Glucagon-like peptide 1 receptor agonists as a potential way to overcome treatment resistance in psoriasis and psoriatic arthritis

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Authors: Aleksander M. Lila, Tatiana V Korotaeva, Тарас Сергеевич Паневин, Evgeniy G. Zotkin
Cited by: 1
References: 54

Abstract

Patients with psoriasis (PsO) and psoriatic arthritis (PsA) are characterized by a high prevalence of concomitant obesity and metabolic disorders, and an increased body mass index (BMI) increases the likelihood of PsA development in patients with PsO. Obesity, as well as PsO/PsA, is associated with increased cardiovascular risk and reduced quality of life. Achieving minimal disease activity in PsO/PsA in obese patients may be challenging. Effective and sustained BMI reduction (regardless of the method) increases the likelihood of achieving remission and enhances the efficacy of tumor necrosis factor α (TNFα) inhibitors.This review presents the results of studies on the effects of the most commonly used drug class for obesity treatment — glucagon-like peptide 1 receptor agonists — on PsO/PsA activity, as well as their combined use with biologic agents.

Fields of Study & Subjects

Diabetes Treatment and Management Psoriasis: Treatment and Pathogenesis Adenosine and Purinergic Signaling

Publication details

Journal / source
Modern Rheumatology Journal
Publisher
IMA Press, LLC
Volume
20
Issue
3
Pages
84–90
Publication date
24 June 2026
Language
RU