Key result
Semaglutide reduces MACE by ~20% in non-diabetic obesity alongside substantial weight loss.
Why the study?
The clinical efficacy of novel GLP-1 receptor agonists in obesity therapy and prevention of cardiovascular and renal complications requires systematic review and synthesis.
Do GLP-1 receptor agonists improve weight loss and reduce cardiovascular and renal complications in patients with obesity?
Systematic Review
Do GLP-1 receptor agonists improve weight loss and reduce cardiovascular and renal complications in patients with obesity?
GLP-1 receptor agonists offer multidirectional benefits beyond glycemic control, combining profound weight reduction with significant cardiovascular and renal protection in patients with metabolic disease.
GLP-1 receptor agonists merit priority for obese patients without diabetes to achieve weight loss plus MACE reduction; confirms and extends SELECT trial results in systematic synthesis.
Objective: The aim of this article is to systematically review and synthesize current knowledge on the use of glucagon-like peptide-1 receptor agonists (GLP-1RAs) in obesity therapy and their role in the prevention of cardiovascular and renal complications [1, 2]. The paper focuses on evaluating the clinical efficacy of novel molecules, such as semaglutide and tirzepatide, and analyzing molecular mechanisms extending beyond glycemic control [3, 4]. Methodology: An analysis of the literature from 2017–2026 was conducted, including 30 selected publications, comprising the results of key phase III trials (STEP, SURMOUNT, SELECT programs), meta-analyses, and real-world evidence studies [5, 6]. The analysis evaluated data on BMI reduction, the risk of major adverse cardiovascular events (MACE), and parameters of renal and cardiac function [7, 8]. Results: The analysis demonstrated that modern GLP-1RAs allow for a body mass reduction of 14.9–20.9%, which in certain populations constitutes an alternative to bariatric surgery [9, 10, 11]. It was shown that the use of semaglutide reduces the risk of MACE by 20% in patients with obesity without diabetes (SELECT trial) [12] and improves prognosis in patients with heart failure with preserved ejection fraction (HFpEF) [13]. Additionally, significant nephroprotective and anti-inflammatory effects were confirmed, manifested by a reduction in hsCRP levels and stabilization of atherosclerotic plaques [14, 15, 16]. Conclusions: GLP-1 receptor agonists constitute the foundation of a new therapeutic strategy, combining effective obesity treatment with multiorgan protection [17]. Despite proven efficacy, challenges such as high therapy costs, the risk of losing fat-free mass, and implementation Barries require further optimization of patient care [18, 19, 20]
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Strugała et al. (2026) conducted a systematic review in Obesity and cardiovascular complications. GLP-1 receptor agonists vs. Placebo or bariatric surgery (depending on included study) was evaluated on Body mass reduction and incidence of major adverse cardiovascular events (MACE). Modern GLP-1 receptor agonists enable body mass reductions of 15-20% and, as demonstrated with semaglutide, reduce the risk of major adverse cardiovascular events by 20% in obese patients without diabetes.
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