Psoriasis strikes back! Epicardial adipose tissue: another contributor to the higher cardiovascular risk in psoriasis
1Department of Dermatology, Centro Hospitalar do Porto, Portugal.
Insights
Psoriasis is now understood as a systemic inflammatory disease linked to heart issues. Increased epicardial adipose tissue in psoriasis patients may further elevate cardiovascular risk beyond inflammation.
Area of Science:
- Immunology
- Cardiology
- Dermatology
Background:
- Psoriasis, once viewed as a skin-only inflammatory condition, is now recognized as a systemic immune-mediated disease.
- It is frequently associated with cardiometabolic diseases and increased cardiovascular mortality.
- Psoriasis may independently contribute to atherosclerosis due to its inflammatory burden.
Purpose of the Study:
- To explore the link between psoriasis and cardiovascular disease beyond systemic inflammation.
- To investigate the role of epicardial adipose tissue (EAT) as a potential contributor to cardiovascular risk in psoriasis.
Main Methods:
- Review of recent studies on psoriasis, cardiovascular disease, and EAT.
- Analysis of the association between increased EAT in psoriasis patients and subclinical atherosclerosis.
Main Results:
- Epicardial adipose tissue has been found to be increased in psoriasis patients.
- Elevated EAT in psoriasis is associated with subclinical atherosclerosis.
- The increase in EAT is likely multifactorial, involving genetic, immune, and behavioral factors.
Conclusions:
- Epicardial adipose tissue represents a novel link between psoriasis and atherosclerosis.
- Increased EAT, alongside cardiometabolic risk factors and systemic inflammation, contributes to the heightened cardiovascular risk in psoriasis patients.
Abstract:
For many years psoriasis was considered an inflammatory condition restricted to the skin. However, nowadays it is considered an immune-mediated, systemic inflammatory condition associated with numerous medical comorbidities, particularly cardiometabolic diseases, and overall cardiovascular mortality. Several studies have suggested that psoriasis may be an independent risk factor for atherosclerosis, indicating that psoriasis itself poses an intrinsic risk for cardiovascular disease, probably due to the disease's inflammatory burden. However, other causes beyond systemic inflammation and traditional cardiovascular risk factors may be implicated in cardiovascular disease in psoriasis. Recently, epicardial adipose tissue, an emerging cardiovascular risk factor, has been shown to be increased in psoriasis patients and to be associated with subclinical atherosclerosis, providing another possible link between psoriasis and atherosclerosis. The reason for the increase in epicardial adipose tissue in patients with psoriasis is unknown, but it is probably multifactorial, with genetic, immune-mediated and behavioral factors having a role. Thus, along with the increased prevalence of cardiometabolic risk factors and systemic inflammation in psoriasis, epicardial adipose tissue is probably another important contributor to the higher cardiovascular risk observed in psoriasis.
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