Treatment potential of the GLP-1 receptor agonists in type 2 diabetes mellitus: a review

被引:32
|
作者
Ostergaard, L. [1 ]
Frandsen, Christian S. [1 ]
Madsbad, S. [1 ]
机构
[1] Univ Copenhagen, Hvidovre Hosp, Dept Endocrinol, Copenhagen, Denmark
关键词
GLP-1 receptor agonist; dulaglutide; albiglutide; type 2 diabetes mellitus; liraglutide; exenatide; lixisenatide; GLUCAGON-LIKE PEPTIDE-1; PLACEBO-CONTROLLED TRIAL; IMPROVED GLYCEMIC CONTROL; ONCE-DAILY LIXISENATIDE; TWICE-DAILY EXENATIDE; BETA-CELL FUNCTION; METFORMIN-TREATED PATIENTS; BIPHASIC INSULIN ASPART; FIXED-RATIO COMBINATION; DRUG-NAIVE PATIENTS;
D O I
10.1586/17512433.2016.1121808
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Over the last decade, the discovery of glucagon-like peptide 1 receptor agonists (GLP-1 RAs) has increased the treatment options for patients with type 2 diabetes mellitus (T2DM). GLP-1 RAs mimic the effects of native GLP-1, which increases insulin secretion, inhibits glucagon secretion, increases satiety and slows gastric emptying. This review evaluates the phase III trials for all approved GLP-1 RAs and reports that all GLP-1 RAs decrease HbA1c, fasting plasma glucose, and lead to a reduction in body weight in the majority of trials. The most common adverse events are nausea and other gastrointestinal discomfort, while hypoglycaemia is rarely reported when GLP-1 RAs not are combined with sulfonylurea or insulin. Treatment options in the near future will include co-formulations of basal insulin and a GLP-1 RA.
引用
收藏
页码:241 / 265
页数:25
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