TY - JOUR
T1 - Laparoscopic adjustable gastric banding with liraglutide in adults with obesity and type 2 diabetes (GLIDE)
T2 - a pilot randomised placebo controlled trial
AU - Coelho, Claudia
AU - Dobbie, Laurence J.
AU - Crane, James
AU - Douiri, Abdel
AU - Learoyd, Annastazia E.
AU - Okolo, Olanike
AU - Panagiotopoulos, Spyros
AU - Pournaras, Dimitri J.
AU - Ramar, Sasindran
AU - Rubino, Francesco
AU - Singhal, Rishi
AU - le Roux, Carel W.
AU - Taheri, Shahrad
AU - McGowan, Barbara
N1 - Funding Information:
We thank the participants for taking part in the GLIDE trial. We would also like to thank the clinical research teams at each study site who worked on the GLIDE trial. This study was funded by Novo Nordisk Investigator Led Grant. Novo-Nordisk had no input in the design, conduct, or interpretation of the results.
Funding Information:
AEL does not declare any conflicts of interest. CLR declares grants to his institution from the Irish Research Council, Health Research Board, Science Foundation Ireland and Anabio; consulting fees from NovoNordisk, Eli Lily, Johnson & Johnson, Boehringer Ingelheim, GI dynamics and Herbalife; Honoraria for presentations and support for attending meetings from NovoNordisk, Herbalife and Johnson & Johnson; unpaid leadership roles for the Irish Society for Nutrition and Metabolism and stocks in Keyron. BM is a shareholder in Reset Health and also performs Advisory and educational work for Novonordisk and Advisory work for Lilly. DP declares honoraria and consulting fees from Johnson & Johnson, honoraria from Medtronic and NovoNordisk and unpaid leadership roles at the Royal College of Surgeons, England. All other authors do not declare any conflicts of interest.
Publisher Copyright:
© 2023, The Author(s).
PY - 2023/11
Y1 - 2023/11
N2 - Introduction: Obesity drives type 2 diabetes (T2DM) development. Laparoscopic adjustable gastric banding (LAGB) has lower weight reduction than other bariatric procedures. Liraglutide, a GLP-1 receptor agonist, improves weight and glycaemic control in patients with T2DM. This study aimed to determine the efficacy and safety of liraglutide 1.8 mg in participants undergoing LAGB. Methods: GLIDE, a pilot randomised, double-blind, placebo-controlled trial, evaluated LAGB with either liraglutide 1.8 mg or placebo in participants with T2DM and obesity. Participants were randomised (1:1) to 6-months therapy post-LAGB, with further 6 months off-treatment follow-up. The primary outcome was change in HbA1c from randomisation to the end of treatment, secondary outcomes included body weight change. A sample size of 58 (29 per group) had 80% power to detect a 0.6% difference in HbA1c between groups. Results: Twenty-seven participants were randomised to liraglutide (n = 13) or placebo (n = 14). Multivariate analysis showed no difference between placebo and liraglutide arms in HbA1c at 6 months (HbA1c:0.2 mmol/mol, −11.3, 11.6, p = 0.98) however, at 12 months HbA1c was significantly higher in the liraglutide arm (HbA1c:10.9 mmol/mol, 1.1, 20.6, p = 0.032). There was no difference between arms in weight at 6 months (BW:2.0 kg, −4.2, 8.1, p = 0.50), however, at 12 months weight was significantly higher in the liraglutide arm (BW:8.2 kg, 1.6, 14.9, p = 0.02). There were no significant differences in adverse events between groups. Conclusions: Our pilot data suggest no additional improvement in glycaemic control or BW with LAGB and liraglutide therapy. However, this trial was significantly underpowered to detect a significant change in the primary or secondary outcomes. Further trials are needed to investigate whether GLP-1 agonists, and particularly with more effective weekly agents (i.e. semaglutide or tirzepatide), are of benefit following metabolic surgery. Clinical trial registration: EudraCT number 2015-005402-11. [Figure not available: see fulltext.]
AB - Introduction: Obesity drives type 2 diabetes (T2DM) development. Laparoscopic adjustable gastric banding (LAGB) has lower weight reduction than other bariatric procedures. Liraglutide, a GLP-1 receptor agonist, improves weight and glycaemic control in patients with T2DM. This study aimed to determine the efficacy and safety of liraglutide 1.8 mg in participants undergoing LAGB. Methods: GLIDE, a pilot randomised, double-blind, placebo-controlled trial, evaluated LAGB with either liraglutide 1.8 mg or placebo in participants with T2DM and obesity. Participants were randomised (1:1) to 6-months therapy post-LAGB, with further 6 months off-treatment follow-up. The primary outcome was change in HbA1c from randomisation to the end of treatment, secondary outcomes included body weight change. A sample size of 58 (29 per group) had 80% power to detect a 0.6% difference in HbA1c between groups. Results: Twenty-seven participants were randomised to liraglutide (n = 13) or placebo (n = 14). Multivariate analysis showed no difference between placebo and liraglutide arms in HbA1c at 6 months (HbA1c:0.2 mmol/mol, −11.3, 11.6, p = 0.98) however, at 12 months HbA1c was significantly higher in the liraglutide arm (HbA1c:10.9 mmol/mol, 1.1, 20.6, p = 0.032). There was no difference between arms in weight at 6 months (BW:2.0 kg, −4.2, 8.1, p = 0.50), however, at 12 months weight was significantly higher in the liraglutide arm (BW:8.2 kg, 1.6, 14.9, p = 0.02). There were no significant differences in adverse events between groups. Conclusions: Our pilot data suggest no additional improvement in glycaemic control or BW with LAGB and liraglutide therapy. However, this trial was significantly underpowered to detect a significant change in the primary or secondary outcomes. Further trials are needed to investigate whether GLP-1 agonists, and particularly with more effective weekly agents (i.e. semaglutide or tirzepatide), are of benefit following metabolic surgery. Clinical trial registration: EudraCT number 2015-005402-11. [Figure not available: see fulltext.]
UR - http://www.scopus.com/inward/record.url?scp=85170364873&partnerID=8YFLogxK
U2 - 10.1038/s41366-023-01368-4
DO - 10.1038/s41366-023-01368-4
M3 - Article
AN - SCOPUS:85170364873
SN - 0307-0565
VL - 47
SP - 1132
EP - 1142
JO - International Journal of Obesity
JF - International Journal of Obesity
IS - 11
ER -