Heart failure in diabetes: effects of anti-hyperglycaemic drug therapy

被引:426
作者
Gilbert, Richard E. [1 ]
Krum, Henry [2 ]
机构
[1] Univ Toronto, Div Endocrinol, St Michaels Hosp, Toronto, ON M5S 1A1, Canada
[2] Monash Univ, Ctr Cardiovasc Res & Educ Therapeut, Melbourne, Vic 3004, Australia
关键词
ACUTE MYOCARDIAL-INFARCTION; LEFT-VENTRICULAR DYSFUNCTION; ENDOTHELIAL GROWTH-FACTOR; CARDIOVASCULAR-DISEASE; PEPTIDE-1; INFUSION; EJECTION FRACTION; SODIUM RETENTION; RENAL SODIUM; INSULIN; MORTALITY;
D O I
10.1016/S0140-6736(14)61402-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Individuals with diabetes are not only at high risk of developing heart failure but are also at increased risk of dying from it. Fortunately, antiheart failure therapies such as angiotensin-converting-enzyme inhibitors, beta blockers and mineralocorticoid-receptor antagonists work similarly well in individuals with diabetes as in individuals without the disease. Response to intensive glycaemic control and the various classes of antihyperglycaemic agent therapy is substantially less well understood. Insulin, for example, induces sodium retention and thiazolidinediones increase the risk of heart failure. The need for new glucose-lowering drugs to show cardiovascular safety has led to the unexpected finding of an increase in the risk of admission to hospital for heart failure in patients treated with the dipeptidylpeptidase-4 (DPP4) inhibitor, saxagliptin, compared with placebo. Here we review the relation between glycaemic control and heart failure risk, focusing on the state of knowledge for the various types of antihyperglycaemic drugs that are used at present.
引用
收藏
页码:2107 / 2117
页数:11
相关论文
共 104 条
[1]   Effect of diabetes mellitus on formation of coronary collateral vessels [J].
Abaci, A ;
Oguzhan, A ;
Kahraman, S ;
Eryol, NK ;
Ünal, S ;
Arinç, H ;
Ergin, A .
CIRCULATION, 1999, 99 (17) :2239-2242
[2]  
[Anonymous], ENDOCRINOLOGIC METAB
[3]  
[Anonymous], NEW ENGL J MED
[4]  
[Anonymous], EUR HEART FAIL C
[5]  
[Anonymous], ASS REP AV
[6]  
[Anonymous], 1928, JAMA
[7]  
[Anonymous], 52 WEEK DOUBL BLIND
[8]   SGLT1, a novel cardiac glucose transporter, mediates increased glucose uptake in PRKAG2 cardiomyopathy [J].
Banerjee, Sanjay K. ;
Wang, David W. ;
Alzamora, Rodrigo ;
Huang, Xueyin N. ;
Pastor-Soler, Nuria M. ;
Hallows, Kenneth R. ;
McGaffin, Kenneth R. ;
Ahmad, Ferhaan .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2010, 49 (04) :683-692
[9]   SGLT1 is a novel cardiac glucose transporter that is perturbed in disease states [J].
Banerjee, Sanjay K. ;
McGaffin, Kenneth R. ;
Pastor-Soler, Nuria M. ;
Ahmad, Ferhaan .
CARDIOVASCULAR RESEARCH, 2009, 84 (01) :111-118
[10]   Effects of pioglitazone versus glipizide on body fat distribution, body water content, and hemodynamics in type 2 diabetes [J].
Basu, A ;
Jensen, MD ;
McCann, F ;
Mukhopadhyay, D ;
Joyner, MJ ;
Rizza, RA .
DIABETES CARE, 2006, 29 (03) :510-514