Recent advances in incretin-based therapies

被引:67
作者
Russell-Jones, David [1 ,2 ]
Gough, Stephen [3 ,4 ]
机构
[1] Royal Surrey Cty Hosp, Cedar Ctr, Guildford GU2 7XX, Surrey, England
[2] Univ Surrey, Guildford GU2 5XH, Surrey, England
[3] Churchill Hosp, Oxford Ctr Diabet Endocrinol & Metab, Oxford OX3 7LJ, England
[4] NIHR Oxford Biomed Res Ctr, Oxford, England
关键词
GLUCAGON-LIKE PEPTIDE-1; IMPROVES GLYCEMIC CONTROL; PEPTIDASE-4 INHIBITOR SITAGLIPTIN; TWICE-DAILY EXENATIDE; DRUG-NAIVE PATIENTS; HUMAN GLP-1 ANALOG; DOUBLE-BLIND; INSULIN GLARGINE; TREATED PATIENTS; OPEN-LABEL;
D O I
10.1111/j.1365-2265.2012.04483.x
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The global burden of type 2 diabetes is growing. Traditional therapies are suboptimal and there is a clear unmet need for treatments that offer effective glucose control while addressing the comorbid factors associated with diabetes, such as obesity and risk of cardiovascular disease, without the fear of hypoglycaemia. Glucagon-like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors offer a novel way of reducing hyperglycaemia by targeting the incretin system. This review provides an overview of the development of incretin-based therapies and explains their differing modes of action compared with traditional interventions. A comparison of the clinical profiles of current glucagon-like peptide-1 receptor agonists [liraglutide and exenatide (twice-daily and once-weekly)] and dipeptidyl peptidase-4 inhibitors (sitagliptin, saxagliptin, vildagliptin and linagliptin) is performed alongside a discussion of the placement of incretin-based therapies in treatment guidelines. Further improvements in this class are expected, and we will examine some of the novel glucagon-like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors currently under development.
引用
收藏
页码:489 / 499
页数:11
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