Division of Endocrinology, Diabetes and Metabolism, Baylor College of Medicine, Houston, TX 77030, USA.
Diabetes Obes Metab. 2012 Apr;14 Suppl 2:13-9. doi: 10.1111/j.1463-1326.2012.01574.x.
The glucagon-like peptide-1 (GLP-1) receptor agonist liraglutide is indicated as an add-on to oral antidiabetic drug regimens in subjects with type 2 diabetes. Herein, the results of clinical trials assessing the efficacy, safety and tolerability of liraglutide when used in combination with either one or two oral antidiabetic therapies are summarised, then contrasted with the effects of exenatide and dipeptidyl peptidase (DPP-4) inhibitors. GLP-1 receptor agonists lead to effective glycaemic control when used as combination therapy with either one or two oral antidiabetic agents, and may confer overall benefits in weight loss and blood pressure in some subjects. These agents are well tolerated; the most commonly reported adverse effect is mild-to-moderate gastrointestinal symptoms, which are usually transient. Rates of hypoglycaemia in these trials were low, although higher rates were noted when combined with a sulphonylurea. While further study will be required, GLP-1 receptor agonists may offer important advantages over other diabetic therapies, including DPP-4 inhibitors.
胰高血糖素样肽-1(GLP-1)受体激动剂利拉鲁肽被批准与口服抗糖尿病药物联合用于 2 型糖尿病患者。本文总结了评估利拉鲁肽与一种或两种口服抗糖尿病药物联合使用的疗效、安全性和耐受性的临床试验结果,并与艾塞那肽和二肽基肽酶(DPP-4)抑制剂的作用进行了对比。当与一种或两种口服抗糖尿病药物联合使用时,GLP-1 受体激动剂可有效控制血糖,在某些患者中还可能带来体重减轻和血压降低的整体获益。这些药物具有良好的耐受性;最常见的不良反应是轻度至中度胃肠道症状,通常是短暂的。这些试验中的低血糖发生率较低,但与磺酰脲类药物联合使用时发生率较高。虽然还需要进一步研究,但 GLP-1 受体激动剂可能比其他糖尿病治疗方法具有重要优势,包括 DPP-4 抑制剂。