Patients with psoriasis are at increased risk for other comorbid diseases that involve inflammatory processes. There have been studies that link psoriasis and Crohn’s disease (CD) and ulcerative colitis (UC), two forms of inflammatory bowel disease (IBD). As progress has been made to understand the pathogenesis of both diseases, treatment options have expanded, including using biologics that targeting TNF-a and IL-12/23 to treat both psoriasis and IBD. Using biologics that inhibiting the IL-17 pathway are effective to treat psoriasis and psoriatic arthritis (PsA), but it is not known whether this particular treatment negatively affects existing IBD or may even induce first-time CD or UC because of conflicting data on incidence rates (IRs) of CD and UC among psoriasis patients in clinical trials.
Therefore, a recent nationwide study sought to examine the incidence and risk of CD and UC in patients with psoriasis treated with topical, systemic nonbiologic, and biologic therapy. The study consisted of 235,038 patients with psoriasis and 235,038 matched non-psoriasis individuals from the general population, all without a history of CD or UC at baseline. Patients were followed for twenty years. The results showed that there was a significantly increased risk of CD and UC among patients with psoriasis. However, less than 1% developed UC or CD over the 20 year time period. The longer patients had psoriasis, the higher their risk of CD (but not UC). There was no difference in where the IBD was located anatomically between patients with psoriasis and those in the matched population. Patients receiving biologic therapy for psoriasis did not have an increased IBD risk compared with the general population.
The authors state that this is likely because many anti-psoriatic biologics are also effective in treating symptoms of IBD, thereby postponing time to diagnosis. The authors conclude that based on this long-term study, there is an increased risk of CD and UC in patients with psoriasis and that female sex and PsA were noticeable risk factors for IBD.