Effect of survodutide, a glucagon and GLP-1 receptor dual agonist, on weight loss: a meta-analysis of randomized controlled trials

被引:0
|
作者
Wan, Haijun [1 ]
Xu, Nuo [1 ]
Wang, Lijuan [1 ]
Liu, Yaping [2 ]
Fatahi, Somaye [3 ]
Sohouli, Mohammad Hassan [4 ]
Guimaraes, Nathalia Sernizon [5 ]
机构
[1] Nanjing Univ, Jinling Hosp, Affiliated Hosp, Dept Gastroenterol & Hepatol,Med Sch, Nanjing, Peoples R China
[2] Nanjing Univ, Nanjing Jinling Hosp, Affiliated Hosp, Day Operat Management Ctr,Med Sch, Nanjing, Peoples R China
[3] Shahid Beheshti Univ Med Sci, Fac Nutr & Food Technol, Dept Clin Nutr & Dietet, Tehran, Iran
[4] Univ Tehran Med Sci, Pediat Gastroenterol & Hepatol Res Ctr, Childrens Med Ctr, Pediat Ctr Excellence, Tehran, Iran
[5] Univ Fed Minas Gerais, Sch Nursing, Dept Nutr, Belo Horizonte, MG, Brazil
来源
DIABETOLOGY & METABOLIC SYNDROME | 2024年 / 16卷 / 01期
关键词
Survodutide; Dual GLP-1/glucagon agonist; Obesity; Weight loss; Meta-analysis; LOSS INTERVENTIONS; OBESITY; OUTCOMES;
D O I
10.1186/s13098-024-01501-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundConsidering the increasing prevalence of obesity/overweight, its treatment or prevention with new interventions can greatly help health and reduce its adverse effects in people. One of these new interventions is investigating the effect of Survodutide as a dual agonist of glucagon and GLP-1 receptors, which seems to be able to influence weight loss processes in different ways. In this study, we investigated the effect of injectable Survodutide on weight loss.MethodsIn order to identify all randomized controlled trials that investigated the effects of Survodutide on factores related to obesity, a systematic search was conducted in the original databases using predefined keywords until August 2024. The pooled weighted mean difference and 95% confidence intervals were computed using the random-effects model.ResultsThe Findings from 18 treatment arms with 1029 participants indicated significant reductions in weight (WMD: -8.33 kg; 95% CI: -10.80, -5.86; I2 = 99.6%), body mass index (BMI) (WMD:-4.03 kg/m2; 95% CI: -4.86, -3.20; I2 = 72.7%), and waist circumferences (WC) (WMD: -6.33 cm; 95% CI: -8.85 to -3.81; I2 = 99.5%) following the Survodutide injection compared to the control group. Subgroup analysis reveals that longer interventions (more than 16 weeks) and higher doses (more than 2 mg/week) of Survodutide are associated with more significant reductions in weight and WC. These results were also observed in the meta-regression analysis.ConclusionsThe results of this meta-analysis show that Survodutide is effective in reducing weight, BMI and waist circumference, especially with longer interventions and higher doses.
