Safety of dipeptidyl peptidase-4 inhibitors for treating type 2 diabetes

被引:118
|
作者
Scheen, Andre J. [1 ,2 ]
机构
[1] Univ Liege, CHU Sart Tilman, Dept Med, Div Diabet Nutr & Metab Disorders, B-4000 Liege 1, Belgium
[2] Univ Liege, CHU Sart Tilman, CIRM, Div Clin Pharmacol, Liege, Belgium
关键词
cardiovascular outcome; dipeptidyl peptidase-4 inhibitor; heart failure; pancreas; safety; special population; type 2 diabetes mellitus; IMPROVES GLYCEMIC CONTROL; INCRETIN-BASED DRUGS; CARDIOVASCULAR OUTCOME TRIALS; RANDOMIZED CONTROLLED-TRIALS; SEVERE RENAL IMPAIRMENT; SAVOR-TIMI; 53; POOLED ANALYSIS; DOUBLE-BLIND; ACUTE-PANCREATITIS; HEART-FAILURE;
D O I
10.1517/14740338.2015.1006625
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Dipeptidyl peptidase-4 (DPP-4) inhibitors (gliptins) occupy a growing place in the armamentarium of drugs used for the management of hyperglycemia in type 2 diabetes, although some safety concerns have been raised in recent years. Areas covered: An updated review providing an analysis of available safety data (meta-analyses, randomized controlled trials, observational cohort and case-control studies and pharmacovigilance reports) with five commercialized DPP-4 inhibitors (sitagliptin, vildagliptin, saxagliptin, alogliptin, linagliptin). A special focus is given to overall safety profile; pancreatic adverse events (AEs) (acute pancreatitis, pancreatic cancer); overall cardiovascular safety (myocardial infarction and stroke); congestive heart failure concern and finally, safety in special populations (elderly, renal impairment). Expert opinion: The good tolerance/safety profile of DPP-4 inhibitors has been largely confirmed, including in more fragile populations (elderly, renal impairment) with almost no increased risk of infection or gastrointestinal AEs, no weight gain and a minimal risk of hypoglycemia. Although an increased risk of acute pancreatitis and pancreatic cancer was suspected, the complete set of available data appears reassuring so far. Cardiovascular safety of DPP-4 inhibitors has been proven but an unexpected increased risk of heart failure has been reported which should be confirmed in ongoing trials and better understood. Further postmarketing surveillance is recommended.
引用
收藏
页码:505 / 524
页数:20
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