Crosstalk between Inflammation and Atherosclerosis in Rheumatoid Arthritis and Systemic Lupus Erythematosus: Is There

Marta Chiara Sircana1, Gian Luca Erre1, Floriana Castagna1

  • 1Department of Medical, Surgical and Pharmacology, University of Sassari, 07100 Sassari, Italy.

PubMed

Insights

Inflammation drives atherosclerosis in rheumatoid arthritis and systemic lupus erythematosus, explaining early cardiovascular disease beyond traditional risk factors. Chronic inflammation

Area of Science:

  • Immunology
  • Cardiovascular Medicine
  • Rheumatology

Background:

  • Cardiovascular disease (CVD) is a major cause of death in rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE).
  • Traditional CVD risk factors do not fully account for the high incidence of early-onset CVD in these autoimmune diseases.
  • Atherosclerosis pathogenesis is increasingly understood as an inflammation-centric process.

Purpose of the Study:

  • To review the pathogenesis of atherosclerosis in RA and SLE.
  • To highlight RA and SLE as models for chronic inflammation's impact on cardiovascular health.
  • To explore immune system involvement in atherosclerosis within these diseases.

Main Methods:

  • Review of current literature on atherosclerosis in RA and SLE.
  • Examination of the roles of inflammasomes, immune cells (neutrophils, macrophages, lymphocytes), and inflammatory mediators.
  • Investigation of autoantigens (e.g., oxidized LDL) and autoantibodies (e.g., anti-beta2-glycoprotein I) in disease progression.

Main Results:

  • Chronic inflammation, mediated by immune cells and cytokines, is central to atherosclerosis in RA and SLE.
  • Specific immune pathways and autoantibodies contribute significantly to cardiovascular risk.
  • The inflammatory milieu in RA and SLE accelerates atherosclerotic plaque development.

Conclusions:

  • Atherosclerosis in RA and SLE is driven by chronic systemic inflammation.
  • Targeting inflammatory pathways offers potential therapeutic strategies for cardiovascular risk reduction in these patients.
  • Understanding immune-mediated mechanisms is crucial for managing CVD in autoimmune diseases.

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