| Literature DB >> 33520865 |
Mandana Hasanzad1,2, Negar Sarhangi2, Shekoufeh Nikfar2,3, Seyed Naser Ostad2,4, Hamid Reza Aghaei Meybodi2,5.
Abstract
Liraglutide is a long-acting human glucagon-like peptide-1 (GLP-1) analogue and an effective treatment for patients with metabolic diseases including type 2 diabetes mellitus (T2DM) and obesity. This review focuses on the mechanism of action of liraglutide as a well-known glucagon-like peptide-1 receptor agonist (GLP-1 RA) in patients with T2DM and obesity. The lower and the higher doses of GLP-1 RAs are used for glycaemic control in T2DM and in obesity respectively. GLP-1 RAs such as liraglutide enhance insulin secretion and inhibit glucagon release via the stimulation of glucagon-like peptide-1 receptors (GLP-1Rs). Liraglutide decreases hemoglobin A1c (HbA1c) in type 2 diabetes (T2D) patients when prescribes as monotherapy or in combination with one or more antidiabetic drugs. Usually, it is well tolerated with minor hypoglycemia in combination therapy. Liraglutide reduces cardiovascular events and related risk factors including improvement of lipid profile and control of blood pressure. Accordingly, it can be cost-effective and may be a budget neutral medication option by considering its protective effect on the cardiovascular system in long-term use in the health care plan. In the near future, by pharmacogenomics approach, prediction of the highest patient's response with the lowest adverse drug reactions and also rationality of drug development will be possible. Liraglutide can be used as a desirable medicine for glycemic control and obesity. It shows extensive evidence based benefits in diabetes complications. In this narrative review, we have summarized and evaluated studies related to the role of liraglutide in clinical practice. © Springer Nature Switzerland AG 2020.Entities:
Keywords: Cardiovascular events; GLP-1 RAs, Liraglutide; Obesity; Pharmacogenomics; Type 2 diabetes
Year: 2020 PMID: 33520865 PMCID: PMC7843728 DOI: 10.1007/s40200-020-00619-9
Source DB: PubMed Journal: J Diabetes Metab Disord ISSN: 2251-6581