Insulin plus incretin: A glucose-lowering strategy for type 2-diabetes

被引:40
作者
Ahren, Bo [1 ]
机构
[1] Lund Univ, Dept Clin Sci Lund, B11 BMC, S-22184 Lund, Sweden
关键词
Type; 2; diabetes; Glucose lowering; Insulin therapy; Glucagon-like peptide-1 receptor agonists; Dipeptidyl peptidase-4 inhibitors; Incretin therapy; Combination;
D O I
10.4239/wjd.v5.i1.40
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There are many advantages of combining incretin therapy [glucagon-like peptide-1 (GLP-1) receptor agonists and dipeptidyl peptidase-4 (DPP-4) inhibitors] with insulin therapy as a glucose-lowering strategy in type 2 diabetes. One important advantage is the complementary mode of the mechanistic action of incretin and insulin therapy. Another advantage is the reduction in risk of hypoglycemia and weight gain when adding incretin therapy to insulin. Several clinical trials have studied the addition of GLP-1 receptor agonists [exena-tide BID (twice daily), lixisenatide, albiglutide] or DPP-4 inhibitors (vildagliptin, sitagliptin, saxagliptin, alogliptin, linagliptin) to ongoing insulin therapy or adding insulin to ongoing therapy with a GLP-1 receptor agonist (liraglutide). These studies show improved glycemia in the presence of limited risk for hypoglycemia and weight gain with the combination of incretin therapy with insulin. This article reviews the background and clinical studies on this combination. (C) 2014 Baishideng Publishing Group Co., Limited. All rights reserved.
引用
收藏
页码:40 / 51
页数:12
相关论文
共 85 条
[1]   Inhibition of dipeptidyl peptidase-4 reduces glycemia, sustains insulin levels, and reduces glucagon levels in type 2 diabetes [J].
Ahrén, B ;
Landin-Olsson, M ;
Jansson, PA ;
Svensson, M ;
Holmes, D ;
Schweizer, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (05) :2078-2084
[2]  
Ahren B, 2013, DIABETOLOGIA, V56, pS51
[3]   β- and α-Cell Dysfunction in Subjects Developing Impaired Glucose Tolerance Outcome of a 12-Year Prospective Study in Postmenopausal Caucasian Women [J].
Ahren, B. .
DIABETES, 2009, 58 (03) :726-731
[4]  
Ahren B, 2013, J EUR DIABET NURSING, V10, P31, DOI DOI 10.1002/EDN.221]
[5]   Dipeptidyl peptidase-4 inhibitors -: Clinical data and clinical implications [J].
Ahren, Bo .
DIABETES CARE, 2007, 30 (06) :1344-1350
[6]   Avoiding hypoglycemia: a key to success for glucose-lowering therapy in type 2 diabetes [J].
Ahren, Bo .
VASCULAR HEALTH AND RISK MANAGEMENT, 2013, 9 :155-163
[7]  
Ahren B, 2010, VITAM HORM, V84, P203, DOI [10.1016/S0083-6729(10)84011-7, 10.1016/B978-0-12-381517-0.00007-2]
[8]   Vildagliptin Enhances Islet Responsiveness to Both Hyper- and Hypoglycemia in Patients with Type 2 Diabetes [J].
Ahren, Bo ;
Schweizer, Anja ;
Dejager, Sylvie ;
Dunning, Beth E. ;
Nilsson, Peter M. ;
Persson, Margaretha ;
Foley, James E. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2009, 94 (04) :1236-1243
[9]   A meta-analysis of serious adverse events reported with exenatide and liraglutide: Acute pancreatitis and cancer [J].
Alves, Carlos ;
Batel-Marques, Francisco ;
Macedo, Ana F. .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2012, 98 (02) :271-284
[10]   The dipeptidyl peptidase IV inhibitor vildagliptin suppresses endogenous glucose production and enhances islet function after single-dose administration in type 2 diabetic patients [J].
Balas, Bogdan ;
Baig, Muhammad R. ;
Watson, Catherine ;
Dunning, Beth E. ;
Ligueros-Saylan, Monica ;
Wang, Yibin ;
He, Yan-Ling ;
Darland, Celia ;
Holst, Jens J. ;
Deacon, Carolyn F. ;
Cusi, Kenneth ;
Mari, Andrea ;
Foley, James E. ;
DeFronzo, Ralph A. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2007, 92 (04) :1249-1255