Improvement in glycated haemoglobin evaluated by baseline body mass index: a meta-analysis of the liraglutide phase III clinical trial programme.
Diabetes Obes Metab · 2016
Last updated 2026-05-28A review of seven clinical trials involving 3,222 people with type 2 diabetes found that the effectiveness of liraglutide (at doses of 1.2 mg or 1.8 mg) in lowering blood sugar control did not depend on a person's starting body weight. For the 1.8 mg dose, a very small and likely insignificant trend was observed, where a 10 kg/m² higher starting BMI was linked to a 0.10%-point greater reduction in blood sugar control.
AI summary of the abstract below.
| Journal | Diabetes Obes Metab, 2016 |
|---|---|
| Citations | 10 |
| Relative citation ratio | 0.32 |
| NIH percentile | 20 |
| Molecules | liraglutide |
| Conditions studied | Type 2 Diabetes, Obesity |
Abstract
In the liraglutide clinical trial programme, liraglutide 1.2 and 1.8 mg were found to effectively lower glycated haemoglobin (HbA1c) in patients with type 2 diabetes (T2D). It is unknown whether baseline body mass index (BMI) is a predictor of change in HbA1c observed during a clinical trial with liraglutide or placebo treatment. The present meta-analysis of patient-level data, using pooled data from seven phase III trials [LEAD-1-6 and the liraglutide versus sitagliptin trial (LIRA-DPP-4)] for liraglutide 1.2, 1.8 mg and placebo (n = 3222), identified no significant correlation between baseline BMI (<20 kg/m(2) up to 45 kg/m(2) ) and HbA1c reduction for placebo or liraglutide 1.2 mg, and a modest, clinically non-relevant, association for liraglutide 1.8 mg [-0.010 (95% confidence interval -0.020, -0.001)], whereby a 10 kg/m(2) increase in baseline BMI corresponded to 0.10%-point (1.1 mmol/mol) greater HbA1c reduction. In summary, reductions in HbA1c obtained during clinical trials with liraglutide or placebo treatment were independent of baseline BMI.
Verbatim abstract via PubMed 26662611 ↗
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