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Comparative effectiveness of liraglutide in the treatment of type 2 diabetes

Authors Rigato M, Fadini GP

Received 20 January 2014

Accepted for publication 7 February 2014

Published 18 March 2014 Volume 2014:7 Pages 107—120

DOI https://doi.org/10.2147/DMSO.S37644

Checked for plagiarism Yes

Review by Single-blind

Peer reviewer comments 3


Mauro Rigato, Gian Paolo Fadini

Department of Medicine, University Hospital of Padova, Padova, Italy

Abstract: Type 2 diabetes is characterized by a progressive decline in beta cell function, with consequent worsening of glycemic control. The ideal antihyperglycemic treatment should achieve good and sustained glycemic control, with a low risk of hypoglycemia and no weight gain. This paper reviews the efficacy and tolerability of liraglutide, a glucagon-like peptide-1 receptor agonist approved for the treatment of type 2 diabetes. Once-daily injection of liraglutide (at doses of 1.2 mg and 1.8 mg), as monotherapy or in combination with one or two oral antihyperglycemic agents, was associated with greater improvements in glycemic control compared with active comparators or placebo in several controlled, randomized Phase III trials, including the six trials of the LEAD (Liraglutide Effect and Action in Diabetes) program. Liraglutide also improved beta cell function, body weight, systolic blood pressure, and lipid profile, thereby achieving many of the goals of ideal antihyperglycemic therapy. Liraglutide was generally well tolerated in the Phase III trials. The most common adverse events were nausea, vomiting, and diarrhea, usually of mild to moderate intensity. The observed rate of pancreatitis was low and comparable with that of the general diabetic population. In conclusion, although most trials were relatively short and focused on surrogate endpoints, liraglutide emerges as an effective and well tolerated treatment for type 2 diabetes, carrying a low risk of hypoglycemia, weight loss, and possible reduction of cardiovascular risk.

Keywords: body weight, hypoglycemia, cardiovascular, incretin

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