AI Article Synopsis

  • Systemic inflammation is key to understanding psoriasis and was evaluated through various inflammatory markers in patients with psoriasis vulgaris and psoriatic arthritis.
  • The study found that certain markers, like neutrophil and CRP levels, were linked to the severity of psoriasis and the likelihood of developing psoriatic arthritis.
  • Higher levels of inflammatory markers before treatment were associated with lower rates of continuing conventional therapies but did not impact retention rates for biologic treatments.

Article Abstract

Systemic inflammation plays a central role in the pathophysiology of psoriasis. This study examined accessible systemic inflammatory markers in patients with psoriasis vulgaris and psoriatic arthritis. We aimed to evaluate their association with psoriasis severity, the presence of arthritis, and drug continuation rates. The findings revealed that neutrophil, monocyte, and platelet count, neutrophil/lymphocyte ratio, monocyte/lymphocyte ratio, inflammation response index, immune/inflammation index (SII), and CRP were positively correlated with Area and Severity Index scores. Patients presenting with higher platelet/lymphocyte ratio (PLR) or CRP values were more likely to be diagnosed with psoriatic arthritis than with psoriasis vulgaris in the multivariate regression analysis. Importantly, patients with higher pretreatment neutrophil or platelet count, PLR, and SII were associated with lower treatment continuation rates of conventional systemic agents. Higher pretreatment scores of systemic inflammatory markers did not affect treatment retention rates of biologics. These findings suggest that several accessible systemic inflammatory markers may effectively assess underlying systemic inflammation and may provide an indication for a therapeutic approach in patients with psoriasis vulgaris and psoriatic arthritis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10145777PMC
http://dx.doi.org/10.3390/jcm12083046DOI Listing

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