Incretin-based therapy: how do incretin mimetics and DPP-4 inhibitors fit into treatment algorithms for type 2 diabetic patients?

被引:16
|
作者
Nauck, M. [1 ]
Smith, U. [2 ]
机构
[1] Diabet Zentrum Bad Lauterberg, D-37431 Bad Lauterberg im Harz, Germany
[2] Univ Gothenburg, Dept Internal Med, Gothenburg, Sweden
关键词
oral anti-diabetic drugs; incretin-based antidiabetic medication; GLP-1 receptor agonists; incretin mimetics; DPP-4; inhibitors; incretin enhancers; GLUCAGON-LIKE PEPTIDE-1; DIPEPTIDYL PEPTIDASE-4 INHIBITOR; BETA-CELL MASS; METFORMIN-TREATED PATIENTS; IMPROVES GLYCEMIC CONTROL; BLOOD-GLUCOSE CONTROL; EXENATIDE EXENDIN-4; INSULIN GLARGINE; RENAL-INSUFFICIENCY; MILD HYPERGLYCEMIA;
D O I
10.1016/j.beem.2009.03.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Incretin-based antidiabetic medications have been approved for clinical use for approximately two to three years. While their major clinical characteristics have been known from clinical trials, the discussion now focuses on the best clinical use of GLP-1 receptor agonists (incretin mimetics) and inhibitors of the protease dipeptidyl peptidase-4 (DPP-4). Any novel drug will not fully disclose its spectrum of beneficial and adverse activity before long-term trials with clinical endpoints are available. This, typically, will last 5-8 years. Nevertheless, there are convincing reasons to use incretin mimetics and DPP-4 inhibitors even in the absence of such results. This decision should be based on specific patient characteristics and (expected) treatment results, in comparison to other available treatment options. The present manuscript tries to describe the current state-of-the-art of using incretin mimetics and DPP-4 inhibitors in clinical practice, including an attempt to suggest their place in treatment algorithms for type 2-diabetic patients. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:513 / 523
页数:11
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