GLPwatch

Anti-obesity therapy for cardiovascular disease prevention: potential expected roles of glucagon-like peptide-1 receptor agonists.

Cardiovasc Diabetol · 2022

Last updated 2026-05-28

Obesity increases the risk of heart disease, but lifestyle changes alone often don’t lower this risk enough. Older weight-loss drugs can help people lose weight but haven’t clearly shown they reduce heart disease risk. Newer drugs called GLP-1 receptor agonists, however, have shown promise in both weight loss and preventing obesity-related heart disease.

AI summary of the abstract below.

JournalCardiovasc Diabetol, 2022
Citations10
Relative citation ratio0.68
NIH percentile38
Molecules
Conditions studied Obesity, Cardiovascular Risk Reduction

Abstract

Obesity is characterized by visceral fat accumulation and various metabolic disturbances that cause metabolic syndrome and obesity-related cardiovascular diseases (ORCVDs). Hence, treatments targeting obesity should also prevent ORCVDs. Nonetheless, lifestyle modification therapy alone is still insufficient to reduce the risk of ORCVDs, although most cardiovascular guidelines still list it as the only treatment for obesity. Additionally, conventional anti-obesity drugs, such as orlistat, phentermine-topiramate, and naltrexone-bupropion, can reduce body weight but have not demonstrated a clear reduction in the risk of ORCVDs. To overcome this unmet clinical need, newer anti-obesity drugs must exhibit not only sufficient and long-lasting weight loss but also obvious cardiovascular benefits. Given recent clinical findings and evidences, in this context glucagon-like peptide-1 receptor agonist is currently available as a candidate that is clinically positioned as a first-line anti-obesity agent for the effective prevention of ORCVDs in people with obesity.

Verbatim abstract via PubMed 36068534 ↗