Clinical results of treating type 2 diabetic patients with sitagliptin, vildagliptin or saxagliptin - diabetes control and potential adverse events

被引:85
作者
Ahren, Bo [1 ]
机构
[1] Lund Univ, Dept Clin Sci, Lund, Sweden
关键词
glucagon-like peptide-1; dipeptidyl peptidase-4; type; 2; diabetes; sitagliptin; vildagliptin; treatment; DIPEPTIDYL PEPTIDASE-4 INHIBITOR; DRUG-NAIVE PATIENTS; GLUCAGON-LIKE PEPTIDE-1; IMPROVES GLYCEMIC CONTROL; BETA-CELL FUNCTION; ONGOING METFORMIN THERAPY; DOUBLE-BLIND; IV INHIBITOR; RECEPTOR AGONISTS; DPP-4; INHIBITOR;
D O I
10.1016/j.beem.2009.03.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Inhibition of dipeptidyl peptidase-4 (DPP-4) is a novel oral treatment for type 2 diabetes. DPP-4 inhibition increases insulin secretion and reduces glucagon secretion by preventing the inactivation of glucagon-like peptide-1 (GLP-1), thereby lowering glucose levels. Several DPP-4 inhibitors are in clinical development; more Studies exist for sitagliptin and vildagliptin. They improve metabolic control in type 2 diabetes in monotherapy and also in combination with metformin, sulphonylurea and thiazolidinediones. HbA(1c) is reduced by approximately 0.6-1.1% in studies Lip to 52 weeks. Similar, although more limited, results were obtained for saxagliptin. DPP-4 inhibitors are safe and tolerable with no increased risk of adverse events compared to placebo and have a low risk of hypoglycaemia. DPP-4 inhibitors are body weight-neutral. The DPP-4 inhibitors are recommended for use in the early stage of type 2 diabetes, in combination with metformin in subjects with inadequate glycaemic control. DPP-4 inhibition may also be used in combination with sulphonylurea and thiazolidinediones and potentially also in combination with insulin. The durability and long-term safety of DPP-4 inhibitiors remain to be established. (C) 2009 Elsevier Ltd. All rights reserved.
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页码:487 / 498
页数:12
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