You are here

  • Home
  • Online First
  • Subcutaneous liraglutide reduces weight and improves metabolic control in obese participants

Article Text

Article menu

other Versions

Download PDFPDF
Therapeutics/Prevention
Randomised controlled trial
Subcutaneous liraglutide reduces weight and improves metabolic control in obese participants
  1. Kyaw Soe,
  2. Kathleen M Dungan
  1. The Ohio State University, Columbus, Ohio, USA
  1. Correspondence to : Dr Kathleen M Dungan, The Ohio State University, 5th floor, McCampbell Hall, 1581 Dodd Dr, Columbus, OH 43210, USA; kathleen.dungan{at}osumc.edu

https://doi.org/10.1136/ebmed-2015-110273

Statistics from Altmetric.com

    Request Permissions

    If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

    Commentary on: Pi-Sunyer X, Astrup A, Fujioka K, et al., SCALE Obesity and Prediabetes NN8022-1839 Study Group. A randomized, controlled trial of 3.0 mg of liraglutide in weight management. N Engl J Med 2015;373:11–22.OpenUrlCrossRefPubMed

    Context

    Obesity is a major health problem of the 21st century and has been one of the primary contributors to the rising prevalence of type 2 diabetes mellitus (T2DM). A 5–10% loss of total body weight can reduce risk of T2DM onset.1 However, it is challenging to achieve and maintain weight loss that is sufficient for sustained metabolic benefits. Liraglutide is a glucagon-like peptide-1 (GLP-1) receptor agonist that was initially developed for treatment of hyperglycaemia in patients with T2DM. It was also noted to have non-glycaemic benefits such as weight loss2 and …

    View Full Text

    Footnotes

    • Contributors KMD and KS contributed equally to writing and revising this manuscript.

    • Competing interests KMD serves as site primary investigator for multicenter trials sponsored by Sanofi, GSK, Grifols, Merck, Astra Zeneca and Regeneron and as primary investigator for investigator initiated trial funded by Merck. KMD is involved in advising activities for Eli Lilly and consulting activities for GSK. KS serves as site primary investigator for multicenter trials sponsored by Eli Lilly.

    • Provenance and peer review Commissioned; internally peer reviewed.