Key result
Glucagon-like peptide-1 receptor agonists significantly reduced visceral adipose tissue (SMD -0.54) and subcutaneous adipose tissue compared to control groups in patients with type 2 diabetes.
Why the study?
GLP-1 receptor agonists reduce glucose and promote weight loss in type 2 diabetes, but few studies have reported their effect on fat distribution.
Do GLP-1 receptor agonists reduce visceral and subcutaneous adipose tissue in patients with type 2 diabetes?
Meta-Analysis (n=541)
Do GLP-1 receptor agonists reduce visceral and subcutaneous adipose tissue in patients with type 2 diabetes?
Standardized Mean Difference: -0.54 (95% CI -0.92–-0.17)
p-value: p=0.005
GLP-1 receptor agonists significantly reduce both visceral and subcutaneous adipose tissue in patients with type 2 diabetes, with a numerically greater effect on visceral fat.
Aims/Introduction Glucagon‐like peptide‐1 receptor agonists (GLP‐1Ras) are widely used to treat type 2 diabetes. They not only reduce glucose, but also have a positive effect on weight loss. However, few studies have reported the effect of GLP‐1Ras on fat distribution. Materials and Methods PubMed, Cochrane, Embase and ClinicalTrials.gov were searched for randomized controlled trials on GLP‐1Ras and type 2 diabetes, published from inception to June 2021. Our main outcomes were the reductions of visceral adipose tissue (VAT) and subcutaneous adipose tissue (SAT). Other anthropometric outcomes were also assessed. We used the Cochrane Collaboration tools to assess the risk of bias in the included studies. The quality of the evidence was assessed using the Grades of Recommendation, Assessment, Development and Evaluation profiler version 3.6. Review Manager 5.4.1 and Stata 16.0 were used for data analysis. Results A total of 10 studies involving 541 patients were included. Compared with the control groups, the GLP‐1Ras groups showed reductions in VAT (standard mean difference −0.54, 95% confidence interval [CI] −0.92, −0.17, I 2 = 79%, P = 0.005) and SAT (standard mean difference −0.44, 95% CI −0.60, −0.27, I 2 = 44%, P < 0.00001). In addition, bodyweight (weighted mean difference −3.59, 95% CI −4.30, −2.88, I 2 = 0%, P < 0.00001), waist circumference (weighted mean difference −3.09, 95% CI −4.66, −1.52, I 2 = 70%, P = 0.0001) and body mass index (weighted mean difference −1.11, 95% CI −1.35, −0.86, I 2 = 47%, P < 0.00001) were significantly decreased. According to the Grades of Recommendation, Assessment, Development and Evaluation approach, the level of evidence was low or moderate. Conclusion This study highlights that GLP‐1Ras, especially liraglutide and exenatide, might play an active role in fat distribution in patients with type 2 diabetes. After treatment with GLP‐1Ras, both VAT and SAT decreased, and the decrease of VAT was numerically greater than that of SAT.
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Duan et al. (2022) conducted a meta-analysis in Type 2 diabetes (n=541). Glucagon-like peptide-1 receptor agonists (GLP-1Ras) vs. Placebo or active comparator drugs was evaluated on Reduction of visceral adipose tissue (VAT) (SMD -0.54, 95% CI -0.92, -0.17, p=0.005). Glucagon-like peptide-1 receptor agonists significantly reduced visceral adipose tissue (SMD -0.54) and subcutaneous adipose tissue compared to control groups in patients with type 2 diabetes.
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