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一项评估二甲双胍和盐酸考来维仑作为2型糖尿病一线治疗药物以及盐酸考来维仑作为糖尿病前期治疗药物的临床试验的原理与设计。

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.

作者信息

Jones Michael R, Mudaliar Sunder, Hernandez-Triana Eric, Unnikrishnan Ambika G, Lai Yu-Ling, Abby Stacey L, Misir Soamnauth, Jin Xiaoping, Nagendran Sukumar

机构信息

Daiichi Sankyo Inc, Parsippany, NJ 07054, USA.

出版信息

Curr Med Res Opin. 2009 Sep;25(9):2239-49. doi: 10.1185/03007990903126791.

Abstract

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-naïve patients with type 2 DM, and whether treatment with colesevelam HCl has a beneficial effect on lipid and glucose levels in drug-naïve 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-naïve 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.

摘要

目的

2型糖尿病(DM)的并发症在从糖耐量受损进展至2型DM的早期即可出现。二甲双胍被推荐作为2型DM患者管理高血糖的初始药物治疗。胆汁酸螯合剂盐酸考来维仑在美国被批准用于2型DM成人患者的血糖控制。盐酸考来维仑可改善血糖控制,并降低接受二甲双胍、磺脲类或胰岛素治疗但控制不佳患者的低密度脂蛋白胆固醇水平。本试验旨在评估,与单纯使用二甲双胍相比,二甲双胍+盐酸考来维仑初始治疗对初治的2型DM患者是否能提供更好的血糖控制以及额外的血脂和脂蛋白益处,以及盐酸考来维仑治疗对糖耐量受损和/或空腹血糖受损(糖尿病前期)的初治患者的血脂和血糖水平是否有有益影响。

研究设计与方法

在这项多中心、随机、双盲、安慰剂对照、平行组试验中,初治的2型DM患者将按1:1随机分为二甲双胍+盐酸考来维仑组或二甲双胍+匹配安慰剂组,而糖尿病前期患者将按1:1随机分为盐酸考来维仑组或安慰剂组,进行为期16周的治疗。主要疗效终点为2型DM患者糖化血红蛋白(HbA1c)的变化以及糖尿病前期患者低密度脂蛋白胆固醇水平的变化。

结论

一个潜在的局限性是,在糖尿病前期队列中,没有针对盐酸考来维仑双重降糖和降脂作用的直接对照。然而,本试验的结果将有助于确定盐酸考来维仑在一线治疗环境中可在多大程度上帮助改善2型DM并发症的心血管代谢危险因素,也将表明早期使用盐酸考来维仑干预可在多大程度上帮助纠正与糖尿病前期相关的代谢异常。

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