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Rationale and design of a clinical trial to evaluate metformin and colesevelam HCl as first-line therapy in type 2 diabetes and colesevelam HCl in prediabetes.

机译:临床试验的理由和设计,以评估二甲双胍和薏仁舒姆HCL作为2型糖尿病患者的一线治疗。

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OBJECTIVE: The complications of type 2 diabetes mellitus (DM) can begin early in the progression from impaired glucose tolerance to type 2 DM. Metformin is recommended as initial drug therapy for managing hyperglycemia in type 2 DM. The bile acid sequestrant colesevelam hydrochloride (HCl) is approved in the United States for glycemic control in adults with type 2 DM. Colesevelam HCl improves glycemic control and reduces low-density lipoprotein-cholesterol in patients inadequately controlled on metformin-, sulfonylurea-, or insulin-based therapy. This trial is designed to evaluate whether initial therapy with metformin + colesevelam HCl provides greater glucose control and additional lipid and lipoprotein benefits, as compared to metformin alone in drug-naive patients with type 2 DM, and whether treatment with colesevelam HCl has a beneficial effect on lipid and glucose levels in drug-naive patients with impaired glucose tolerance and/or impaired fasting glucose (prediabetes). RESEARCH DESIGN AND METHODS: In this multicenter, randomized, double-blind, placebo-controlled, parallel-group trial, drug-naive patients with type 2 DM will be randomized 1 : 1 to metformin + colesevelam HCl or metformin + matching placebo, while those with prediabetes will be randomized 1 : 1 to colesevelam HCl or placebo, for 16 weeks of treatment. The primary efficacy endpoint will be change in glycosylated hemoglobin (HbA(1c)) in patients with type 2 DM and change in low-density lipoprotein-cholesterol levels in patients with prediabetes. CONCLUSION: A potential limitation is that there is no direct comparator for the dual glucose- and lipid-lowering effect of colesevelam HCl in the prediabetes cohort. However, results of this trial will help to define the extent to which colesevelam HCl can help improve cardiometabolic risk factors for complications of type 2 DM in the first-line environment, and will also indicate the extent to which early intervention with colesevelam HCl can help to correct metabolic abnormalities associated with prediabetes.
机译:目的:2型糖尿病(DM)的并发症可以从葡萄糖耐量损伤到2 dm的血糖耐受性早期开始。二甲双胍被推荐为初始药物治疗,用于管理2 DM中的高血糖症。胆汁酸螯合体Colesevelam盐酸盐(HCl)在美国批准在2 dm的成人中进行血糖控制。 Colesevelam HCl改善血糖控制,并减少患者在二甲双胍,磺酰脲类或基于胰岛素的疗法上不充分控制的患者中的低密度脂蛋白 - 胆固醇。该试验旨在评估与二甲双胍+ Colesevelam HCl的初始治疗是否提供了更大的葡萄糖对照和额外的脂质和脂蛋白益处,而单独的二甲双胍含有2DM的患者,以及与Colesevelam HCL治疗是否具有有益效果在葡萄糖耐量受损和/或空腹血糖受损(PrediaBetes)的脂质和葡萄糖水平上的脂质和血糖水平。研究设计和方法:在该多中心,随机,双盲,安慰剂控制,并联群试验中,2 DM型毒药 - 天真患者将随机化1:1至二甲双胍+ Colesevelam HCl或二甲双胍+匹配安慰剂,同时含有预先奶油的人将是1:1至Colesevelam HCl或安慰剂,治疗16周。初级疗效终点将在患有2 dm型患者的糖基化血红蛋白(HBA(1C))中的变化,并在患有前奶酪患者的低密度脂蛋白 - 胆固醇水平的变化。结论:潜在的限制是,在Prediabetes队列中,Colesevelam HCL的双葡萄糖和脂质降低效果没有直接比较。然而,该试验的结果将有助于确定Colesevelam HCL在一线环境中为2 dm的并发症提高心脏异构危险因素的程度,并且还将表明与Colesevelam HCL早期干预的程度可以帮助纠正与前驱奶油相关的代谢异常。

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