AI Article Synopsis

  • Paradoxical psoriasis (PP) can develop in patients with inflammatory bowel diseases (IBD) and psoriasis when treated with anti-TNF-α drugs, highlighting a unique response to treatment.
  • A study of 161 patients found that 39 experienced PP, revealing clinical patterns like a higher occurrence in females and a link with the drug adalimumab among IBD patients.
  • Genetic analysis showed specific SNPs associated with PP susceptibility, indicating that genetic factors might influence how patients respond to anti-TNF-α therapy, which could be important for clinical decisions.

Article Abstract

Paradoxical psoriasis (PP) may occur during treatment with anti-tumor necrosis factor-alpha (TNF-α) drugs in various chronic immune-mediated diseases, mainly inflammatory bowel diseases (IBD) and psoriasis. In this study, clinical and genetic characteristics of PP arising in IBD and psoriatic patients were investigated to identify disease-specific markers of the paradoxical effect. A total of 161 IBD and psoriatic patients treated with anti-TNF-α drugs were included in the study. Of these patients, 39 developed PP. All patients were characterized for the main clinical-pathologic characteristics and genotyped for six candidate single nucleotide polymorphisms (SNPs) selected for their possible role in PP susceptibility. In IBD patients, the onset of PP was associated with female sex, presence of comorbidities, and use of adalimumab. IBD patients with PP had a higher frequency of the rs1799964 rare allele ( = 0.006) compared with cases without the paradoxical effect, and a lower frequency of the human leucocyte antigen ()- rs10484554 rare allele ( = 0.03) compared with psoriatic patients with PP. Overall, these findings point to specific clinical and genetic characteristics of IBD patients with PP and provide data showing that genetic variability may be related to the paradoxical effect of anti-TNF-α drugs with possible implications into clinical practice.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7660646PMC
http://dx.doi.org/10.3390/ijms21217873DOI Listing

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