Combining Basal Insulin Analogs with Glucagon-Like Peptide-1 Mimetics

被引:16
|
作者
Perfetti, Riccardo [1 ]
机构
[1] Sanofi Aventis, F-75013 Paris, France
关键词
FASTING PLASMA-GLUCOSE; QUALITY-OF-LIFE; GLYCEMIC CONTROL; ORAL-AGENTS; NPH INSULIN; TYPE-2; GLARGINE; EXENATIDE; THERAPY; TRIAL;
D O I
10.1089/dia.2010.0250
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Basal insulin analogs are recognized as an effective method of achieving and maintaining glycemic control for patients with type 2 diabetes. However, the progressive nature of the disease means that some individuals may require additional ways to maintain their glycemic goals. Intensification in these circumstances has traditionally been achieved by the addition of short-acting insulin to cover postprandial glucose excursions that are not targeted by basal insulin. However, intensive insulin regimens are associated with a higher risk of hypoglycemia and weight gain, which can contribute to a greater burden on patients. The combination of basal insulin with a glucagon-like peptide-1 (GLP-1) mimetic is a potentially attractive solution to this problem for some patients with type 2 diabetes. GLP-1 mimetics target postprandial glucose and should complement the activity of basal insulins; they are also associated with a relatively low risk of associated hypoglycemia and moderate, but significant, weight loss. Although the combination has not been approved by regulatory authorities, preliminary evidence from mostly small-scale studies suggests that basal insulins in combination with GLP-1 mimetics do provide improvements in A1c and postprandial glucose with concomitant weight loss and no marked increase in the risk of hypoglycemia. These results are promising, but further studies are required, including comparisons with basal-bolus therapy, before the complex value of this association can be fully appreciated.
引用
收藏
页码:873 / 881
页数:9
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