Literature DB >> 21389295

Optimizing outcomes for GLP-1 agonists.

Jeffrey S Freeman1.   

Abstract

The management of type 2 diabetes mellitus and, in particular, blood glucose levels can be complex and challenging for physicians and patients. Many patients are frustrated with the agents currently available because they have associated limitations of weight gain, hypoglycemia, and tolerability issues. Advantages of glucagon-like peptide-1 (GLP-1) agonists include their efficacy in lowering blood glucose levels, their lack of association with weight gain, and their indirect association with weight loss. Patients likely to benefit from GLP-1 agonist therapy are those in the early stages of the disease and those in need of sufficient benefit from an agent with good efficacy. Setting appropriate expectations for patients is important, as well as explaining the significance of glucose control and reminding patients that this is the main goal of therapy. Patients (and physicians) who have concerns about hypoglycemia can be reassured that GLP-1 agonists work only in the presence of hyperglycemia. Longer-acting GLP-1 agonists are dosed less frequently, appear to be associated with less nausea, and may be associated with better rates of adherence than shorter-acting agents. When initiating therapy with GLP-1 agonists, doses should be gradually escalated to minimize gastrointestinal adverse effects. The dose of a sulfonylurea may need to be lowered if a GLP-1 agonist is added. A review of possible adverse effects, contraindications, dosing and administration techniques, and expected benefits of therapy is provided in the present article to optimize success rates with this new class of agents.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21389295

Source DB:  PubMed          Journal:  J Am Osteopath Assoc        ISSN: 0098-6151


  7 in total

1.  Optimizing the Care of Patients With Type 2 Diabetes Using Incretin-Based Therapy: Focus on GLP-1 Receptor Agonists.

Authors:  Mansur Shomali
Journal:  Clin Diabetes       Date:  2014-01

2.  High-fat diet changes the temporal profile of GLP-1 receptor-mediated hypophagia in rats.

Authors:  Joram D Mul; Denovan P Begg; Jason G Barrera; Bailing Li; Emily K Matter; David A D'Alessio; Stephen C Woods; Randy J Seeley; Darleen A Sandoval
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2013-04-24       Impact factor: 3.619

3.  Comparison of safety and tolerability with continuous (exenatide once weekly) or intermittent (exenatide twice daily) GLP-1 receptor agonism in patients with type 2 diabetes.

Authors:  T Ridge; T Moretto; L MacConell; R Pencek; J Han; C Schulteis; L Porter
Journal:  Diabetes Obes Metab       Date:  2012-07-19       Impact factor: 6.577

4.  Additive feeding inhibitory and aversive effects of naltrexone and exendin-4 combinations.

Authors:  N-C Liang; N T Bello; T H Moran
Journal:  Int J Obes (Lond)       Date:  2012-02-07       Impact factor: 5.095

5.  Therapeutic Options for the Management of Postprandial Glucose in Patients With Type 2 Diabetes on Basal Insulin.

Authors:  Debbie A Hinnen
Journal:  Clin Diabetes       Date:  2015-10

6.  Initiating Titratable Fixed-Ratio Combinations of Basal Insulin Analogs and Glucagon-Like Peptide-1 Receptor Agonists: What You Need to Know.

Authors:  Neil Skolnik; Debbie Hinnen; Yan Kiriakov; Melissa L Magwire; John R White
Journal:  Clin Diabetes       Date:  2018-04

7.  iGlarLixi: A New Once-Daily Fixed-Ratio Combination of Basal Insulin Glargine and Lixisenatide for the Management of Type 2 Diabetes.

Authors:  Debbie Hinnen; Jodi Strong
Journal:  Diabetes Spectr       Date:  2018-05
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.