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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.
Abstract:
Patients with inflammatory arthritis have increased risk of cardiovascular diseases (CVDs) compared with the general population. Subclinical carotid atherosclerosis and increased arterial stiffness are also common in these patients, which may serve as surrogate end points for cardiovascular (CV) events in clinical trials. Although exact mechanisms are still unclear, persistent systemic inflammation in patients with inflammatory arthritis may contribute to the development of CVD. Dysregulated innate immunity pathways in these patients may also play a role in accelerating atherosclerosis. During the last decade, effective suppression of inflammation by biological disease-modifying antirheumatic drugs has improved the disease outcome dramatically in patients with inflammatory arthritis. Growing evidence suggests that antitumor necrosis factor (TNF) therapy may prevent CVD in patients with rheumatoid arthritis. Nonetheless, data on non-TNF biologics are limited. Whether anti-TNF therapy may prevent CVD in patients with spondyloarthritis also remained unclear. In this review, we summarized the effect of both anti-TNF and non-TNF biologics on the CV system, including traditional CVD risk factors, endothelial function, arterial stiffness, subclinical atherosclerosis, and clinical CVD in patients with inflammatory arthritis.
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