Biologic and small molecule therapies for psoriasis in individuals with Down syndrome: Two cases and a systematic review
- PMID: 40717838
- PMCID: PMC12290259
- DOI: 10.1177/2050313X251359029
Biologic and small molecule therapies for psoriasis in individuals with Down syndrome: Two cases and a systematic review
Abstract
Down syndrome (DS), also known as trisomy 21, is a genetic condition linked to a higher prevalence of skin disorders, including psoriasis, which affects up to 8% of individuals. DS patients with psoriasis present unique management considerations, including a theoretical increased risk of infectious complications with immunosuppressive therapies. This report includes two cases and a systematic review summarizing available evidence on psoriasis characteristics and treatment outcomes in individuals with DS. We report two DS patients with psoriasis demonstrating variable therapeutic responses: one controlled with acitretin and another requiring secukinumab after multiple treatment failures. To contextualize these findings, we conducted a systematic review following PRISMA guidelines, identifying 10 studies comprising 37 DS patients with psoriasis. Methotrexate was the most frequently failed therapy. Biologics targeting IL-17 and IL-23 pathways achieved the highest rates of complete resolution. These findings reflect Th1/Th17-driven inflammation in DS and highlight the need for individualized, pathway-specific management strategies.
Keywords: biologics; down syndrome; psoriasis; small molecules; trisomy 21.
© The Author(s) 2025.
Conflict of interest statement
The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: Dr. Ronald Vender - Grants/Research Support/Speakers Bureau/Honoraria: AbbVie, Alumis, Amgen, Arcutis, Bausch Health/Valeant, Boehringer Ingelheim, Bristol Myers Squibb, Celltrion, Dermavant, Dermira, DiCE Pharmaceuticals, DiCE Therapeutics, Eli Lilly and Company, Galderma, Incyte, Jamp, Janssen, Leo, Meiji Seika Pharma, Nimbus Therapeutics, Novartis, Pfizer, Sanofi-Aventis/Genzyme, Sandoz, Sun Pharma, Takeda, UCB Pharma, Zai Lab Co. Ltd. The remaining authors Ms. Moshkovich and Mr. Perlmutter have no relevant disclosures.
References
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