Role of Glucagon Analogues in Cardiovascular disease

fictitious character of Glucagon Analogues in Cardiovascular illnessThe Potential Role of Glucagon Like Peptide 1 (GLP-1) Analogues in Cardiovascular diseaseIntroduction batch who have a diagnosis of diabetes have a triple venture of developing cardiovascular disease (CVD) and unfortunately poorer clinical outcomes following myocardial infarction, angioplasty and bypass surgeries (Hausenloy and Yellon 2008). It is estimated that CVD is responsible for 65% of deaths in people with type 2 diabetes (Burge 2012). Management of diabetes includes identifying, preventing and managing CVD riskiness factors such as dyslipidaemia and hypertension (NICE 2014). Other risk factors for CVD include poor or inadequate consumption of fruits and vegetables, smoking, central obesity, psychosocial factors, adapted lipids, inactivity and unsafe alcohol consumption (World Heart Federation 2014 Yusuf et al 2004). GLP-1 analogues indicated to treat diabetes have been shown to have cardiovascular benef its (Hausenloy and Yellon 2008).GLP 1GLP 1 is an incretin by nature occurring in the body and is secreted due to the presence of food in the ileum, change magnitude endogenous insulin, inhibiting glucagon, thereby reducing state of affairs prandial hyperglycaemia and is to a fault responsible for controlling appetite and satiety (Hausenloy and Yellon 2008 Sheikh 2013). GLP -1 does not vitrine hypoglycaemia because its actions argon inhibited when line of credit glucose is fasting levels (Hausenloy and Yellon 2008). GLP- 1 receptors are extensively distributed throughout the body in the brain, lungs, intestines, stomach, pancreas, and heart. GLP-1 itself has a half deportment of 1 2 minutes after secretion (Burge 2012 Zhao 2013). The presence of the receptors in the heart has been the focus of new research.Cardiovascular makeIn animate being studies GLP 1 was seen to cause vasodilation (Brown 2012). An increase in heart invest and extraction pressure were both observ ed in rats that were either conscious or sedated, but there is some controversy with the mechanism (Zhao 2013). When GLP-1 has been inf apply dogs with dilated cardiomyopathy showed better cardiac performance after GLP 1 infusion (Zhao 2013). Left ventricular systolic and diastolic usages were improved after GLP 1 infusion in decompensated heart failure (Zhao 2013).Ban et al (2008) work on black eye heart as cited in Brown (2012) has shown that there are GLP 1 receptors in the endothelium and cardiac myocytes. When GLP 1 was administered during reperfusion studies cardiac prostitute was slight apt(predicate) (Brown 2012).Apart from the animal studies, there have been some kind 2 trials in compassionates with CVD (Zhao 2013). The first investigators to prove that infusing GLP 1 for 3 eld improved global and regional left ventricular w only exertion scores in patients with dysfunction of the left ventricle after myocardial infraction was Shannons group (Zhao 2013). They also concluded that there was minify hospital stay and mortality as an in patient. Several weeks post discharge these effects remained.An experimental study of 14 people with coronary thrombosis artery disease who were toughened with GLP 1 at a vagabond of 1.2pmol/kg/min resulted in improvement of left ventricular function (Zhao 2013). This was corroborated by an opposite study of 172 patients who were do by with exenatide at a rate of 0.12g/min for 6 hours post elevation of ST segment MI.A retrospective study of 420,493 people found that individuals who received treatment with exenatide were less likely to experience cardiovascular event, hospitalization due to CVD or all cause hospitalization when compared to non exenatide treated people even though they were more likely to be obese, have prior CVD, high cholesterol and other co morbidities at baseline (Best et al 2011 Brown 2012).The use of exenatide in patients with type 2 diabetes did not show an increase in cardiova scular disease and similarly liraglutide was not associated with any major adverse cardiac event in an analysis of phase 2 and 3 trials (Sheikh 2013). high blood pressureAnimal studies utilizing GLP 1 have concluded a go down in hypertension development in Dahl salt sensitive rats (Zhao 2013). This decrease in blood pressure was also observed in human trials with the GLP 1 agonists exenatide and liraglutide. A meta analysis of 16 disarrange controlled trials of 5860 people of which 3443 were randomized to a GLP 1 agonist concluded that exenatide and liraglutide caused a fall in systolic and diastolic blood pressure by 1 5 mmHg when compared to other hypoglycaemic medication and placebo in patients with type 2 diabetes (T2DM) (Wang et al 2013). The LEAD trial concluded that liraglutide caused a reduction of systolic blood pressure ranging 3.6 6.7mmHg within 2 weeks of starting therapy (Burge 2012). This effect was seen for the full 26 weeks of the trial.The DURATION trial al so reported reduction in systolic blood pressure (Burge 2012). Data from 6 trial concluded that subjects with T2DM who were treated for 6 months with exenatide saw a significant reduction in systolic blood pressure (Zhao 2013). There is also promising data from phase 3 trials of liraglutide which concluded that there may be reduction in systolic blood pressure when liraglutide is used with other agents such as metformin (Zhao 2013). Exenatide use reportedly cause a fall in systolic blood pressure in obese patients with T2DM who were also treated with insulin (Sheikh 2013). This decrease in systolic blood pressure was confirmed by an analysis of 2171 patients (Sheikh 2013). Liraglutide was also reported to cause a reduction in systolic blood pressure in Asian patients (Sheikh 2013).ConclusionThe data from the use of GLP-1 in both animal and human studies show unchanging reduction in systolic blood pressure a cognize risk factor for both cardiac disease and cerebrovascular chance e vent (CVA). There have also been promising signs that there may be a GLP 1 cardio protective effect post cardiac damage and improvement in left ventricular function. It is not clear whether the doses used to treat diabetes will interpret the same level of reduction in systolic blood pressure and cardiovascular protection in the long-lived term.More clinical studies are required focusing the benefits of GLP-1 analogues on the cardiovascular system as the data will not only provide benefits to patients with T2DM but also patients who are at risk or get under ones skin a CVD.ReferencesBest, J. H., Byron J. Hoogwerf, B. J. and Hussein, M. A. (2011) Risk of Cardiovascular Disease Events in Patients With Type 2 Diabetes Prescribed the Glucagon-Like Peptide 1 (GLP-1) Receptor Agonist Exenatide Twice Daily or Other Glucose-Lowering Therapies, Diabetes Care, 34(1), pp. 90 95. American Diabetes Association. Online. Available at http//www.ncbi.nlm.nih.gov/pmc/articles/PMC3005487/?report= commentator (Accessed 22 September 2014).Brown, N. (2012) Cardiovascular opinions of Anti-Diabetic Agents Focus on source Pressure Effects of Incretin-Based Therapies, Journal of American Society of Hypertension, 6(3), pp. 163 168. Online. Available at http//www.ncbi.nlm.nih.gov/pmc/articles/PMC3422131/ (Accessed 22 September 2014).Burge, T. (2012) The Effects of GLP-1 on Cardiovascular Health. Available at http//www.diabetesincontrol.com/articles/54-feature/13201-the-effects-of-glp-1-on-cardiovascular-health (Accessed 11 September 2014).Hausenloy, D. J. and Yellon, D. M. (2008) GLP-1 Therapy Beyond Glucose Control, Circulation Heartfailure, 1, pp. 147 149. Online. Available at http//circheartfailure.ahajournals.org/ matter/1/3/147.full (Accessed 11 September 2014).NICE (2014) Managing type 2 diabetes. Available at http//pathways.nice.org.uk/pathways/diabetespath=view%3A/pathways/diabetes/managing-type-2-diabetes.xml heart=view-index (Accessed 17 September 2014).Sheikh, A. (2013 ) aspire cardiovascular effects of glucagon like peptide-1, Diabetology Metabolic Syndrome, pp. 5 47. Online. Available at http//www.dmsjournal.com/content/5/1/47 (Accessed 11 September 2014).Wang, B., Zhong, J., Lin, H., Zhao, Z., Yan, Z., He, H., Ni, Y., Liu, D. and Zhu, Z. (2013) argumentation pressure-lowering effects of GLP-1 receptor agonists exenatide and liraglutide a meta-analysis of clinical trials, Diabetes, Obesity Metabolism, 15(8), pp. 737 749. Online. Available at http//www.ncbi.nlm.nih.gov/pubmed/23433305 (Accessed 23 September 2014).World Heart Federation (2014) Cardiovascular disease risk factors. Available at http//www.world-heart-federation.org/cardiovascular-health/cardiovascular-disease-risk-factors/ (Accessed 17 September 2014).Yusuf, S., Hawken, S., Ounpuu, S., Dans T, Avezum, A., Lanas, F., McQueen, M., Budaj, A., Pais, P., Varigos, J., Lisheng, L. and INTERHEART Study Investigators (2004) Effect of potentially modifiable risk factors associated with m yocardial infarction in 52 countries (the INTERHEART study) case-control study, Lancet, 364(9438), pp. 937-52. Online. Available at http//www.ncbi.nlm.nih.gov/pubmed/15364185 (Accessed 17 September 2014).Zhao, T. (2013) Glucagon-like peptide-1 (GLP-1) and protective effects in cardiovascular disease a new therapeutic admittance for myocardial protection, Cardiovascular Diabetology, pp. 12 90. Online. Available at http//www.cardiab.com/content/12/1/90 (Accessed 11 September 2014).