Background: Obesity is one of the leading causes of morbidity and mortality
nowadays, with prevalence tripling since the 1970s. Lifestyle modification remains
the cornerstone of treatment, but pharmacotherapy has emerged as a critical
adjunct, including GLP-1R(glucagon-like peptide-1 receptor) agonists. Objective: To
present the efficacy, safety, and clinical implications of GLP-1 receptor agonists in
the treatment of obesity. Methods: A narrative review was based on articles available
in PubMed, NIH, Wiley, The Lancet, and NEJM databases. Keywords included
“obesity”, “GLP-1R agonists”, “semaglutide”, “liraglutide”, “tirzepatide”. Inclusion
criteria encompassed randomized clinical trials, observational studies, metaanalyses,
and review articles published in English between October 2018 and
December 2025. Results: GLP-1 receptor agonists demonstrate significant weight
loss efficacy. Semaglutide achieves weight loss of 11.4–13.9% at 68 weeks, and
liraglutide produces 5.3–5.8% weight loss at 52–56 weeks. Tirzepatide, a dual
GIP/GLP-1 agonist, demonstrates efficacy with even 17.8% weight loss at 72 weeks.
Furthermore, these agents improve cardiometabolic parameters, such as blood
pressure, lipid profiles, and glycemic control. Gastrointestinal adverse events, such
as nausea, vomiting, diarrhea, and constipation, are common but generally mild.
More serious adverse events are rare. Conclusions: GLP-1 receptor agonists are
among the most effective options for the treatment of obesity. They help achieve
clinically significant weight loss and improvements in metabolic parameters. There
is a need for further research to investigate long-term safety and optimal treatment
strategies.
Keywords: obesity, GLP-1R agonists, semaglutide, liraglutide, tirzepatide
