Are Sulfonylureas Less Desirable Than DPP-4 Inhibitors as Add-on to Metformin in the Treatment of Type 2 Diabetes?

被引:18
作者
Ahren, Bo [1 ]
机构
[1] Lund Univ, Dept Clin Sci Lund, SE-22184 Lund, Sweden
基金
瑞典研究理事会;
关键词
Diabetes; Hyperglycemia; Sulfonylureas; Glimepiride; Glipizide; DPP-4; inhibitors; Vildagliptin; Sitagliptin; Saxagliptin; Islet function; Insulin secretion; Glucagon secretion; Hypoglycemia; Safety; Durability; Comparison; DIPEPTIDYL PEPTIDASE-4 INHIBITORS; BETA-CELL APOPTOSIS; EFFICACY; VILDAGLIPTIN; SITAGLIPTIN; MELLITUS; SAFETY; MANAGEMENT; GLIPIZIDE; COMPLICATIONS;
D O I
10.1007/s11892-011-0179-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sulfonylureas (SUs) are commonly used as add-on to metformin in treatment of type 2 diabetes in patients who are insufficiently controlled by metformin alone. They have good efficacy and have been shown to prevent microvascular complications. However, treatment with SUs is also associated with a high frequency of hypoglycemia, increased body weight, and a high risk of secondary failure. During recent years, dipeptidyl peptidase-4 (DPP-4) inhibitors have emerged as alternatives to SUs. They show similar efficacy as SUs but with lower risk of hypoglycemia, and reduction or no change in body weight, and if confirmed in humans, they may preserve islet function and thereby minimize the risk for secondary failure. Their limitation at present is the lack of long-term (> 5 years) experience on durability and safety. Overall, therefore, the conclusion emerges that SUs are less desirable than DPP-4 inhibitors in management of hyperglycemia in type 2 diabetes.
引用
收藏
页码:83 / 90
页数:8
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