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Published on: March 1, 2024
Cardiovascular Risk in Psoriatic Arthritis: Mechanisms, Risk Assessment, and Long-Term Management Implications
Stefan Totolici1,2, Ana-Maria Vrabie1,2, Catalin Adrian Buzea1,2
1Cardiology Department, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Insights
Psoriatic arthritis (PsA) significantly increases cardiovascular risk due to inflammation and risk factors. Managing inflammation and risk factors is crucial for reducing major adverse cardiovascular events (MACE) in PsA patients.
Area of Science:
- Rheumatology
- Cardiology
- Immunology
Background:
- Psoriatic arthritis (PsA) is a systemic immune-mediated disease.
- PsA independently elevates the risk of major adverse cardiovascular events (MACE).
- Cardiovascular risk in PsA is often underestimated in clinical practice.
Purpose of the Study:
- To review the epidemiology and pathophysiology linking PsA and cardiovascular risk.
- To provide a framework for managing cardiovascular risk in PsA patients.
- To highlight the impact of inflammation and treatment on cardiovascular outcomes.
Main Methods:
- Narrative review of recent scientific data.
- Synthesis of information on PsA, inflammation, and cardiovascular disease.
- Analysis of the effects of PsA treatments on cardiovascular risk.
Main Results:
- Chronic inflammation in PsA drives metabolic abnormalities and accelerates atherosclerosis.
- Tumor necrosis factor-α (TNF-α) inhibitors may reduce cardiovascular risk.
- Janus kinase (JAK) inhibitors require careful consideration due to potential side effects.
Conclusions:
- A multidisciplinary approach is essential for managing cardiovascular risk in PsA.
- Strict control of both inflammation and traditional risk factors is necessary.
- Reducing the burden of MACE in PsA requires integrated patient management.
Abstract:
Beyond its typical synovio-entheseal manifestations, psoriatic arthritis (PsA) is a systemic immune-mediated disease that carries a substantial, independent risk of major adverse cardiovascular events (MACE). The complex interaction of chronic systemic inflammation, a high prevalence of traditional risk factors, and PsA treatment drugs results in this increased cardiovascular burden, which is commonly underestimated in cardiology practice. Adipokine balance, insulin signalling, and lipid metabolism are all impacted by cytokine-driven systemic inflammation, which promotes metabolic abnormalities and accelerated atherogenesis. PsA-specific therapy has a complex and significant effect on cardiovascular risk. While there is evidence that strong inflammation suppression with tumour necrosis factor-α (TNF-α) inhibitors may reduce cardiovascular risk, some medications, such as Janus kinase (JAK) inhibitors, should be carefully considered due to potential side effects. In order to outline the epidemiology and pathophysiology of the PsA-cardiovascular risk nexus, this narrative review synthesises recent data. It also offers a critical framework for managing cardiovascular risk in this susceptible group, advocating for a multidisciplinary approach that incorporates strict management of both inflammation and traditional risk factors to lessen the excessive burden of MACE.
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