Efficacy and safety of tirzepatide, GLP‐1 receptor agonists, and other weight loss drugs in overweight and obesity: a network meta‐analysis

Author:

Pan Xin‐Hui1,Tan Bryan1ORCID,Chin Yip Han2ORCID,Lee Ethan Cheng Zhe3,Kong Gwyneth2,Chong Bryan1,Kueh Martin4ORCID,Khoo Chin Meng15,Mehta Anurag6,Majety Priyanka7,Grandhi Gowtham R.6,Dimitriadis Georgios K.89ORCID,Foo Roger110,Chew Nicholas W. S.110ORCID,Le Roux Carel W.11ORCID,Mamas Mamas A.1213,Chan Mark Y.110

Affiliation:

1. Yong Loo Lin School of Medicine National University of Singapore Singapore

2. Ministry of Health Holdings Ministry of Health Singapore

3. Lee Kong Chian School of Medicine Nanyang Technological University Singapore

4. Royal College of Surgeons in Ireland & University College Dublin Malaysia Campus George Town Malaysia

5. Department of Endocrinology National University Hospital Singapore

6. VCU Health Pauley Heart Center, Division of Cardiology, Department of Internal Medicine Virginia Commonwealth University Richmond Virginia USA

7. Department of Endocrinology, Diabetes and Metabolism Virginia Commonwealth University Health Richmond Virginia USA

8. Faculty of Life Sciences and Medicine School of Life Course Sciences, King's College London London UK

9. Department of Endocrinology King's College Hospital NHS Foundation Trust, Denmark Hill London UK

10. Department of Cardiology National University Heart Centre Singapore

11. Diabetes Complications Research Centre University College Dublin Dublin Ireland

12. Keele Cardiovascular Research Group, Centre for Prognosis Research Keele University Keele UK

13. Department of Cardiology Royal Stoke University Hospital Stoke‐on‐Trent UK

Abstract

AbstractObjectiveThis 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.MethodsMEDLINE, 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.ResultsThirty‐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.ConclusionsThe 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.

Publisher

Wiley

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