A GLP-1 receptor agonist approved for type 2 diabetes and chronic weight management.
American health & drug benefits|2017|Tran K et al.|78 citations
BACKGROUND: It is estimated that 29.1 million people or 9.3% of the US population have diabetes, which contributes to considerable medical and financial burden. Type 2 diabetes mellitus is characterized by insulin resistance and insulin secretion imp…
PMID: 28794822
The American journal of cardiology|2017|Thrasher J|55 citations
Choices for the treatment of type 2 diabetes mellitus (T2DM) have multiplied as our understanding of the underlying pathophysiologic defects has evolved. Treatment should target multiple defects in T2DM and follow a patient-centered approach that con…
Review
PMID: 28606343
World journal of diabetes|2017|Avgerinos K, Tziomalos K|3 citations
Diabetes mellitus (DM) is a major risk factor for cardiovascular events, including ischemic stroke. Moreover, ischemic stroke appears to be more severe in these patients and to be associated with less favorable outcomes. However, strict glycemic cont…
Review
PMID: 28694927
BMJ (Clinical research ed.)|2017|Hawkes N|1 citation
PMID: 29092887
Current diabetes reports|2017|Herbst R et al.|3 citations
PURPOSE OF REVIEW: Seven trials of new agents to treat type 2 diabetes (T2DM) have been performed to assess cardiovascular (CV) safety. A significant amount of information regarding the effects of drugs in three classes is available, with new data fr…
Review
PMID: 28726152
The lancet. Diabetes & endocrinology|2017|Sorli C et al.|554 citations
BACKGROUND: Despite a broad range of pharmacological options for the treatment of type 2 diabetes, optimum glycaemic control remains challenging for many patients and new therapies are necessary. Semaglutide is a glucagon-like peptide-1 (GLP-1) analo…
Randomized Controlled Trial
PMID: 28110911
Diabetes care|2017|Kaul S|44 citations
The U.S. Food and Drug Administration (FDA) issued a diabetes guidance in 2008 mandating that all new antidiabetes drugs rule out excess cardiovascular (CV) risk, defined as an upper bound of the two-sided 95% CI for major adverse CV events (MACE) of…
Review
PMID: 28637887
PloS one|2017|Peterson R et al.|29 citations
UNLABELLED: The FATZO/Pco mouse is the result of a cross of the C57BL/6J and AKR/J strains. The crossing of these two strains and the selective inbreeding for obesity, insulin resistance and hyperglycemia has resulted in an inbred strain exhibiting o…
Animal Study
PMID: 28640857
The New England journal of medicine|2017|Williams T, Stewart E|13 citations
PMID: 28249136
Journal of endocrinological investigation|2017|Monami M et al.|53 citations
BACKGROUND: The pharmacological stimulation of GLP-1 receptors is associated with an increase in heart rate. A pooled analysis of patient-level data from phase III trials with albiglutide revealed a significant increase in the risk of atrial fibrilla…
ReviewMeta-Analysis
PMID: 28569363
Journal of the American College of Cardiology|2017|Sattar N et al.|65 citations
Recently, treatment with 2 newer classes of type 2 diabetes drugs were found to reduce events in patients with diabetes and cardiovascular (CV) disease, a group common in cardiology clinics. The sodium-glucose cotransporter 2 inhibitor, empagliflozin…
Review
PMID: 28545639
American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists|2017|LeBras M, Barry A, Koshman S|5 citations
PURPOSE: The cardiovascular safety outcomes of newer antidiabetic agents were reviewed. SUMMARY: Seven randomized, placebo-controlled trials involving patients with type 2 diabetes mellitus with or at risk for cardiovascular disease were reviewed. Th…
Review
PMID: 28483748
Circulation|2017|Nauck M et al.|419 citations
Potentiation of glucagon-like peptide-1 (GLP-1) action through selective GLP-1 receptor (GLP-1R) agonism or by prevention of enzymatic degradation by inhibition of dipeptidyl peptidase-4 (DPP-4) promotes glycemic reduction for the treatment of type 2…
Review
PMID: 28847797
Trends in cardiovascular medicine|2017|Secrest M, Udell J, Filion K|31 citations
In this paper, we review the results of large, double-blind, placebo-controlled randomized trials mandated by the US Food and Drug Administration to examine the cardiovascular safety of newly-approved antihyperglycemic agents in patients with type 2…
Review
PMID: 28291655
Diabetes & metabolism journal|2017|Kim H et al.|6 citations
The glucagon-like peptide-1 receptor agonists (GLP-1RAs) were recommended as a monotherapy or combination therapy with oral hypoglycemic agents or basal insulin in the position statement of the Korean Diabetes Association 2017 for pharmacological the…
Review
PMID: 29272081
American journal of cardiovascular drugs : drugs, devices, and other interventions|2017|Chawla H, Tandon N|5 citations
In view of the significant cardiovascular (CV) morbidity and mortality in patients with type 2 diabetes mellitus, and concerns raised about the CV safety of some glucose-lowering drugs, the US Food and Drug Administration (FDA) issued guidance for th…
Review
PMID: 28197977
The lancet. Diabetes & endocrinology|2017|Aroda V et al.|350 citations
BACKGROUND: Several pharmacological treatment options are available for type 2 diabetes; however, many patients do not achieve optimum glycaemic control and therefore new therapies are necessary. We assessed the efficacy and safety of semaglutide, a…
Randomized Controlled Trial
PMID: 28344112
International journal of cardiology|2017|Luconi M et al.|18 citations
Recently, cardiovascular outcome trials with glucose-lowering drugs used in type 2 diabetes mellitus, namely glucagon-like peptide-1 receptor agonists (GLP-1RA), liraglutide and semaglutide, showed a reduction in cardiovascular events, which had not…
Review
PMID: 28285800
Expert review of clinical pharmacology|2017|Scheen A|11 citations
Novelties in the management of type 2 diabetes are dominated by the commercialisation of new glucose-lowering agents, which offer alternatives to older antidiabetic medications, and by the publication of several prospective placebo-controlled outcome…
Review
PMID: 28879786
Diabetes research and clinical practice|2017|Scheen A|13 citations
Dipeptidyl peptidase-4 inhibitors (DPP-4is) and glucagon-like peptide-1 receptor agonists (GLP-1RAs) represent two distinct classes of incretin-based therapies used for the treatment of type 2 diabetes. Non-inferiority versus placebo was shown in lar…
Review
PMID: 28402902