Dipeptidyl Peptidase-4 Inhibitors and Their Effects on the Cardiovascular System

被引:9
作者
Solun, B. [1 ,2 ]
Marcoviciu, D. [1 ,2 ]
Dicker, D. [1 ,2 ]
机构
[1] Hasharon Hosp, Rabin Med Ctr, Dept Internal Med D, IL-49100 Petah Tiqwa, Israel
[2] Hasharon Hosp, Rabin Med Ctr, Multidisciplinary Obes Clin, IL-49100 Petah Tiqwa, Israel
关键词
Dipeptidyl peptidase 4; Incretin; Cardiovascular disease; Type 2 diabetes mellitus; GLUCAGON-LIKE PEPTIDE-1; TYPE-2; DIABETES-MELLITUS; ISCHEMIA-REPERFUSION INJURY; MYOCARDIAL-INFARCTION; SITAGLIPTIN IMPROVES; ENDOTHELIAL FUNCTION; INSULIN-SECRETION; DPP-4; INHIBITION; BLOOD-PRESSURE; INCRETIN;
D O I
10.1007/s11886-013-0382-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It is well known that patients with type 2 diabetes mellitus (T2DM) are at increased risk of cardiovascular (CV) disease. Elevated plasma glucose levels that independently lead to increased cardiovascular risk, combined with associated co-morbidities such as obesity, hypertension, and dyslipidemia, further contribute to the development of CV complications. Dipeptidyl peptidase 4 inhibitors (DPP-4 inhibitors) are a relatively new class of drugs used for the treatment of diabetes and recently have been widely used in clinical practice. They exert their actions through degradation inhibition of endogenous glucagon-like peptides (GLP-1) and glucose-dependent insulinotropic peptides (GIP), with a resulting increase in glucose mediated insulin secretion and a suppression of glucagon secretion. Since GLP-1 is known to have an impact not only on plasma glucose levels but also to have cardiovascular protective effects there is increased speculation of whether DPP-4 inhibitors will have similar effects. Though many short-term studies have been encouraging, ongoing long-term clinical trials on humans are needed to provide further clarity to the complete safety profiles of these agents in terms of cardiovascular risk, and whether they may exert potential cardiovascular benefit. This review includes available data on the cardiovascular effects of DPP-4 inhibitors as well as their overall safety profile.
引用
收藏
页数:8
相关论文
共 62 条
[1]   The Extrapancreatic Effects of Glucagon-Like Peptide-1 and Related Peptides [J].
Abu-Hamdah, Rania ;
Rabiee, Atoosa ;
Meneilly, Graydon S. ;
Shannon, Richard P. ;
Andersen, Dana K. ;
Elahi, Dariush .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2009, 94 (06) :1843-1852
[2]  
[Anonymous], ENDOCR PRACT S1
[3]  
[Anonymous], 2009, International Journal of Drug Development Research
[4]   Effect of stromal-cell-derived factor 1 on stem-cell homing and tissue regeneration in ischaemic cardiomyopathy [J].
Askari, AT ;
Unzek, S ;
Popovic, ZB ;
Goldman, CK ;
Forudi, F ;
Kiedrowski, M ;
Rovner, A ;
Ellis, SG ;
Thomas, JD ;
DiCorleto, PE ;
Topol, EJ ;
Penn, MS .
LANCET, 2003, 362 (9385) :697-703
[5]   Pharmacology of Dipeptidyl Peptidase-4 Inhibitors Similarities and Differences [J].
Baetta, Roberta ;
Corsini, Alberto .
DRUGS, 2011, 71 (11) :1441-1467
[6]  
Bayliss WM, 1906, BIOCHEM J, V1, P28
[7]  
Bethel M. A., 2009, 69 SCI SESS AM DIAB
[8]   Glucagon-like peptide 1 can directly protect the heart against ischemia/reperfusion injury [J].
Bose, AK ;
Mocanu, MM ;
Carr, RD ;
Brand, CL ;
Yellon, DM .
DIABETES, 2005, 54 (01) :146-151
[9]   Sitagliptin promotes macrophage-to-faeces reverse cholesterol transport through reduced intestinal cholesterol absorption in obese insulin resistant CETP-apoB100 transgenic mice [J].
Briand, F. ;
Thieblemont, Q. ;
Burcelin, R. ;
Sulpice, T. .
DIABETES OBESITY & METABOLISM, 2012, 14 (07) :662-665
[10]   Pancreatic α-cell dysfunction in diabetes [J].
Burcelin, R. ;
Knauf, C. ;
Cani, P. D. .
DIABETES & METABOLISM, 2008, 34 :S49-S55