Randomized trial of vitamin D and omega-3 fatty acids for diabetic kidney disease

维生素 D 和 omega-3 脂肪酸治疗糖尿病肾病的随机试验

• 批准号: 8330295
• 负责人: Ian H de Boer
• 金额: $ 34.14万
• 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: 2010-09-01 至 2015-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8330295
• 关键词: 25-hydroxyvitamin D; Accounting; Acids; Affect; Age; Albumins; Albuminuria; Amplifiers; Ancillary Study; Animals; Benefits and Risks; Blood Vessels; Blood specimen; C-reactive protein; Cardiovascular Diseases; Cardiovascular system; Cessation of life; Cholecalciferol; Clinical; Clinical Trials; Complications of Diabetes Mellitus; Controlled Clinical Trials; Creatinine; Data; Development; Diabetes Mellitus; Diabetic Nephropathy; Diabetic Retinopathy; Docosahexaenoic Acids; Eicosapentaenoic Acid; Elderly; End stage renal failure; Enrollment; Evaluation; Event; Experimental Animal Model; Funding; Glomerular Filtration Rate; Glycosylated hemoglobin A; Goals; Health; Human; Impairment; Inflammation; Intervention; Intervention Studies; Kidney; Kidney Diseases; Laboratories; Mails; Malignant Neoplasms; Marines; Measurement; Meta-Analysis; Morbidity - disease rate; Omega-3 Fatty Acids; Outcome; Oxidative Stress; Parents; Participant; Persons; Placebo Control; Placebos; Plasma; Population; Prevalence; Primary Prevention; Public Health; Randomized; Randomized Clinical Trials; Recruitment Activity; Renin-Angiotensin-Aldosterone System; Research; Research Design; Research Infrastructure; Risk Factors; Running; Sample Size; Schedule; Serum; Severities; Testing; Time; Translating; United States; United States National Institutes of Health; Urine; Vitamin D; Woman; adjudicate; aging population; base; cardiovascular disorder risk; cardiovascular risk factor; clinically relevant; cohort; cost; design; diabetic; disorder prevention; double-blind placebo controlled trial; effective intervention; follow-up; glomerulosclerosis; glycemic control; high risk; improved; inhibitor/antagonist; meetings; men; mortality; novel; post gamma-globulins; premature; prevent; public health relevance; randomized placebo controlled trial; randomized trial; research study

DESCRIPTION (provided by applicant): We propose a randomized, placebo-controlled clinical trial of vitamin D3 (cholecalciferol) and omega-3 fatty acids (eicosapentaenoic acid plus docosahexaenoic acid) to prevent the development and progression of diabetic kidney disease (DKD). Persons with diabetes are at high risk of developing kidney disease, and DKD is both the leading cause of end stage renal disease in the developed world and a potent amplifier of cardiovascular disease risk. Vitamin D and omega-3 fatty acids are promising interventions for DKD prevention and treatment, based on results of animal-experimental models and early human studies. Because these interventions are relatively safe, inexpensive, and widely available, they may offer opportunity to substantially reduce the burden of DKD in large populations. We aim to test whether vitamin D3 and/or omega-3 fatty acids prevent progression of albuminuria and loss of glomerular filtration rate, two complementary manifestations of DKD, over 4 years of treatment. To effectively and efficiently test study hypotheses, we propose an ancillary study to the Vitamin D and Omega-3 Trial (VITAL), an NIH-funded randomized clinical trial. In VITAL, 20,000 participants (men ages e 60 years, women ages e 65 years) will be randomly assigned in a 2x2 factorial design to vitamin D3 (cholecalciferol) 1600 IU daily versus placebo, and to eicosapentaenoic acid 500 mg plus docosahexaenoic acid 500 mg daily versus placebo, and followed for a mean of 5 years to assess effects on cardiovascular disease and cancer events. Leveraging the established infrastructure of VITAL, we propose to identify and recruit a sub-cohort of 1,500 VITAL participants with diabetes at baseline and to ascertain effects of study interventions on albuminuria and glomerular filtration rate in this group. Following the simple and cost-efficient design of the parent VITAL trial, biospecimens will be collected locally and delivered to the VITAL central laboratory by mail. First morning voids will be collected at baseline and year 4 for measurement of urine albumin-creatinine ratio. Blood samples will be collected simultaneously for measurement of glomerular filtration rate (using serum creatinine and cystatin C), 25- hydroxyvitamin D, eicosapentaenoic acid plus docosahexaenoic acid, C-reactive protein, and hemoglobin A1c. The proposed studies are designed to determine whether vitamin D3 and/or omega-3 fatty acids have causal and clinically relevant effects on the development and progression of DKD. PUBLIC HEALTH RELEVANCE: Diabetic kidney disease (DKD) is a cause of substantial morbidity and mortality. Despite widespread use of intensive glycemic control and renin-angiotensin-aldosterone system inhibitors, renal and cardiovascular consequences of DKD remain common. This study will evaluate whether vitamin D3 and/or omega-3 fatty acids are safe and effective interventions to reduce the burden of DKD among the large and growing diabetic population.

描述（由申请人提供）：我们建议进行一项随机、安慰剂对照的临床试验，使用维生素D3（胆钙化醇）和omega-3脂肪酸（二十碳五烯酸加二十二碳六烯酸）来预防糖尿病肾病（DKD）的发生和进展。糖尿病患者患肾脏疾病的风险很高，DKD既是发达国家终末期肾脏疾病的主要原因，也是心血管疾病风险的有力放大器。根据动物实验模型和早期人体研究的结果，维生素D和omega-3脂肪酸是预防和治疗DKD的有希望的干预措施。由于这些干预措施相对安全、价格低廉且可广泛获得，它们可能为大量人群大幅减轻DKD负担提供机会。我们的目标是测试维生素D3和/或omega-3脂肪酸是否能在4年的治疗中预防蛋白尿的进展和肾小球滤过率的丧失，这是DKD的两个互补表现。为了有效和高效地检验研究假设，我们提出了维生素D和Omega-3试验（VITAL）的辅助研究，这是一项美国国立卫生研究院资助的随机临床试验。在VITAL试验中，20,000名参与者（男性60岁，女性65岁）将被随机分配到每天1600 IU的维生素D3（胆钙化醇）组，与安慰剂组相比，每天500 mg的二十碳五烯酸加500 mg的二十二碳六烯酸组，与安慰剂组相比，平均随访5年，以评估对心血管疾病和癌症事件的影响。利用VITAL已建立的基础设施，我们建议确定并招募一个由1500名基线时患有糖尿病的VITAL参与者组成的亚队列，并确定研究干预对该组蛋白尿和肾小球滤过率的影响。根据母体VITAL试验的简单和经济高效的设计，生物标本将在当地收集，并通过邮寄方式送到VITAL中心实验室。第一次早晨排尿将在基线和第4年收集，用于测量尿白蛋白-肌酐比率。同时采集血样，测定肾小球滤过率（使用血清肌酐和胱抑素C）、25-羟基维生素D、二十碳五烯酸加二十二碳六烯酸、C反应蛋白和血红蛋白A1c。拟议的研究旨在确定维生素D3和/或omega-3脂肪酸是否对DKD的发生和进展有因果关系和临床相关的影响。