Targeting inflammation in the prevention of cardiovascular disease in patients with inflammatory arthritis

Jiayun Shen1, Qing Shang1, Lai-Shan Tam1

  • 1Department of Medicine and Therapeutics, The Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.

Insights

Patients with inflammatory arthritis face higher cardiovascular disease (CVD) risks. This review examines how biologic therapies, including anti-TNF and non-TNF drugs, impact cardiovascular health in these patients.

Area of Science:

  • Rheumatology
  • Cardiology
  • Immunology

Background:

  • Patients with inflammatory arthritis exhibit elevated cardiovascular disease (CVD) risks compared to the general population.
  • Subclinical atherosclerosis and arterial stiffness are prevalent in inflammatory arthritis, potentially serving as surrogate endpoints for cardiovascular events.
  • Persistent systemic inflammation and dysregulated innate immunity in inflammatory arthritis are implicated in accelerating atherosclerosis and CVD development.

Purpose of the Study:

  • To review the effects of biologic disease-modifying antirheumatic drugs (bDMARDs) on the cardiovascular system in patients with inflammatory arthritis.
  • To evaluate the impact of anti-tumor necrosis factor (TNF) therapies and non-TNF biologics on traditional CVD risk factors, endothelial function, arterial stiffness, subclinical atherosclerosis, and clinical CVD.
  • To clarify the role of anti-TNF therapy in preventing CVD in rheumatoid arthritis and spondyloarthritis.

Main Methods:

  • Systematic review of existing literature on biologic therapies and cardiovascular outcomes in inflammatory arthritis.
  • Analysis of studies investigating the effects of anti-TNF and non-TNF biologics on various cardiovascular parameters.
  • Synthesis of data regarding clinical cardiovascular events in patients treated with different classes of biologics.

Main Results:

  • Biologic therapies, particularly anti-TNF agents, have shown promise in improving cardiovascular outcomes in rheumatoid arthritis.
  • Data on the cardiovascular effects of non-TNF biologics are still limited, necessitating further research.
  • The precise impact of anti-TNF therapy on CVD prevention in spondyloarthritis requires additional investigation.

Conclusions:

  • Effective inflammation suppression with biologics has improved disease outcomes in inflammatory arthritis.
  • Anti-TNF therapy may offer cardiovascular benefits in certain inflammatory arthritis populations, but more research is needed for non-TNF biologics and spondyloarthritis.
  • Further studies are crucial to fully elucidate the cardiovascular protective potential of various biologic therapies in inflammatory arthritis.

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