Oxidative insults, antioxidative responses and type 1 diabetes complications

氧化损伤、抗氧化反应和 1 型糖尿病并发症

• 批准号: 7736876
• 负责人: Tina Costacou
• 金额: $ 26.01万
• 依托单位: UNIVERSITY OF PITTSBURGH AT PITTSBURGH
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-09-01 至 2011-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7736876
• 关键词: Acute-Phase Proteins; Address; Age; Antioxidants; Area; Binding; Biological Markers; Blood Vessels; Cardiovascular system; Cells; Childhood; Clinical Trials; Complication; Complications of Diabetes Mellitus; Coronary Arteriosclerosis; Data; Development; Diabetes Mellitus; Diabetic Angiopathies; Diet; Distal; Documentation; Dose; Drug Formulations; Epidemiology; Etiology; Exhibits; Frequencies; Functional disorder; Gender; Genes; Genetic Polymorphism; Genetic Predisposition to Disease; Genotype; Glycosylated hemoglobin A; Goals; Gold; Hand; Haptoglobins; Heart Diseases; Hemoglobin; Human; Incidence; Individual; Inflammation; Injury; Insulin-Dependent Diabetes Mellitus; Intake; Intervention Trial; Isoprostanes; Kidney Diseases; Light; Lipid Peroxidation; Measurement; Measures; Methodology; Methods; Modification; Non-Insulin-Dependent Diabetes Mellitus; Oral Examination; Outcome; Oxidative Stress; Pancreas; Participant; Pathogenesis; Pathway interactions; Pattern; Persons; Plasma; Polyneuropathy; Population Characteristics; Populations at Risk; Prevention; Prospective Studies; Protein Binding; Public Health; Quality of life; Randomized Clinical Trials; Reactive Oxygen Species; Relative (related person); Reporting; Research; Research Design; Retinal Diseases; Risk; Risk Factors; Role; Sampling; Specificity; Supplementation; Testing; Time; Tissues; Tocopherols; Treatment Protocols; Vascular Diseases; Vitamin E; Vitamins; antioxidant therapy; base; calcium dependent sulfhydryl protease; cohort; cost; design; disorder risk; dosage; follow-up; improved; in vivo; inclusion criteria; oxidation; oxidative damage; prevent; protective effect; public health relevance; response; response to injury; success; urinary

DESCRIPTION (provided by applicant): The proposed study is based on an existing observational historical prospective study of childhood onset diabetes - the Pittsburgh Epidemiology of Diabetes Complications (EDC) Study. The focus is on oxidative stress and antioxidative defenses, the ultimate goal being to derive important background data which will be used to design an antioxidant trial in type 1 diabetes. The EDC is now in its 20th year of follow-up. Although a role for oxidative stress in diabetes complication incidence was proposed almost two decades ago, problems in the methods used to assess oxidative stress in vivo have prohibited definitive conclusions. Furthermore, despite the hypothesis that antioxidant vitamin supplementation could counteract oxidative stress, protecting against vascular disease, clinical trials results have generally not supported a protective effect of 1-tocopherol (the most active vitamin E form) supplementation on, especially, heart disease. Recent discoveries, however, may help shed light on the role of oxidative stress and antioxidant therapy in humans. On one hand, the ability to measure isoprostanes (IsoPs), currently considered the "gold standard" biomarker of oxidative stress, provides a better opportunity to understand this important pathway. Moreover, it has recently been proposed that antioxidant therapy may only be successful in those with specific Haptoglobin (Hp) genotypes. Hp, an acute phase protein, binds to free hemoglobin, inhibiting hemoglobin-induced oxidative tissue damage. As oxidative injury may contribute to the development of diabetes vascular complications, the Hp genotype could be a determinant of diabetic vascular disease risk. Our aim is to establish a profile of oxidative stress (urinary IsoPs) overtime among participants in the EDC study of type 1 diabetes. We further aim to assess whether the degree to which an individual is able to respond to oxidative stress (e.g. antioxidant intake/plasma levels and Hp genotype) modifies the risk associated with oxidative stress. Type 1 diabetes complications to be studied include proliferative retinopathy, confirmed distal symmetric polyneuropathy, overt nephropathy, and coronary artery disease. This proposal will entail: 1) the careful review of existing charts and more detailed documentation of antioxidant use, involving calling a number of participants for clarifications and details. Currently we have only documented use of vitamin supplements, lacking full information on dose and frequency of use; 2) the measurement of urinary IsoPs; and 3) the measurement of plasma 1-tocopherol from stored samples. Demonstrating that oxidative stress measures positively relate to the development of one or more of the proposed complications, and that plasma 1-tocopherol levels inversely relate to complications and/or modify the oxidative stress component would greatly strengthen the argument for a trial. Furthermore, examination of the oral dose/plasma level association for vitamin E intake/1-tocopherol levels will yield some data as to the appropriate dosage. Finally, the effects of Hp genotype on all of these outcomes will greatly influence the likely inclusion criteria for an intervention trial. PUBLIC HEALTH RELEVANCE: The significance of this proposal lies in the ability to provide, in a large type 1 diabetes cohort, evidence for: i) the role of oxidative stress in the pathogenesis of vascular disease, ii) the potential utility of antioxidant supplementation in decreasing levels of oxidative stress, and iii) the potential role of genetic susceptibility in both assessing disease risk and in identifying at risk populations with the potential to benefit from antioxidant treatment. Thus, this project may provide information for a relatively inexpensive regimen for the prevention of vascular complications among susceptible individuals with diabetes, improving their quality of life and reducing cost associated with the presence of complications.

