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SGLT2 inhibitors or GLP-1 receptor agonists as second-line therapy in type 2 diabetes: patient selection and perspectives
Authors Gurgle H, White K, McAdam-Marx C
Received 14 November 2015
Accepted for publication 11 March 2016
Published 4 June 2016 Volume 2016:12 Pages 239—249
DOI https://doi.org/10.2147/VHRM.S83088
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Emre Yalcinkaya
Peer reviewer comments 5
Editor who approved publication: Professor Daniel Duprez
Holly E Gurgle, Karen White, Carrie McAdam-Marx
Department of Pharmacotherapy, University of Utah College of Pharmacy, Salt Lake City, UT, USA
Abstract: Controversy exists regarding the selection of second-line therapy for patients with type 2 diabetes mellitus (T2DM) who are unable to achieve glycemic control with metformin therapy alone. Newer pharmacologic treatments for T2DM include glucagon-like peptide-1 receptor agonists and sodium–glucose cotransporter 2 inhibitors. Both the classes of medication are efficacious, exhibit positive effects on weight, and are associated with minimal risk of hypoglycemia. The purpose of this review is to compare the clinical trial and real-world effectiveness data of glucagon-like peptide-1 receptor agonists versus sodium–glucose cotransporter 2 inhibitors related to A1c reduction, weight loss, cost-effectiveness, cardiovascular outcomes, and safety in patients with T2DM. This review summarizes comparative evidence for providers who are determining which of the two classes may be the most appropriate for a specific patient.
Keywords: type 2 diabetes mellitus, GLP-1 receptor agonist, SGLT2 inhibitor, A1c, weight loss, adverse effect
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