[Translated article] Glucagon-Like Peptide-1 Agonists for Treating Obesity in Patients With Immune-Mediated Skin Diseases.
Actas Dermosifiliogr · 2024
Last updated 2026-05-28GLP-1 agonists, a newer class of obesity drugs, have led to greater weight loss in clinical trials and real-world settings than orlistat, which was previously the only approved obesity drug in the EU. These drugs work by affecting satiety receptors. While research on GLP-1 agonists in people with obesity and inflammatory skin diseases like psoriasis or hidradenitis suppurativa is limited, early results suggest they may be helpful for managing weight in these patients.
AI summary of the abstract below.
| Journal | Actas Dermosifiliogr, 2024 |
|---|---|
| Citations | 6 |
| Relative citation ratio | 2.68 |
| NIH percentile | 81 |
| Molecules | — |
| Conditions studied | Obesity |
Abstract
Psoriasis and hidradenitis suppurativa are often associated with obesity. Because chronic low-grade inflammation underlies these 2 diseases, they can progress to more severe forms in patients with obesity if weight-reduction measures are not taken. This review covers pharmacologic alternatives for treating obesity, with emphasis on the benefits associated with the novel use of glucagon-like peptide-1 (GLP-1) agonists that act on satiety receptors. These drugs have led to greater weight loss in clinical trials and real-world settings than orlistat, which until recently was the only drug approved for treating obesity in the European Union. Although experience with GLP-1 agonists in patients with obesity and inflammatory skin diseases is currently scarce, the promising results reported suggest they may offer a useful tool for managing obesity.
Verbatim abstract via PubMed 37918631 ↗