Recommendations for cardiovascular risk assessment and treatment in spondyloarthritis and psoriatic disease

Diego Araiza-Garaygordobil1, Carla A Berrio-Becerra1, Emmanuel Tapia2

  • 1Coronary Care Unit and Department of Cardiovascular Emergency, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.

Insights

Psoriatic disease and spondyloarthritis increase cardiovascular risk due to inflammation, often underestimated by standard tools. Early identification and anti-inflammatory treatments are key for better patient outcomes.

Area of Science:

  • Rheumatology
  • Cardiology
  • Immunology

Background:

  • Psoriatic disease (PD) and spondyloarthritis (SpA) are linked to higher risks of atherosclerotic cardiovascular disease (ASCVD).
  • Chronic inflammation, endothelial dysfunction, and metabolic changes drive this increased cardiovascular risk.
  • Traditional cardiovascular risk assessment tools often underestimate the actual risk in patients with PD and SpA.

Purpose of the Study:

  • To review and synthesize evidence on the association between PD, SpA, and cardiovascular disease (CVD).
  • To evaluate strategies for enhancing the clinical identification and management of CVD risk in these patient populations.

Main Methods:

  • A narrative review methodology was employed.
  • Included were observational studies, clinical trials, prior reviews, and expert opinions from a multidisciplinary panel.

Main Results:

  • Patients with PD and SpA exhibit an elevated incidence of acute myocardial infarction and cerebrovascular disease.
  • Persistent inflammation and metabolic disturbances significantly contribute to the underestimated cardiovascular risk.
  • Current risk assessment tools are insufficient for accurately evaluating CVD risk in this cohort.

Conclusions:

  • More precise and personalized cardiovascular risk assessment is necessary for patients with PD and SpA.
  • Implementing targeted anti-inflammatory therapies and early risk identification strategies can improve clinical outcomes.
  • These interventions have the potential to reduce cardiovascular morbidity and mortality in individuals with PD and SpA.

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