Liraglutide Versus SGLT-2 Inhibitors in People with Type 2 Diabetes: A Network Meta-Analysis

Maria Lorenzi1, Uffe Jon Ploug2, Jakob Langer2

  • 1Precision Health Economics, 250-555 12 Street, Oakland, CA, 94607, USA. maria.lorenzi@precisionhealtheconomics.com.

Abstract

Insights

Liraglutide improves glycemic control (HbA1c, FPG) more than SGLT-2 inhibitors in type 2 diabetes. Weight reduction is comparable, with no difference in hypoglycemia risk between these treatments.

Area of Science:

  • Endocrinology
  • Metabolic Diseases
  • Pharmacology

Background:

  • Type 2 diabetes (T2DM) often requires treatment intensification beyond oral antidiabetic drugs (OADs).
  • Liraglutide has demonstrated efficacy in glycemic control and weight reduction.
  • Sodium glucose cotransporter 2 (SGLT-2) inhibitors represent a newer OAD class with proven effectiveness.

Purpose of the Study:

  • To evaluate the relative efficacy of liraglutide versus SGLT-2 inhibitors for T2DM treatment intensification.
  • To compare glycemic control, weight changes, and hypoglycemia risk using network meta-analysis (NMA).

Main Methods:

  • Systematic literature review identifying randomized controlled trials (RCTs) of liraglutide and SGLT-2 inhibitors.
  • Bayesian network meta-analysis (NMA) assessing changes in HbA1c, weight, fasting plasma glucose (FPG), and hypoglycemia risk.
  • Inclusion of trials with placebo or sitagliptin as active comparators to strengthen indirect comparisons.

Main Results:

  • Liraglutide (both doses) showed statistically significant superiority over SGLT-2 inhibitors in improving HbA1c and FPG.
  • SGLT-2 inhibitors, particularly canagliflozin 300 mg, were associated with greater weight reduction.
  • No significant differences in the risk of major or minor hypoglycemia were observed between liraglutide and SGLT-2 inhibitors.

Conclusions:

  • Liraglutide offers superior improvements in HbA1c and FPG compared to SGLT-2 inhibitors for T2DM.
  • Weight reduction is comparable between liraglutide and SGLT-2 inhibitors.
  • This NMA provides valuable comparative insights in the absence of head-to-head trials.

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