Glimepiride: evidence-based facts, trends, and observations

Type 2 diabetes mellitus is characterized by insulin resistance and progressive β cell failure; therefore, β cell secretagogues are useful for achieving sufficient glycemic control. Glimepiride is a second-generation sulfonylurea that stimulates pancreatic β cells to release insulin. Additionally, i...

Full description

Bibliographic Details
Main Authors: Basit, Abdul, Riaz, Musarrat, Fawwad, Asher
Format: Online
Language:English
Published: Dove Medical Press 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448454/
id pubmed-3448454
recordtype oai_dc
spelling pubmed-34484542012-10-01 Glimepiride: evidence-based facts, trends, and observations Basit, Abdul Riaz, Musarrat Fawwad, Asher Review Type 2 diabetes mellitus is characterized by insulin resistance and progressive β cell failure; therefore, β cell secretagogues are useful for achieving sufficient glycemic control. Glimepiride is a second-generation sulfonylurea that stimulates pancreatic β cells to release insulin. Additionally, is has been shown to work via several extra pancreatic mechanisms. It is administered as monotherapy in patients with type 2 diabetes mellitus in whom glycemic control is not achieved by dietary and lifestyle modifications. It can also be combined with other antihyperglycemic agents, including metformin and insulin, in patients who are not adequately controlled by sulfonylureas alone. The effective dosage range is 1 to 8 mg/day; however, there is no significant difference between 4 and 8 mg/day, but it should be used with caution in the elderly and in patients with renal or hepatic disease. In clinical studies, glimepiride was generally associated with lower risk of hypoglycemia and less weight gain compared to other sulfonylureas. Glimepiride use may be safer in patients with cardiovascular disease because of its lack of detrimental effects on ischemic preconditioning. It is effective in reducing fasting plasma glucose, post-prandial glucose, and glycosylated hemoglobin levels and is a useful, cost-effective treatment option for managing type 2 diabetes mellitus. Dove Medical Press 2012 2012-08-15 /pmc/articles/PMC3448454/ /pubmed/23028231 http://dx.doi.org/10.2147/HIV.S33194 Text en © 2012 Basit et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Basit, Abdul
Riaz, Musarrat
Fawwad, Asher
spellingShingle Basit, Abdul
Riaz, Musarrat
Fawwad, Asher
Glimepiride: evidence-based facts, trends, and observations
author_facet Basit, Abdul
Riaz, Musarrat
Fawwad, Asher
author_sort Basit, Abdul
title Glimepiride: evidence-based facts, trends, and observations
title_short Glimepiride: evidence-based facts, trends, and observations
title_full Glimepiride: evidence-based facts, trends, and observations
title_fullStr Glimepiride: evidence-based facts, trends, and observations
title_full_unstemmed Glimepiride: evidence-based facts, trends, and observations
title_sort glimepiride: evidence-based facts, trends, and observations
description Type 2 diabetes mellitus is characterized by insulin resistance and progressive β cell failure; therefore, β cell secretagogues are useful for achieving sufficient glycemic control. Glimepiride is a second-generation sulfonylurea that stimulates pancreatic β cells to release insulin. Additionally, is has been shown to work via several extra pancreatic mechanisms. It is administered as monotherapy in patients with type 2 diabetes mellitus in whom glycemic control is not achieved by dietary and lifestyle modifications. It can also be combined with other antihyperglycemic agents, including metformin and insulin, in patients who are not adequately controlled by sulfonylureas alone. The effective dosage range is 1 to 8 mg/day; however, there is no significant difference between 4 and 8 mg/day, but it should be used with caution in the elderly and in patients with renal or hepatic disease. In clinical studies, glimepiride was generally associated with lower risk of hypoglycemia and less weight gain compared to other sulfonylureas. Glimepiride use may be safer in patients with cardiovascular disease because of its lack of detrimental effects on ischemic preconditioning. It is effective in reducing fasting plasma glucose, post-prandial glucose, and glycosylated hemoglobin levels and is a useful, cost-effective treatment option for managing type 2 diabetes mellitus.
publisher Dove Medical Press
publishDate 2012
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448454/
_version_ 1611910903406526464