Emerging GLP-1 receptor agonists

被引:23
|
作者
Lund, Asger [1 ]
Knop, Filip K. [1 ]
Vilsboll, Tina [1 ]
机构
[1] Univ Copenhagen, Gentofte Hosp, Dept Internal Med F, Diabet Res Div, DK-2900 Hellerup, Denmark
关键词
albiglutide; CJC-1134-PC; dulaglutide; exenatide; exenatide once-weekly; glucagon-like peptide-1 receptor agonists; liraglutide; lixisenatide; semaglutide; type; 2; diabetes; GLUCAGON-LIKE PEPTIDE-1; AMERICAN-DIABETES-ASSOCIATION; GLYCEMIC CONTROL; EXENATIDE EXENDIN-4; DOUBLE-BLIND; OPEN-LABEL; EUROPEAN-ASSOCIATION; CONSENSUS STATEMENT; INSULIN-SECRETION; TREATED PATIENTS;
D O I
10.1517/14728214.2011.616493
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Recently, glucagon-like peptide-1 receptor (GLP-1R) agonists have become available for the treatment of type 2 diabetes. These agents exploit the physiological effects of GLP-1, which is able to address several of the pathophysiological features of type 2 diabetes. GLP-1R agonists presently available are administered once or twice daily, but several once-weekly GLP-1R agonists are in late clinical development. Areas covered: The present review aims to give an overview of the clinical data on the currently available GLP-1R agonists used for treatment of type 2 diabetes, exenatide and liraglutide, as well as the emerging GLP-1R agonists including the long-acting compounds. Expert opinion: An emerging therapeutic trend toward initial or early combination therapy with metformin-and incretin-based therapy is anticipated for patients with type 2 diabetes. GLP-1-based therapy has so far proven safe and tolerable. The determination of which incretin-based therapy to choose necessitates comparisons between the various GLP-1R agonists. The available GLP-1R agonists cause sustained weight loss and clinical relevant improvement of glycemic control. The long-acting GLP-1R agonists in late development may improve the effects of GLP-1 even further with optimized pharmacokinetic profiles resulting in fewer side effects. Meta-analyses have shown promising effects on cardiovascular disease and data from ongoing multicenter trials with cardiovascular endpoints are expected in 2015.
引用
收藏
页码:607 / 618
页数:12
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