Acarbose compared with metformin as initial therapy in patients with newly diagnosed type 2 diabetes: an open-label, non-inferiority randomised trial

阿卡波糖 医学 二甲双胍 2型糖尿病 打开标签 内科学 糖尿病 随机对照试验 梅德林 内分泌学 政治学 法学
作者
Wenying Yang,Jie Liu,Zhongyan Shan,Haoming Tian,Zhiguang Zhou,Qiuhe Ji,Jianping Weng,Weiping Jia,Juming Lu,Jing Liu,Yuan Xu,Zhaojun Yang,Wei Chen
出处
期刊:The Lancet Diabetes & Endocrinology [Elsevier BV]
卷期号:2 (1): 46-55 被引量:155
标识
DOI:10.1016/s2213-8587(13)70021-4
摘要

Background Metformin is the only first-line oral hypoglycaemic drug for type 2 diabetes recommended by international guidelines with proven efficacy, safety, and cost-effectiveness. However, little information exists about its use in Asian populations. We aimed to ascertain the effectiveness of the α-glucosidase inhibitor acarbose, extensively adopted in China, compared with metformin as the alternative initial therapy for newly diagnosed type 2 diabetes. Methods In this 48-week, randomised, open-label, non-inferiority trial, patients who were newly diagnosed with type 2 diabetes, with a mean HbA1c of 7·5%, were enrolled from 11 sites in China. After a 4-week lifestyle modification run-in, patients were assigned to 24 weeks of monotherapy with metformin or acarbose as the initial treatment, followed by a 24-week therapy phase during which add-on therapy was used if prespecified glucose targets were not achieved. Primary endpoints were to establish whether acarbose was non-inferior to metformin in HbA1c reduction at week 24 and week 48 timepoints. The non-inferiority margin was 0·3%, with an expected null difference in the change from baseline to week 48 in HbA1c. Analysis was done on a modified intention-to-treat population. This study was registered with Chinese Clinical Trial Registry, number ChiCTR-TRC-08000231. Findings Of the 788 patients randomly assigned to treatment groups, 784 patients started the intended study drug. HbA1c reduction at week 24 was −1·17% in the acarbose group and −1·19% in the metformin group. At week 48, the HbA1c reduction was −1·11% (acarbose) and −1·12% (metformin) with difference 0·01% (95% CI −0·12 to 0·14, p=0·8999). Six (2%) patients in the acarbose group and seven (2%) patients in the metformin group had serious adverse events, and two (1%) and four (1%) had hypoglycaemic episodes. Interpretation This study provides evidence that acarbose is similar to metformin in efficacy, and is therefore a viable choice for initial therapy in Chinese patients newly diagnosed with type 2 diabetes. Funding Bayer Healthcare (China) and Double Crane Phama.
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