TY - JOUR
T1 - Efficacy and safety of tirzepatide, GLP-1 receptor agonists, and other weight loss drugs in overweight and obesity
T2 - a network meta-analysis
AU - Pan, Xin Hui
AU - Tan, Bryan
AU - Chin, Yip Han
AU - Lee, Ethan Cheng Zhe
AU - Kong, Gwyneth
AU - Chong, Bryan
AU - Kueh, Martin
AU - Khoo, Chin Meng
AU - Mehta, Anurag
AU - Majety, Priyanka
AU - Grandhi, Gowtham R.
AU - Dimitriadis, Georgios K.
AU - Foo, Roger
AU - Chew, Nicholas W.S.
AU - Le Roux, Carel W.
AU - Mamas, Mamas A.
AU - Chan, Mark Y.
N1 - Funding Information:
Carel W. Le Roux: Receives grants from Anabio and serves on advisory boards of Novo Nordisk, Herbalife, GI Dynamics, Eli Lilly, Johnson & Johnson, Glia, Keyron, and Boehringer Ingelheim outside the area of work commented on here. Mark Y. Chan: Receives speaker's fees and research grants from Astra Zeneca, Abbott Technologies, and Boston Scientific. The other authors declared no conflict of interest.
Publisher Copyright:
© 2024 The Obesity Society.
PY - 2024/5
Y1 - 2024/5
N2 - Objective: This network meta-analysis evaluates the efficacy and safety of tirzepatide compared to glucagon-like peptide-1 receptor agonists (GLP-1 RA) and other weight loss drugs in the treatment of overweight and obesity. Methods: MEDLINE, Embase, and Cochrane CENTRAL were searched for randomized controlled trials on tirzepatide, GLP-1 RA, and weight loss drugs approved by the US Food and Drug Administration. A network meta-analysis was performed, drawing direct and indirect comparisons between treatment groups. Network diagrams and surface under the cumulative ranking curve analysis were performed for primary (≥5%, ≥10%, ≥15%, absolute weight loss) and secondary outcomes and adverse effects. Results: Thirty-one randomized controlled trials, involving more than 35,000 patients, were included in this study. Tirzepatide 15 mg ranked in the top three across weight-related parameters, glycemic profile (glycated hemoglobin), lipid parameters (total cholesterol, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, triglycerides), and blood pressure. Tirzepatide 15 mg had the highest efficacy compared with placebo for achieving ≥15% weight loss (risk ratio 10.24, 95% CI: 6.42–16.34). As compared to placebo, tirzepatide and GLP-1 RA across all doses had significant increases in gastrointestinal adverse effects. Conclusions: The superiority of tirzepatide and GLP-1 RA in inducing weight loss and their ability to target multiple metabolic parameters render them promising candidates in the treatment of patients with overweight and obesity.
AB - Objective: This network meta-analysis evaluates the efficacy and safety of tirzepatide compared to glucagon-like peptide-1 receptor agonists (GLP-1 RA) and other weight loss drugs in the treatment of overweight and obesity. Methods: MEDLINE, Embase, and Cochrane CENTRAL were searched for randomized controlled trials on tirzepatide, GLP-1 RA, and weight loss drugs approved by the US Food and Drug Administration. A network meta-analysis was performed, drawing direct and indirect comparisons between treatment groups. Network diagrams and surface under the cumulative ranking curve analysis were performed for primary (≥5%, ≥10%, ≥15%, absolute weight loss) and secondary outcomes and adverse effects. Results: Thirty-one randomized controlled trials, involving more than 35,000 patients, were included in this study. Tirzepatide 15 mg ranked in the top three across weight-related parameters, glycemic profile (glycated hemoglobin), lipid parameters (total cholesterol, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, triglycerides), and blood pressure. Tirzepatide 15 mg had the highest efficacy compared with placebo for achieving ≥15% weight loss (risk ratio 10.24, 95% CI: 6.42–16.34). As compared to placebo, tirzepatide and GLP-1 RA across all doses had significant increases in gastrointestinal adverse effects. Conclusions: The superiority of tirzepatide and GLP-1 RA in inducing weight loss and their ability to target multiple metabolic parameters render them promising candidates in the treatment of patients with overweight and obesity.
UR - http://www.scopus.com/inward/record.url?scp=85186540425&partnerID=8YFLogxK
U2 - 10.1002/oby.24002
DO - 10.1002/oby.24002
M3 - Review article
C2 - 38413012
AN - SCOPUS:85186540425
SN - 1930-7381
VL - 32
SP - 840
EP - 856
JO - Obesity
JF - Obesity
IS - 5
ER -