描述（由申请方提供）：拟定研究基于现有的儿童期发病糖尿病观察性历史前瞻性研究-匹兹堡糖尿病并发症流行病学（EDC）研究。重点是氧化应激和抗氧化防御，最终目标是获得重要的背景数据，这些数据将用于设计1型糖尿病的抗氧化试验。EDC现在已经进入了第20个随访年。虽然氧化应激在糖尿病并发症发病率中的作用是在近二十年前提出的，但用于评估体内氧化应激的方法中存在的问题阻碍了明确的结论。此外，尽管假设抗氧化维生素补充剂可以抵消氧化应激，防止血管疾病，但临床试验结果通常不支持1-生育酚（最活跃的维生素E形式）补充剂对心脏病的保护作用。然而，最近的发现可能有助于阐明氧化应激和抗氧化治疗在人类中的作用。一方面，测量目前被认为是氧化应激的“金标准”生物标志物的异前列烷（IsoPs）的能力为理解这一重要途径提供了更好的机会。此外，最近有人提出，抗氧化治疗可能只在那些特定的结合珠蛋白（Hp）基因型的成功。幽门螺杆菌是一种急性时相蛋白，与游离血红蛋白结合，抑制血红蛋白诱导的组织氧化损伤。由于氧化损伤可能导致糖尿病血管并发症的发生，Hp基因型可能是糖尿病血管疾病风险的决定因素。我们的目的是在EDC研究的1型糖尿病参与者中建立一个氧化应激（尿IsoPs）随时间变化的概况。我们进一步旨在评估个体对氧化应激的反应程度（例如抗氧化剂摄入量/血浆水平和Hp基因型）是否会改变与氧化应激相关的风险。待研究的1型糖尿病并发症包括增殖性视网膜病变、确诊的远端对称性多发性神经病、显性肾病和冠状动脉疾病。这一提议将需要：1）仔细审查现有图表和更详细的抗氧化剂使用文件，包括致电一些参与者进行澄清和详细说明。目前，我们仅记录了维生素补充剂的使用，缺乏关于剂量和使用频率的完整信息; 2）尿IsoP的测量;和3）来自储存样品的血浆1-生育酚的测量。证明氧化应激措施与一种或多种拟定并发症的发生呈正相关，血浆1-生育酚水平与并发症呈负相关和/或改变氧化应激组分将大大加强试验的论据。此外，检查维生素E摄入量/1-生育酚水平的口服剂量/血浆水平相关性将产生一些关于适当剂量的数据。最后，Hp基因型对所有这些结果的影响将极大地影响干预试验的可能入选标准。公共卫生关系：该建议的重要性在于能够在大型1型糖尿病队列中提供以下证据：i）氧化应激在血管疾病发病机制中的作用，ii）补充抗氧化剂在降低氧化应激水平中的潜在效用，以及iii）遗传易感性在评估疾病风险和识别有可能受益于以下疾病的风险人群中的潜在作用：抗氧化处理因此，该项目可以提供一个相对便宜的方案，用于预防糖尿病易感人群的血管并发症，提高他们的生活质量，降低与并发症相关的费用。