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Author Spotlight: Self-Assessment Protocol for Predicting Psoriatic Arthritis in Psoriasis Patients
Published on: March 1, 2024
Double trouble: psoriasis and cardiometabolic disorders
Nasrin Goolam Mahyoodeen1, Nigel J Crowther2, Mohammed Tikly1
1Department of Internal Medicine, Chris Hani Baragwanath Academic Hospital, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Insights
Psoriasis (PsO) is linked to increased cardiometabolic disease (CMD) risk due to chronic inflammation and shared risk factors. Managing inflammation and CMD is crucial for patients with psoriasis.
Area of Science:
- Dermatology
- Cardiology
- Metabolic Diseases
Background:
- Psoriasis (PsO) is a chronic inflammatory skin condition.
- PsO is associated with numerous co-morbidities, particularly cardiometabolic diseases (CMD).
Purpose of the Study:
- To review the epidemiology and pathogenetic mechanisms linking PsO and CMD.
- To discuss factors contributing to the increased risk of cardiovascular morbidity and mortality in PsO patients.
Main Methods:
- Descriptive review of registry-based studies.
- Analysis of epidemiological data and pathogenetic mechanisms.
Main Results:
- PsO is associated with an elevated risk of cardiovascular morbidity and mortality.
- Key linking factors include chronic inflammation, obesity, traditional cardiovascular risk factors, and systemic therapies.
- Inflammation from PsO and obesity creates a pro-atherogenic environment.
Conclusions:
- Systemic therapies reducing inflammation may improve CMD in PsO patients.
- Screening for and treating CMD, alongside lifestyle modifications, are vital interventions.
- Further research is needed on the impact of systemic therapy on CMD progression.
Abstract:
Psoriasis (PsO) is a chronic immune-mediated inflammatory skin disorder associated with numerous co-morbidities. This descriptive review focuses on the cardiometabolic co-morbidities of PsO with reference to the epidemiology and pathogenetic mechanisms linking PsO and cardiometabolic disease (CMD). Registry-based studies have shown PsO to be associated with an increased risk of cardiovascular morbidity and mortality. Factors linking PsO and CMD include: chronic inflammation, obesity, classic cardiovascular risk factors, and the effects of systemic therapy used to treat PsO. Chronic inflammation is associated with PsO itself, and with obesity. Adipose tissue is responsible for the secretion of various adipokines, which together with pro-inflammatory cytokines arising from the psoriatic plaque, contribute to the pro-inflammatory and pro-atherogenic environment. Systemic therapy aimed at decreasing inflammation has been shown to improve CMD in PsO. Screening for and treating CMD and initiating lifestyle modifications will remain the most important interventions until further data emerge regarding the effect of systemic therapy on CMD progression.
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