Read Full Article HereAt the Fall Clinical PA/NP 2025 Meeting, Dr. Ben Lockshin, MD, a board-certified dermatologist based in Rockville, Maryland, discussed the emerging role of glucagon-like peptide-1 (GLP-1) receptor agonists in dermatologic care, particularly in patients with psoriasis and obesity.
GLP-1 receptor agonists, including semaglutide and tirzepatide, are well-established for their efficacy in weight reduction. However, recent clinical interest is exploring their role in improving skin conditions, particularly when used alone or in combination with biologics in patients with moderate to severe psoriasis.
“There was actually a study that focused on using semaglutide as a monotherapy to improve skin in patients with PASI [psoriasis area and severity index] scores of 10 or greater,” said Lockshin. “We saw that there was not only weight reduction, but also skin improvement, as well as improvement in DLQI [dermatology life quality index] in those patients.”
While the majority of available data focuses on weight loss as the primary end point, ongoing trials are examining the added value of GLP-1 agents in dermatology. Notably, Eli Lilly is sponsoring 2 studies investigating combination therapy using tirzepatide (a dual glucose-dependent insulinotropic polypeptide [GIP]/GLP-1 receptor agonist [RA]) and ixekizumab (an IL-17A antagonist) in patients with elevated body mass index (BMI) and moderate to severe psoriasis.
These combination trials aim to determine whether reducing BMI can enhance the efficacy of biologics in psoriasis treatment. “We also have a blinded study looking at the combination of tirzepatide and ixekizumab versus ixekizumab alone,” Lockshin noted. “This could be a game changer for patients who haven’t responded optimally to biologics due to elevated BMI.”
