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Inflammatory arthritis as a novel risk factor for cardiovascular disease
1Department of Rheumatology, Dudley Group of Hospitals NHS Foundation Trust, Russells Hall Hospital, Dudley DY1 2HQ, United Kingdom.
Insights
Cardiovascular disease (CVD) risk is elevated in inflammatory arthritides (IA). Current management requires better risk quantification and targeted interventions for conditions like rheumatoid arthritis (RA), psoriatic arthritis (PsA), and ankylosing spondylitis (AS).
Area of Science:
- Rheumatology
- Cardiology
- Immunology
Background:
- Cardiovascular disease (CVD) is a major comorbidity in inflammatory arthritides (IA), including rheumatoid arthritis (RA), psoriatic arthritis (PsA), and ankylosing spondylitis (AS).
- Increased cardiovascular mortality in IA is linked to accelerated atherosclerosis, driven by both classical risk factors and systemic inflammation.
Purpose of the Study:
- To highlight the significant CVD comorbidity in IA.
- To emphasize the need for improved CVD risk quantification and management strategies in RA, PsA, and AS.
Main Methods:
- Review of existing mortality studies and risk factor analyses in IA.
- Discussion of current gaps in quantifying individual CVD risk.
- Analysis of consensus guidelines for CVD risk management in IA.
Main Results:
- Evidence suggests elevated cardiovascular mortality in RA, PsA, and AS.
- Current methods cannot accurately quantify the combined contribution of classical and novel risk factors to CVD risk in IA.
- There is a need for validated algorithms and large clinical trials to assess interventions.
Conclusions:
- A pragmatic approach to CVD risk management in IA is currently recommended.
- Routine assessment and treatment of CVD risk factors are crucial.
- Further research is needed to develop specific risk prediction tools and evaluate interventions.
Abstract:
Cardiovascular disease (CVD) comorbidity is a significant issue for the inflammatory arthritides (IA). There is a wealth of mortality studies showing increased cardiovascular mortality in rheumatoid arthritis (RA) and the evidence suggests that the same is likely to be true of psoriatic arthritis (PsA) and ankylosing spondylitis (AS). CVD co-morbidity is due to ischaemic pathologies driven by accelerated atherosclerosis and relates to the increased prevalence and clustering of classical risk factors, which may also be affected by treatments for IA, and their interplay with novel risk factors, namely systemic inflammation. Currently we are unable to quantify the contribution that classical and novel risk factors make to an individuals' CVD risk and specific algorithms need to be developed and validated in RA, PsA and AS to facilitate clinical management. Furthermore, large clinical trials are required to assess the effect of lifestyle modifications, primary prevention strategies and effective immunosuppression on hard CVD endpoints. However, in the meantime, a pragmatic approach should be adopted towards CVD risk management. Consensus opinion has generated guidelines for the management of CVD risk in IA and we discuss the importance of assessing each individual for CVD risk and establishing a system for routine risk factor identification alongside a commitment to treat identified risk factors to specific targets.
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