Assessment of the Production of Uremic Toxins by the Gut Microbiota of Patients With Chronic Kidney Disease: in Vitro Test
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 20
- 试验地点
- 2
- 主要终点
- Production of precursor of one of major uremic toxins: indole
研究概览
简要总结
Chronic renal failure (CKD) affects 3 million people in France and is characterized by the accumulation of uremic toxins (UTs) such as p-cresyl sulfate (PCS) and indoxyl sulfate (IS) which participate in cardiovascular complications and disturbance of the carbohydrate metabolism associated with CKD. These UTs are not eliminated by dialysis due to their high affinity for albumin and alternative strategies to dialysis must be developed to decrease the production of TUs in patients not yet in dialysis. The dysregulation of the intestinal microbiota observed during CKD increases the generation of UTs in the intestine, by the transformation of amino acids derived from proteins (such as tyrosine and tryptophan transformed respectively into PCS and, IS). Thus, modulation of the intestinal microbiota seems to be an attractive target for reducing the production of UTs and the comorbidities associated with CKD. Some studies have demonstrated the potential interest of probiotics in lowering the plasma concentration of UTs, but the effects remain unclear. In order to test the interest of probiotics during CKD, the investigators have, in collaboration with the Nestlé laboratory and the ProDigest platform, the possibility of testing probiotics using a human intestine simulator before the investigation of experimental and human models. For this the investigators would need a collection of fresh stools. The fresh stools will be instilled in artificial intestine to test the efficacy of selected probiotics on UTs production.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Age between 18 and 80 years old
- •Non diabetic (fasting blood glucose <1.26 g / L, or lack of insulin or oral antidiabetic treatment)
- •BMI between 18 and 30 kg / m²
- •Patient with CKD stage 4-5 ( eDFG < 30 ml/min/1.73m2 CKD-EPI)
- •Not dialyzed
- •No history of kidney transplant
- •Patient followed in the nephrology department of Pr FOUQUE at the Lyon Sud hospital center
排除标准
- •Active inflammatory, infectious, cardiovascular or neoplastic disease
- •Colectomy, resection of the small intestine or cholecystectomy
- •Patient having received antibiotics, prebiotics, probiotics in the last 3 months.
- •Patient using laxatives (more than 2 doses per day for the last 3 months)
- •Known renal pathology or known urologic malformation (healthy volunteer only)
结局指标
主要结局
Production of precursor of one of major uremic toxins: indole
时间窗: Indoles production will be measured 48 hours after instillation of fresh feces in the artificial intestine
The main endpoint is the concentration of the precursor of indoxyl sulfate (indole) in the lumen of the artificial intestine with a microbiota of a patient with CKD compared to the concentration of indol in the lumen of artificial intestine with a microbiota from a patient with CKD and supplemented with a probiotic (supplied by Nestlé)
次要结局
- Intestinal microbiota composition(48 hours after instillation of fresh feces in the human intestine simulator)
- Uremic toxins production(48 hours after instillation of fresh feces in the human intestine simulator)
- Intestinal permeability in a human intestine simulator(48 hours after instillation of fresh feces in the human intestine simulator)
- Production of short-chain fatty acids (SCFA)(48 hours after instillation of fresh feces in the human intestine simulator)
- Biochemical parameters(48 hours after instillation of fresh feces in the human intestine simulator)