Comparative risk of psoriatic arthritis in psoriasis patients on immunomodulators

<b>Background:</b> Psoriatic arthritis (PsA) is a rapidly progressive arthritis that is difficult to prevent and treat. The comparative risk of PsA development in psoriasis patients prescribed PsA-approved immunomodulators is unknown. <b>Methods:</b> We assessed the 3-year risk of PsA in psoriasis patients on immunomodulators of IL-12, 17, 23, tumor necrosis factor alpha, JAK1, and JAK3. Using the TriNetX Research Network, we identified patients with psoriasis and the use of an immunomodulatory agent. The immunomodulatory agents assessed included adalimumab, infliximab, ixekizumab, secukinumab, tildrakizumab, certolizumab pegol, risankizumab, etanercept, guselkumab, and ustekinumab. <b>Results:</b> Overall, IL-23 inhibitors risankizumab, guselkumab, and ustekinumab had the greatest decreased risk of PsA. <b>Conclusion:</b> Physicians can consider risankizumab, guselkumab, and ustekinumab as treatment options for psoriasis patients with PsA risk factors to mitigate disease progression and improve patients' quality of life.

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Publication Details

Journal
Baylor University Medical Center Proceedings
Published
2025-12-08
DOI
https://doi.org/10.1080/08998280.2025.2596529
Primary Topic
Psoriasis: Treatment and Pathogenesis
Type
article
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article

Comparative risk of psoriatic arthritis in psoriasis patients on immunomodulators

George Golovko, Ayezel Munoz Gonzalez, Travis S. Dowdle, M. Schmidt
Baylor University Medical Center Proceedings
Psoriasis: Treatment and Pathogenesis
article

Comparative risk of psoriatic arthritis in psoriasis patients on immunomodulators

George Golovko, Ayezel Munoz Gonzalez, Travis S. Dowdle, M. Schmidt
article en

Abstract

<b>Background:</b> Psoriatic arthritis (PsA) is a rapidly progressive arthritis that is difficult to prevent and treat. The comparative risk of PsA development in psoriasis patients prescribed PsA-approved immunomodulators is unknown. <b>Methods:</b> We assessed the 3-year risk of PsA in psoriasis patients on immunomodulators of IL-12, 17, 23, tumor necrosis factor alpha, JAK1, and JAK3. Using the TriNetX Research Network, we identified patients with psoriasis and the use of an immunomodulatory agent. The immunomodulatory agents assessed included adalimumab, infliximab, ixekizumab, secukinumab, tildrakizumab, certolizumab pegol, risankizumab, etanercept, guselkumab, and ustekinumab. <b>Results:</b> Overall, IL-23 inhibitors risankizumab, guselkumab, and ustekinumab had the greatest decreased risk of PsA. <b>Conclusion:</b> Physicians can consider risankizumab, guselkumab, and ustekinumab as treatment options for psoriasis patients with PsA risk factors to mitigate disease progression and improve patients' quality of life.

Baylor University Medical Center ProceedingsVol. 39(2)
The University of Texas Medical Branch at Galveston (US)
Openalex Percentile: Top 55%
Psoriasis: Treatment and Pathogenesis
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