4.3 Review

Incretin-based therapy in type 2 diabetes: An evidence based systematic review and meta-analysis

Journal

JOURNAL OF DIABETES AND ITS COMPLICATIONS
Volume 32, Issue 1, Pages 113-122

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jdiacomp.2016.08.018

Keywords

Clinical aspects of diabetes; Clinical and molecular diabetes; Weight gain; Obesity; Oral antidiabetics

Funding

  1. NIH [K01 DK105108]
  2. Mid-Atlantic Nutrition Obesity Research Center (NORC) under NIH [P30DK072488]
  3. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [K01DK105108, P30DK072488] Funding Source: NIH RePORTER

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Incretin based therapies such as dipeptidyl peptidase-4 inhibitors (DPP-4i) and glucagon-like peptide-1 receptor agonists (GLP-1Ra) are increasingly used for the treatment of Type 2 diabetes mellitus. In clinical practice and in previously performed clinical trials, these agents are often used in combination with other oral anti-diabetic agents (OADs) and Insulin. Prior meta-analytic reviews however do not adequately address the impact of background therapy and active comparator arms. Accordingly, we aimed to further investigate the efficacy of incretin based therapies by updating existing reviews by including clinical trial evidence after 2008; estimating the pooled effect of incretin therapies on glycemic efficacy and weight-loss, stratified by comparator therapy (placebo, mono-therapy, etc.), estimating the impact of background OADs and within class (GLP-1Ra or DPP-4i) comparative efficacy, on glycemia control. 82 randomized controlled trials after 2008 with glycemic control and weight loss as primary end-points were included. Both DPP-4i and GLP-1Ra reduced HbA1c, but only GLP-1Ra caused weight loss when compared to either active comparator drugs or placebo. GLP-1Ra were more effective than DPP-4i in glycemia lowering. Long acting GLP-1Ra were more effective in HbA1c lowering than short acting agents but with similar weight loss effect. The effect of DPP-4i incretin glycemic efficacy was not modified by background therapy used in the study. (C) 2016 Published by Elsevier Inc

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