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Published on: March 1, 2024
Cardiovascular comorbidities in patients with psoriatic arthritis: a systematic review
Anna Jamnitski1, Deborah Symmons, Mike J L Peters
1Department of Rheumatology, Jan van Breemen Research Institute/READE, Dr Jan van Breemenstraat 2, 1056 AB Amsterdam, The Netherlands.
Insights
Patients with psoriatic arthritis (PsA) face increased cardiovascular risk, similar to rheumatoid arthritis. Managing inflammation and traditional risk factors is crucial for cardiovascular health in PsA patients.
Area of Science:
- Rheumatology
- Cardiology
- Epidemiology
Background:
- Limited data exists on cardiovascular comorbidity and risk factors in psoriatic arthritis (PsA).
- Understanding the cardiovascular risk profile in PsA is essential for patient management.
Purpose of the Study:
- To systematically review and summarize available studies on cardiovascular risk in patients with PsA.
- To evaluate the cardiovascular risk profile in PsA.
Main Methods:
- A systematic literature search was conducted across Medline, EMBASE, and the Cochrane library.
- Searched for English-language articles from January 1966 to April 2011.
- Excluded review articles, case reports, and studies on psoriasis alone.
Main Results:
- Twenty-eight articles were included in the review.
- PsA patients showed increased cardiovascular mortality and morbidity.
- PsA patients exhibited more prominent cardiovascular risk factors like hypertension, dyslipidemia, and obesity.
- Inflammation suppression showed a favorable effect on cardiovascular surrogate markers.
Conclusions:
- PsA is associated with an elevated cardiovascular risk, comparable to rheumatoid arthritis.
- Similar cardiovascular risk management strategies are needed for both PsA and rheumatoid arthritis.
- Further research is required to determine the impact of inflammation suppression and traditional risk factor modification on cardiovascular risk reduction in PsA.
Objective:
Data regarding cardiovascular comorbidity and cardiovascular risk factors in patients with psoriatic arthritis (PsA) are limited. To evaluate the cardiovascular risk profile, a systematic literature search was performed to provide an extensive summary of all studies available on cardiovascular risk in PsA.
Methods:
Medline, EMBASE and the Cochrane library were searched from January 1966 to April 2011 for English language articles on data concerning cardiovascular diseases and cardiovascular risk factors in PsA. Review articles, case reports and studies on psoriasis alone were excluded.
Results:
Twenty-eight articles were included in this review. Studies on all-cause mortality revealed mixed results. Available data on cardiovascular disease appeared more consistent, indicating an increased cardiovascular mortality and morbidity in PsA. Commensurate with this, surrogate markers of subclinical atherosclerosis, arterial stiffness and cardiovascular risk factors, for example hypertension, dyslipidaemia, obesity and metabolic-related factors, were more prominent in PsA compared with controls. Suppression of inflammation was linked with a favourable effect on cardiovascular surrogate markers, for example carotid intima media thickness and endothelial dysfunction, in several (un)controlled studies.
Conclusion:
Most studies point towards an increased cardiovascular risk in PsA, broadly on a par with the risk level in rheumatoid arthritis, emphasising the need for similar cardiovascular risk management in both conditions. Further studies are needed to indicate whether inflammatory suppression or modification of traditional cardiovascular risk factors, or both, will reduce cardiovascular risk.
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