Gliptins: a new class of oral hypoglycaemic agent

被引:27
作者
Chahal, H. [1 ]
Chowdhury, T. A. [1 ]
机构
[1] Royal London Hosp, Dept Diabet & Meetabol, London E1 1BB, England
关键词
DIPEPTIDYL-PEPTIDASE-IV; IMPROVED GLUCOSE-TOLERANCE; IMPROVES GLYCEMIC CONTROL; TYPE-2; DIABETES-MELLITUS; GLUCAGON-LIKE PEPTIDE-1; DRUG-NAIVE PATIENTS; INHIBITOR SITAGLIPTIN; DOUBLE-BLIND; TREATED PATIENTS; FATTY RATS;
D O I
10.1093/qjmed/hcm081
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The epidemic of type 2 diabetes worldwide continues unabated. Despite a number of existing therapies, treatment goals are seldom fully achieved. While insulin resistance and beta cell failure remain important in the pathogenesis of the condition, the role of incretin hormones in glucose homeostasis has recently become clearer. Incretins have several glucoregulatory mechanisms, and a novel approach to the treatment of type 2 diabetes focuses on enhancing and prolonging the physiological actions of these hormones. Gliptins inhibit the enzyme dipeptidyl peptidase-IV (DPP-IV), which degrades incretin hormones. These drugs are a promising new class of oral hypoglycaemic medication, which appear to be weight-neutral and have few side-effects, although the published clinical studies are mainly regulatory licensing studies. As these drugs now are available for clinical use, we discuss the mechanism of action, efficacy and potential adverse effects of this new class of oral hypoglycaemic agent.
引用
收藏
页码:671 / 677
页数:7
相关论文
共 36 条
[21]   INCRETIN EFFECTS OF INCREASING GLUCOSE LOADS IN MAN CALCULATED FROM VENOUS INSULIN AND C-PEPTIDE RESPONSES [J].
NAUCK, MA ;
HOMBERGER, E ;
SIEGEL, EG ;
ALLEN, RC ;
EATON, RP ;
EBERT, R ;
CREUTZFELDT, W .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1986, 63 (02) :492-498
[22]   Effect of rosiglitazone on the risk of myocardial infarction and death from cardiovascular causes (vol 356, pg 2457, 2007) [J].
Nissen, Steven E. ;
Wolski, Kathy .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 356 (24) :2457-2471
[23]   Improved glucose tolerance in Zucker fatty rats by oral administration of the dipeptidyl peptidase IV inhibitor isoleucine thiazolidide [J].
Pederson, RA ;
White, HA ;
Schlenzig, D ;
Pauly, RP ;
McIntosh, CHS ;
Demuth, HU .
DIABETES, 1998, 47 (08) :1253-1258
[24]   Efficacy and tolerability of vildagliptin monotherapy in drug-naive patients with type 2 diabetes [J].
Pi-Sunyer, F. Xavier ;
Schweizer, Anja ;
Mills, David ;
Dejager, Sylvie .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2007, 76 (01) :132-138
[25]   Long-term treatment with dipeptidyl peptidase IV inhibitor improves hepatic and peripheral insulin sensitivity in the VDF Zucker rat - A euglycemic-hyperinsulinemic clamp study [J].
Pospisilik, JA ;
Stafford, SG ;
Demuth, HU ;
McIntosh, CHS ;
Pederson, RA .
DIABETES, 2002, 51 (09) :2677-2683
[26]   Twelve-week monotherapy with the DPP-4 inhibitor vildagliptin improves glycemic control in subjects with type 2 diabetes [J].
Pratley, R. E. ;
Jauffret-Kamel, S. ;
Galbreath, E. ;
Holmes, D. .
HORMONE AND METABOLIC RESEARCH, 2006, 38 (06) :423-428
[27]   Efficacy and safety of the dipeptidyl peptidase-4 inhibitor sitagliptin as monotherapy in patients with type 2 diabetes mellitus [J].
Raz, I. ;
Hanefeld, M. ;
Xu, L. ;
Caria, C. ;
Williams-Herman, D. ;
Khatami, H. .
DIABETOLOGIA, 2006, 49 (11) :2564-2571
[28]   Long-term inhibition of dipeptidyl peptidase IV improves glucose tolerance and preserves islet function in mice [J].
Reimer, MK ;
Holst, JJ ;
Ahrén, B .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2002, 146 (05) :717-727
[29]   Improved glycaemic control with dipeptidyl peptidase-4 inhibition in patients with type 2 diabetes: vildagliptin (LAF237) dose response [J].
Ristic, S ;
Byiers, S ;
Foley, J ;
Holmes, D .
DIABETES OBESITY & METABOLISM, 2005, 7 (06) :692-698
[30]   Efficacy and tolerability of initial combination therapy with vildagliptin and pioglitazone compared with component monotherapy in patients with type 2 diabetes [J].
Rosenstock, J. ;
Baron, M. A. ;
Camisasca, R. -P. ;
Cressier, F. ;
Couturier, A. ;
Dejager, S. .
DIABETES OBESITY & METABOLISM, 2007, 9 (02) :175-185