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Effect of prebiotic intake on gut microbiota, intestinal permeability and glycemic control in children with type 1 diabetes: study protocol for a randomized controlled trial

机译:益生元摄入对1型糖尿病儿童肠道菌群,肠道通透性和血糖控制的影响:一项随机对照试验的研究方案

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Background The gut microbiome is increasingly recognized as a contributor to disease states. Patients with type 1 diabetes (DM1) have distinct gut microbiota in comparison to non-diabetic individuals, and it has been linked to changes in intestinal permeability, inflammation and insulin resistance. Prebiotics are non-digestible carbohydrates that alter gut microbiota and could potentially improve glycemic control in children with DM1. This pilot study aims to determine the feasibility of a 12-week dietary intervention with prebiotics in children with DM1. Methods/design This pilot study is a single-centre, randomized, double-blind, placebo-controlled trial in children aged 8 to 17?years with DM1 for at least one year. Participants will be randomized to receive either placebo (maltodextrin 3.3?g orally/day) or prebiotics (oligofructose-enriched inulin 8?g orally/day; Synergy1, Beneo, Mannheim, Germany). Measures to be assessed at baseline, 3?months and 6?months include: anthropometric measures, insulin doses/regimens, frequency of diabetic ketoacidosis, frequency of severe hypoglycemia, average number of episodes of hypoglycemia per week, serum C-peptide, HbA1c, serum inflammatory markers (IL-6, IFN-gamma, TNF-alpha, and IL-10), GLP-1 and GLP-2, intestinal permeability using urine assessment after ingestion of lactulose, mannitol and 3-O-methylglucose, and stool sample collection for gut microbiota profiling. Discussion This is a novel pilot study designed to test feasibility for a fully powered study. We hypothesize that consumption of prebiotics will alter gut microbiota and intestinal permeability, leading to improved glycemic control. Prebiotics are a potentially novel, inexpensive, low-risk treatment addition for DM1 that may improve glycemic control by changes in gut microbiota, gut permeability and inflammation. Trial registration ClinicalTrials.gov: NCT02442544 . Registered on 10 March 2015.
机译:背景技术肠道微生物组已被越来越多地认为是导致疾病的原因。与非糖尿病患者相比,患有1型糖尿病(DM1)的患者具有独特的肠道菌群,并且与肠道通透性,炎症和胰岛素抵抗的变化有关。益生元是不可消化的碳水化合物,可改变肠道菌群,并可能改善DM1儿童的血糖控制。这项初步研究旨在确定在DM1患儿中使用益生元进行12周饮食干预的可行性。方法/设计这项初步研究是一项单中心,随机,双盲,安慰剂对照试验,针对年龄在8至17岁的DM1患儿至少一年。参与者将被随机分配接受安慰剂(麦芽糊精3.3克/天口服)或益生元(富含低聚果糖的菊粉8克/天口服; Synergy1,Beneo,曼海姆,德国)。在基线,3个月和6个月时要评估的措施包括:人体测量,胰岛素剂量/方案,糖尿病酮症酸中毒的频率,严重低血糖的频率,每周平均低血糖发作的次数,血清C肽,HbA1c,血清炎性标志物(IL-6,IFN-γ,TNF-α和IL-10),GLP-1和GLP-2,摄入乳果糖,甘露醇和3-O-甲基葡萄糖后尿液评估得出的肠通透性和粪便肠道菌群分析的样品收集。讨论这是一项新颖的试点研究,旨在测试功能全面的研究的可行性。我们假设食用益生元会改变肠道菌群和肠道通透性,从而改善血糖控制。益生元是DM1的一种潜在的新颖,廉价,低风险的治疗药物,可通过改变肠道菌群,肠道通透性和炎症来改善血糖控制。试用注册ClinicalTrials.gov:NCT02442544。 2015年3月10日注册。

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