Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Sep:98:104-111.
doi: 10.1016/j.metabol.2019.06.012. Epub 2019 Jun 27.

Initial injectable therapy in type 2 diabetes: Key considerations when choosing between glucagon-like peptide 1 receptor agonists and insulin

Affiliations
Review

Initial injectable therapy in type 2 diabetes: Key considerations when choosing between glucagon-like peptide 1 receptor agonists and insulin

Anastasia-Stefania Alexopoulos et al. Metabolism. 2019 Sep.

Abstract

Managing type 2 diabetes is complex and necessitates careful consideration of patient factors such as engagement in self-care, comorbidities and costs. Since type 2 diabetes is a progressive disease, many patients will require injectable agents, usually insulin. Recent ADA-EASD guidelines recommend glucagon-like peptide 1 receptor agonists (GLP-1 RAs) as first injectable therapy in most cases. The basis for this recommendation is the similar glycemic efficacy of GLP-1 RAs and insulin, but with GLP-1 RAs promoting weight loss instead of weight gain, at lower hypoglycemia risk, and with cardiovascular benefits in patients with pre-existing cardiovascular disease. GLP-1 RAs also reduce burden of glucose self-monitoring. However, tolerability and costs are important considerations, and notably, rates of drug discontinuation are often higher for GLP-1 RAs than basal insulin. To minimize risk of gastrointestinal symptoms patients should be started on lowest doses of GLP-1 RAs and up-titrated slowly. Overall healthcare costs may be lower with GLP-1 RAs compared to insulin. Though patient-level costs may still be prohibitive, GLP-1 RAs can replace 50-80 units of insulin daily and reduce costs associated with glucose self-monitoring. Decisions regarding initiating injectable therapy should be individualized. This review provides a framework to guide decision-making in the real-world setting.

PubMed Disclaimer

References

    1. Ringborg A, Lindgren P, Yin DD, Martinell M, and Stalhammar J, “Time to insulin treatment and factors associated with insulin prescription in Swedish patients with type 2 diabetes,” Diabetes Metab, vol. 36, pp. 198–203, June 2010. - PubMed
    1. Machado-Alba JE, Machado-Duque ME, and Moreno-Gutierrez PA, “Time to and factors associated with insulin initiation in patients with type 2 diabetes mellitus,” Diabetes Res Clin Pract, vol. 107, pp. 332–7, March 2015. - PubMed
    1. Davies MJ, D’Alessio DA, Fradkin J, Kernan WN, Mathieu C, Mingrone G, et al., “Management of Hyperglycemia in Type 2 Diabetes, 2018. A Consensus Report by the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD),” Diabetes Care, vol. 41, pp. 2669–2701, December 2018. - PMC - PubMed
    1. Guerci B, Charbonnel B, Gourdy P, Hadjadj S, Hanaire H, Marre M, et al., “Efficacy and adherence of glucagon-like peptide-1 receptor agonist treatment in patients with type 2 diabetes mellitus in real-life settings,” Diabetes Metab, Jan 21 2019. - PubMed
    1. Li Z, Zhang Y, Quan X, Yang Z, Zeng X, Ji L, et al., “Efficacy and Acceptability of Glycemic Control of Glucagon-Like Peptide-1 Receptor Agonists among Type 2 Diabetes: A Systematic Review and Network Meta-Analysis,” PLoS One, vol. 11, p. e0154206, 2016. - PMC - PubMed

Publication types

MeSH terms