Choice of Biologic Immunotherapy for Psoriasis or Psoriatic Arthritis and Its Association With Risk of Major Adverse

Jack Geiger1, Bonit Gill1, Jean Liew2

  • 1J. Geiger, DO, B. Gill, DO, M. Putman, MD, S. Singla, MD, Medical College of Wisconsin, Milwaukee, Wisconsin.

PubMed

Insights

Patients with psoriasis or psoriatic arthritis using biologic disease-modifying antirheumatic drugs (bDMARDs) face similar risks of major adverse cardiac events (MACE) regardless of the drug class. Cardiovascular risk should not influence the choice of bDMARD for these patients.

Area of Science:

  • Rheumatology
  • Cardiology
  • Pharmacology

Background:

  • Psoriasis (PsO) and psoriatic arthritis (PsA) patients have increased risk of major adverse cardiac events (MACE).
  • Biologic disease-modifying antirheumatic drugs (bDMARDs) are used to treat PsO and PsA, but their comparative effect on MACE risk is unclear.

Purpose of the Study:

  • To investigate if the risk of MACE differs among various bDMARD classes in patients with PsO/PsA.
  • To compare the cardiovascular safety profiles of different bDMARDs in this patient population.

Main Methods:

  • Retrospective cohort study using the TriNetX database.
  • Identified new users of tumor necrosis factor inhibitors (TNFi), IL-17A inhibitors (IL-17i), IL-23 inhibitors (IL-23i), or IL-12/23 inhibitors (IL-12/23i).
  • Weighted multinomial Cox proportional hazards regression was used to calculate time-dependent MACE risk, with TNFi as the referent group. Bias was assessed using negative control outcomes.

Main Results:

  • 32,758 new bDMARD users with PsO/PsA were identified.
  • The adjusted risk of MACE was comparable across IL-17i (aHR 0.98), IL-23i (aHR 0.84), and IL-12/23i (aHR 1.08) compared to TNFi.
  • Subset analyses and negative control outcomes supported the primary findings, indicating adequate control of bias.

Conclusions:

  • The risk of MACE does not significantly vary between different classes of bDMARDs in patients with PsO/PsA.
  • Cardiovascular risk should not be a primary factor when selecting a bDMARD for patients with PsO/PsA.
Abstract

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