PMID- 22422427 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20121002 LR - 20240330 IS - 1869-6961 (Electronic) IS - 1869-6953 (Print) IS - 1869-6961 (Linking) VI - 3 IP - 1 DP - 2012 Nov TI - A review of exenatide: optimizing glycemic control and associated cardiovascular risk factors in type 2 diabetes. PG - 1-16 LID - 10.1007/s13300-012-0003-x [doi] LID - 3 AB - Type 2 diabetes mellitus (T2DM) is a well-recognized risk factor for the development of cardiovascular disease. With an increasing prevalence of obesity, this risk has increased further. Management of T2DM in obese patients is particularly challenging as treatment with the majority of glucose-lowering agents results in weight gain. Thus, the development of a therapeutic option which could improve glycemic control without weight gain or hypoglycemia, such as the glucagon-like peptide-1 (GLP-1) analog exenatide, is a welcome addition to the currently available therapies in the management of T2DM. With recognition and better understanding of the role of incretin hormones in T2DM, exenatide was developed and introduced into clinical practice in 2005. Both randomized controlled trials and retrospective observational studies have shown that treatment with exenatide not only improves glycemic control, with a low risk of hypoglycemia, but also results in concurrent weight loss and the additional benefit of improvement in cardiovascular risk factors. This article will provide an overview of both short- and long-acting exenatide in the management of T2DM and associated cardiovascular risk factors. FAU - Htike, Zin Z AU - Htike ZZ AD - Department of Diabetes and Endocrinology, Leicester Royal Infirmary, University Hospitals of Leicester NHS Trust, Leicester, UK. FAU - Khunti, Kamlesh AU - Khunti K FAU - Davies, Melanie AU - Davies M LA - eng PT - Journal Article DEP - 20120316 PL - United States TA - Diabetes Ther JT - Diabetes therapy : research, treatment and education of diabetes and related disorders JID - 101539025 PMC - PMC3508112 EDAT- 2012/03/17 06:00 MHDA- 2012/03/17 06:01 PMCR- 2012/03/16 CRDT- 2012/03/17 06:00 PHST- 2011/12/02 00:00 [received] PHST- 2012/03/17 06:00 [entrez] PHST- 2012/03/17 06:00 [pubmed] PHST- 2012/03/17 06:01 [medline] PHST- 2012/03/16 00:00 [pmc-release] AID - 3 [pii] AID - 10.1007/s13300-012-0003-x [doi] PST - ppublish SO - Diabetes Ther. 2012 Nov;3(1):1-16. doi: 10.1007/s13300-012-0003-x. Epub 2012 Mar 16.