD中，骨骼肌对胰岛素作用的受体后抵抗通常是由于独特的代谢异常而获得的，包括肾骨化三醇合成受损、代谢性酸中毒和尿毒症毒素积累。反过来，胰岛素抵抗可能通过损害内皮功能、增加活性氧和加重全身炎症来促进心血管疾病。CKD特有的代谢异常从根本上改变了胰岛素抵抗的病理生理和确定，并为治疗干预提供了新的潜在靶点。这项拨款申请的总体目标是全面表征中重度CKD患者的胰岛素抵抗。首先，我们建议使用金标准方法（高胰岛素正糖钳、静脉葡萄糖耐量试验、口服葡萄糖耐量试验）确定胰岛素抵抗的严重程度、胰腺β细胞的代偿反应以及对葡萄糖耐量的净影响，这些目前尚不清楚。其次，我们建议开发和验证估算胰岛素抵抗的公式，用于未来的流行病学研究和临床试验。第三，我们建议测试胰岛素抵抗与内皮功能、氧化应激和炎症的关系。为了实现这些目标，我们组建了一个多学科的团队，他们在CKD生物学、代谢、胰岛素敏感性和β细胞功能的定量评估、营养和生物统计学方面具有专业知识。作为这种创新合作方法的一部分，这项研究将利用华盛顿大学和西雅图肾脏研究所的现有资源。这些机构包括转化健康科学研究所临床研究中心、营养和身体成分核心以及生物医学统计中心。