An update on the safety of insulin-GLP-1 receptor agonist combinations in type 2 diabetes mellitus.
Expert Opin Drug Saf · 2022
Last updated 2026-05-28Three fixed-ratio combinations of insulin and GLP-1 drugs (iGlarLixi and IDegLira) are currently available for type 2 diabetes. Studies show these combinations improve blood sugar control while reducing the risk of low blood sugar compared to insulin alone, and they have a neutral effect on body weight. They also appear to cause fewer stomach-related side effects than GLP-1 drugs used alone.
AI summary of the abstract below.
| Journal | Expert Opin Drug Saf, 2022 |
|---|---|
| Citations | 10 |
| Relative citation ratio | 1.07 |
| NIH percentile | 53 |
| Molecules | — |
| Conditions studied | Type 2 Diabetes |
Abstract
INTRODUCTION: Recent development of novel antidiabetic drugs with proven cardiovascular (CV) and renal benefit and positive effect on body weight enable to take a more complex approach toward the management of type 2 diabetes mellitus (T2DM). Fixed-ratio combinations of insulin-GLP-1 receptor agonist (FRC) utilize complementary mechanisms of action of their individual components and address multiple pathologies linked with T2DM at the same time.
AREAS COVERED: There are currently three FRCs on the market: iGlarLixi (glargine and lixisenatide in 2 different formulations) and IDegLira (degludec and liraglutide). We provide an up-to-date review on the rationale for the use of FRCs and their current position in the management of T2DM. We discuss the available evidence from randomized controlled trials, post hoc analyses, indirect comparative studies and real-world data on their effect on glycemic control, risk of hypoglycemia, body weight, CV safety, and their safety profile.
EXPERT OPINION: FRCs represent an efficacious option for treatment intensification from basal insulin or even the first insulin-based therapy in T2DM. Their excellent glucose-lowering efficacy is complemented with lower risk of hypoglycemia in comparison to basal insulin, neutral effect on body weight and the lower risk of gastrointestinal adverse effects in comparison to GLP-1 receptor agonists.
Verbatim abstract via PubMed 34641742 ↗