引用
收藏
页数:11
相关论文
共 50 条
  • [1] Efficacy and safety of the dual GIP and GLP-1 receptor agonist tirzepatide for weight loss: a meta-analysis of randomized controlled trials
    Yasmin Luz Lima de Mesquita
    Izabela Pera Calvi
    Isabela Reis Marques
    Sara Almeida Cruz
    Eduardo Messias Hirano Padrao
    Pedro Emanuel de Paula Carvalho
    Caroliny Hellen Azevedo da Silva
    Rhanderson Cardoso
    Filipe Azevedo Moura
    Vladimir Vitalievich Rafalskiy
    International Journal of Obesity, 2023, 47 : 883 - 892
  • [2] Efficacy and safety of the dual GIP and GLP-1 receptor agonist tirzepatide for weight loss: a meta-analysis of randomized controlled trials
    de Mesquita, Yasmin Luz Lima
    Calvi, Izabela Pera
    Marques, Isabela Reis
    Cruz, Sara Almeida
    Padrao, Eduardo Messias Hirano
    Carvalho, Pedro Emanuel de Paula
    da Silva, Caroliny Hellen Azevedo
    Cardoso, Rhanderson
    Moura, Filipe Azevedo
    Rafalskiy, Vladimir Vitalievich
    INTERNATIONAL JOURNAL OF OBESITY, 2023, 47 (10) : 883 - 892
  • [3] Safety and efficacy of GLP-1 and glucagon receptor dual agonist for the treatment of type 2 diabetes and obesity: a systematic review and meta-analysis of randomized controlled trials
    Deng, Bixin
    Ruan, Tiechao
    Lu, Wenting
    Ying, Junjie
    Li, Shiping
    Zhou, Ruixi
    Mu, Dezhi
    ENDOCRINE, 2024, 86 (01) : 15 - 27
  • [4] A Systematic Review and Meta-Analysis of Randomized Controlled Trials in Use of GLP-1 Receptor Agonist in Type 1 Diabetes Mellitus
    Panta, Raju
    Kunwar, Sumit
    Batra, Manav
    Ghimire, Dipesh K. C.
    Mudgal, Mayuri
    Makdissi, Antoine
    Chaudhuri, Ajay
    Dandona, Paresh
    DIABETES, 2017, 66 : A308 - A308
  • [5] Effect of Pemvidutide, a GLP-1/Glucagon Dual Receptor Agonist, on Cardioinflammatory Lipids
    Suschak, John J.
    Georges, Bertrand
    Roberts, M. S.
    Harris, M. Scott
    Browne, Sarah K.
    DIABETES, 2024, 73
  • [6] Use of GLP-1 Receptor Agonists and Occurrence of Thyroid Disorders: a Meta-Analysis of Randomized Controlled Trials
    Hu, Weiting
    Song, Rui
    Cheng, Rui
    Liu, Caihong
    Guo, Rui
    Tang, Wei
    Zhang, Jie
    Zhao, Qian
    Li, Xing
    Liu, Jing
    FRONTIERS IN ENDOCRINOLOGY, 2022, 13
  • [7] Survodutide, a glucagon receptor/GLP-1 receptor (GCGR/GLP-1R) dual agonist, improves cardiometabolic parameters in adults with obesity: analysis of a placebo-controlled, randomised phase 2 trial
    Le Roux, C.
    Steen, O.
    Lucas, K. J.
    Ekinci, E., I
    Startseva, E.
    Unseld, A.
    Hennige, A. M.
    EUROPEAN HEART JOURNAL, 2024, 45
  • [8] GLP-1 receptor agonists and diabetic retinopathy: A meta-analysis of randomized clinical trials
    Kapoor, Ishani
    Sarvepalli, Swara M.
    D'Alessio, David
    Grewal, Dilraj S.
    Hadziahmetovic, Majda
    SURVEY OF OPHTHALMOLOGY, 2023, 68 (06) : 1071 - 1083
  • [9] Effect of pemvidutide, a GLP-1/glucagon dual receptor agonist, on MASLD: A randomized, double-blind, placebo- controlled study
    Harrison, Stephen A.
    Browne, Sarah K.
    Suschak, John J.
    Tomah, Shaheen
    Gutierrez, Julio A.
    Yang, Jay
    Roberts, M. Scot
    Harris, M. Scott
    JOURNAL OF HEPATOLOGY, 2025, 82 (01)
  • [10] Liraglutide, GLP-1 receptor agonist, for chronic weight loss
    Moore, Katherine G.
    Shealy, Kayce
    Clements, Jennifer N.
    EXPERT REVIEW OF ENDOCRINOLOGY & METABOLISM, 2016, 11 (05) : 373 - 378