Liraglutide, a Once-daily Human GLP-1 Analogue, Added to a Sulphonylurea over 26 Weeks Produces Greater Improvements in Glycaemic and Weight Control Compared with Adding Rosiglitazone or Placebo in Subjects with Type 2 Diabetes (LEAD-1 SU)
Overview
Authors
Affiliations
Aim: To compare the effects of combining liraglutide (0.6, 1.2 or 1.8 mg/day) or rosiglitazone 4 mg/day (all n >or= 228) or placebo (n = 114) with glimepiride (2-4 mg/day) on glycaemic control, body weight and safety in Type 2 diabetes.
Methods: In total, 1041 adults (mean +/- sd), age 56 +/- 10 years, weight 82 +/- 17 kg and glycated haemoglobin (HbA(1c)) 8.4 +/- 1.0% at 116 sites in 21 countries were stratified based on previous oral glucose-lowering mono : combination therapies (30 : 70%) to participate in a five-arm, 26-week, double-dummy, randomized study.
Results: Liraglutide (1.2 or 1.8 mg) produced greater reductions in HbA(1c) from baseline, (-1.1%, baseline 8.5%) compared with placebo (+0.2%, P < 0.0001, baseline 8.4%) or rosiglitazone (-0.4%, P < 0.0001, baseline 8.4%) when added to glimepiride. Liraglutide 0.6 mg was less effective (-0.6%, baseline 8.4%). Fasting plasma glucose decreased by week 2, with a 1.6 mmol/l decrease from baseline at week 26 with liraglutide 1.2 mg (baseline 9.8 mmol/l) or 1.8 mg (baseline 9.7 mmol/l) compared with a 0.9 mmol/l increase (placebo, P < 0.0001, baseline 9.5 mmol/l) or 1.0 mmol/l decrease (rosiglitazone, P < 0.006, baseline 9.9 mmol/l). Decreases in postprandial plasma glucose from baseline were greater with liraglutide 1.2 or 1.8 mg [-2.5 to -2.7 mmol/l (baseline 12.9 mmol/l for both)] compared with placebo (-0.4 mmol/l, P < 0.0001, baseline 12.7 mmol/l) or rosiglitazone (-1.8 mmol/l, P < 0.05, baseline 13.0 mmol/l). Changes in body weight with liraglutide 1.8 mg (-0.2 kg, baseline 83.0 kg), 1.2 mg (+0.3 kg, baseline 80.0 kg) or placebo (-0.1 kg, baseline 81.9 kg) were less than with rosiglitazone (+2.1 kg, P < 0.0001, baseline 80.6 kg). Main adverse events for all treatments were minor hypoglycaemia (< 10%), nausea (< 11%), vomiting (< 5%) and diarrhoea (< 8%).
Conclusions: Liraglutide added to glimepiride was well tolerated and provided improved glycaemic control and favourable weight profile.
Teng Y, Fan X, Yu R, Yang X BMC Endocr Disord. 2024; 24(1):278.
PMID: 39719583 PMC: 11668020. DOI: 10.1186/s12902-024-01805-z.
Obesity Medications and Their Impact on Cardiovascular Health: A Narrative Review.
Islam K, Islam R, Tong V, Shami M, Allen K, Brodtmann J Cureus. 2024; 16(10):e71875.
PMID: 39559664 PMC: 11573306. DOI: 10.7759/cureus.71875.
Mahapatro A, Bozorgi A, Obulareddy S, Jain S, Korsapati R, Kumar A Ann Med Surg (Lond). 2024; 86(11):6602-6618.
PMID: 39525800 PMC: 11543192. DOI: 10.1097/MS9.0000000000002592.
Liraglutide innovations: a comprehensive review of patents (2014-2024).
Pandey A, Goyal A Pharm Pat Anal. 2024; 13(1-3):73-89.
PMID: 39316579 PMC: 11449036. DOI: 10.1080/20468954.2024.2366693.
Mechanisms of action and therapeutic applications of GLP-1 and dual GIP/GLP-1 receptor agonists.
Liu Q Front Endocrinol (Lausanne). 2024; 15:1431292.
PMID: 39114288 PMC: 11304055. DOI: 10.3389/fendo.2024.1431292.