PoGlyDRI - Impact of Dietary Polyphenols on Protein Glycation in Type 2 Diabetes Mellitus Subjects With Chronic Renal Insufficiency
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 9
- 试验地点
- 2
- 主要终点
- Change in estimated glomerular filtration rate (eGFR)
研究概览
简要总结
Type 2 diabetes mellitus (T2DM) is associated with an increased risk of kidney failure, with high levels of glycohaemoglobin (HbA1c) presenting a sharper decline in renal function and an increase in the risk of mortality and end-stage renal disease (ESRD). Polyphenols may improve renal insufficiency in patients with diabetes with chlorogenic acids (CGA) one of the principle polyphenol groups in the diet - coffee/tea, stone fruits (especially plums/prunes) and some vegetables (artichoke, chicory). CGA (3-4 cups of coffee) has been associated with 25% lower risk of T2DM and a favourable reduction of HbA1c, blood pressure, and oxidative stress levels. This randomised controlled trial, therefore, aims to evaluate the effect of high CGA food on glycation and oxidative stress in T2DM subjects with early renal insufficiency (glomerular filtration rate of 35-60 mL/min) as well as progression of renal insufficiency and the risk of cardiovascular diseases.
The study will have two phases - phase I, an interventional study of 3 months followed by phase II, an observational study of 21 months.
In phase I, subjects will be randomized into 2 groups: CGA-enriched diet group, or control (habitual) diet group. The treatment group will be provided with a chlorogenic acid-rich food (coffee) with instructions to achieve an intake of 400 mg per day (equivalent to 3-4 coffee cups per day) for 12 weeks. The control group will receive a conventional coffee low in chlorogenic acid.
Participants will attend three sessions during phase I; baseline, 6 weeks, and 12 weeks. At baseline, general information, medical history, dietary habits and medication use will be recorded and a Food Frequency Questionnaire completed. Urine and blood samples will be collected and blood pressure, waist circumference, height and weight recorded. Participants' diet over the previous 3 days will be assessed by estimated food diary analysis.
In phase II, written dietary recommendations will be provided at three time points (months 6, 12 and 24) - treatment group to achieve a CGA-rich diet (total polyphenol intake of at least 1g per day, and at least 400mg per day of CGA) and standard dietary advice for the control group. Anthropometric/dietary data will be collected as well as blood and urine samples to assess markers of renal function, glycation and oxidative stress, and proteomic markers of cardiovascular disease, coronary artery disease and diabetes.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 40 Years 至 80 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •type 2 Diabetes Mellitus
- •chronic renal insufficiency with persistent eGFR of 35-60mL/min for at least three months
- •fluent in English
排除标准
- •dialysis therapy (current or previous)
- •malignancy
- •transplant recipient
- •hyperthyroidism
- •hypothyroidism
- •high dose glucocorticoids (≥250 mg)
- •body mass index (BMI) ≥ 45 kg/m2
- •special dietary requirements
- •take creatine, antioxidants or vitamin supplements
- •consume >4 cups of tea/coffee per day
- •consume >5 portion of fruits and vegetables per day
结局指标
主要结局
Change in estimated glomerular filtration rate (eGFR)
时间窗: 21 months
Change in glycohaemoglobin (HbA1c)
时间窗: 3 months
次要结局
- Change in Urinary Albumin Excretion(21 months)
- Change in blood pressure(21 months)
- Change in crystatin C(21 months)
- Change in fasting glucose(3 months)
- Change in creatinine(21 months)
- Change in soluble receptor for AGE (sRAGE)(3 months)
- Change in F2-isoprostane(3 months)
- Change in cholesterol(21 months)
- Change in 8hydroxy 2'deoxyguanoside (8OhdG)(21 months)
- Change in advanced glycation end product (AGE)(3 months)
- Change in thiobarbituric acid reactive substances (TBARS)(21 months)
- Change in malondialdehyde (MDA)(3 months)
- Change in Interleukin-6(21 months)
- Change in fructosamine(3 months)
- Change in fibrinogen(21 months)
- Change in C-reactive protein(21 months)
- Change in advanced oxidation protein products (AOPP)(21 months)
