» Articles » PMID: 25115635

Effect of GLP-1 Receptor Agonists on Waist Circumference Among Type 2 Diabetes Patients: a Systematic Review and Network Meta-analysis

Overview
Journal Endocrine
Specialty Endocrinology
Date 2014 Aug 14
PMID 25115635
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Glucagon-like peptide-1 receptor agonists (GLP-1RAs) are increasingly used in patients with type 2 diabetes. However, the effect on abdominal obesity has not yet been confirmed. The study aimed to systematically evaluate the effect of GLP-1RAs on waist circumference in patients with type 2 diabetes. MEDLINE, EMBASE, the Cochrane library and www.clinicaltrialgov were searched through October 31, 2013. Randomized controlled trials with available data were selected if they compared GLP-1 RAs with placebo and traditional anti-diabetic drugs with a duration≥8 weeks. Weighted mean difference was estimated using random-effect model. Network meta-analysis was performed to supplement direct comparisons. Seventeen trials with 12 treatments were included. Overall, significant reductions on waist circumference following treatment of liraglutide--1.8 mg once daily (-5.24 cm, 95% CI -7.68, -2.93), liraglutide--1.2 mg once daily (-4.73 cm, 95% CI -6.68, -2.65) and exenatide--10 μg twice daily (-1.34 cm, 95 % CI -2.00, -0.75) were detected versus placebo. The reduction effect was more evident when compared with insulin and thiazolidinediones (range -1.71 to -8.03 cm). Compared with exenatide, liraglutide--0.6 mg once daily, taspoglutide, liraglutide--1.2 mg once daily and liraglutide--1.8 mg once daily significantly decreased waist circumference from -3.32 to -6.01 cm. Besides, liraglutide--1.8 mg once daily significantly decreased waist circumference by -1.73 cm (95 % CI -3.04, -0.55) versus sitagliptin, whereas no significant difference following liraglutide--1.2-mg-once-daily treatment was detected compared with liraglutide--1.8 mg once daily and sitagliptin. Reduction was observed with statistical significance for exenatide--10 μg twice daily compared with exenatide--5 μg twice daily (-1.21 cm, 95% CI -2.43, -0.06). Ranking probability analysis indicated liraglutide--1.8 mg once daily and liraglutide--1.2 mg once daily decreased waist circumference most among all 12 treatments with probability of 98.36% and 91.82%, respectively. Some GLP-1RAs, especially liraglutide--1.8 mg once daily and liraglutide--1.2 mg once daily, were associated with a significant reduction in waist circumference.

Citing Articles

Glucagon-Like Peptide-1 (GLP-1) Receptor Agonists: Exploring Their Impact on Diabetes, Obesity, and Cardiovascular Health Through a Comprehensive Literature Review.

Hamed K, Alosaimi M, Ali B, Alghamdi A, Alkhashi T, Alkhaldi S Cureus. 2024; 16(9):e68390.

PMID: 39355484 PMC: 11444311. DOI: 10.7759/cureus.68390.


Comparative Efficacy and Safety of Glucagon-like Peptide-1 Receptor Agonists in Children and Adolescents with Obesity or Overweight: A Systematic Review and Network Meta-Analysis.

Liu L, Shi H, Shi Y, Wang A, Guo N, Tao H Pharmaceuticals (Basel). 2024; 17(7).

PMID: 39065679 PMC: 11279917. DOI: 10.3390/ph17070828.


Efficacy and Safety of a Biosimilar Liraglutide (Melitide) Versus the Reference Liraglutide (Victoza) in People with Type 2 Diabetes Mellitus: A Randomized, Double-Blind, Noninferiority Clinical Trial.

Esteghamati A, Zamanzadeh M, Malek M, Khaledi M, Monavari A, Najafi L Diabetes Ther. 2023; 14(11):1889-1902.

PMID: 37707701 PMC: 10570258. DOI: 10.1007/s13300-023-01462-w.


Sex Differences in Response to Treatment with Glucagon-like Peptide 1 Receptor Agonists: Opportunities for a Tailored Approach to Diabetes and Obesity Care.

Rentzeperi E, Pegiou S, Koufakis T, Grammatiki M, Kotsa K J Pers Med. 2022; 12(3).

PMID: 35330453 PMC: 8950819. DOI: 10.3390/jpm12030454.


Mechanisms of Cardiorenal Protection of Glucagon-Like Peptide-1 Receptor Agonists.

Tommerdahl K, Nadeau K, Bjornstad P Adv Chronic Kidney Dis. 2021; 28(4):337-346.

PMID: 34922690 PMC: 9119551. DOI: 10.1053/j.ackd.2021.06.001.


References
1.
Bhushan R, Elkind-Hirsch K, Bhushan M, Butler W, Duncan K, Marrioneaux O . Improved glycemic control and reduction of cardiometabolic risk factors in subjects with type 2 diabetes and metabolic syndrome treated with exenatide in a clinical practice setting. Diabetes Technol Ther. 2009; 11(6):353-9. DOI: 10.1089/dia.2008.0090. View

2.
Brunton S . GLP-1 receptor agonists vs. DPP-4 inhibitors for type 2 diabetes: is one approach more successful or preferable than the other?. Int J Clin Pract. 2014; 68(5):557-67. PMC: 4238422. DOI: 10.1111/ijcp.12361. View

3.
Kadowaki T, Namba M, Imaoka T, Yamamura A, Goto W, Boardman M . Improved glycemic control and reduced bodyweight with exenatide: A double-blind, randomized, phase 3 study in Japanese patients with suboptimally controlled type 2 diabetes over 24 weeks. J Diabetes Investig. 2014; 2(3):210-7. PMC: 4014921. DOI: 10.1111/j.2040-1124.2010.00084.x. View

4.
van Bloemendaal L, Ten Kulve J, la Fleur S, IJzerman R, Diamant M . Effects of glucagon-like peptide 1 on appetite and body weight: focus on the CNS. J Endocrinol. 2013; 221(1):T1-16. DOI: 10.1530/JOE-13-0414. View

5.
Bunck M, Diamant M, Eliasson B, Corner A, Shaginian R, Heine R . Exenatide affects circulating cardiovascular risk biomarkers independently of changes in body composition. Diabetes Care. 2010; 33(8):1734-7. PMC: 2909051. DOI: 10.2337/dc09-2361. View