Related Experiment Video
Updated: Oct 12, 2025

Author Spotlight: Self-Assessment Protocol for Predicting Psoriatic Arthritis in Psoriasis Patients
Published on: March 1, 2024
Cardiometabolic Comorbidities in Patients With Psoriasis: Focusing on Risk, Biological Therapy, and Pathogenesis
Jiangluyi Cai1,2, Lian Cui2,3, Yu Wang1,2
1Department of Dermatology, Shanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai, China.
Insights
Psoriasis patients face higher risks of cardiometabolic conditions like heart disease and diabetes. Biologic therapies can improve psoriasis and potentially reduce these associated health risks.
Area of Science:
- Dermatology and Immunology
- Cardiology and Metabolic Health
Background:
- Psoriasis is a chronic inflammatory skin condition with systemic implications.
- Significant evidence links psoriasis to increased cardiometabolic comorbidities, including cardiovascular diseases (CVDs), obesity, diabetes mellitus, and metabolic syndrome.
- The risk of these comorbidities correlates with psoriasis severity.
Purpose of the Study:
- To review the association between cardiometabolic comorbidities and psoriasis.
- To explore the benefits and precautions of biologic therapy in managing psoriasis patients with cardiometabolic comorbidities.
- To elucidate the pathogenic mechanisms underlying cardiometabolic comorbidities in psoriasis.
Main Methods:
- Review of clinical trials and existing literature.
- Analysis of pathogenic mechanisms including genetic factors, lipid metabolism, insulin resistance, and inflammatory pathways (TNF-α, IL-23/Th-17).
Main Results:
- Biologic therapies targeting inflammatory pathways show promise in improving psoriasis quality of life.
- These therapies may reduce the incidence of cardiometabolic comorbidities in psoriasis patients.
- Shared inflammatory pathways and metabolic dysregulation contribute to the comorbidity link.
Conclusions:
- Biologic therapy is a valuable tool for managing psoriasis, with potential benefits for associated cardiometabolic conditions.
- Careful consideration of benefits and precautions is essential when using biologic therapy in patients with cardiometabolic comorbidities.
- Understanding shared pathogenic mechanisms is key to comprehensive patient management.
Abstract:
Psoriasis is a chronic inflammatory disease characterized by erythematous scaly plaques, accompanied by systemic damage that leads to the development of multiple comorbidities. In particular, the association between psoriasis and cardiometabolic comorbidities, including cardiovascular diseases (CVDs), obesity, diabetes mellitus, and metabolic syndrome, has been verified in a considerable number of clinical trials. Moreover, the increased risk of cardiometabolic comorbidities positively correlates with psoriasis severity. Biologic therapy targeting inflammatory pathways or cytokines substantially improves the life quality of psoriasis patients and may affect cardiometabolic comorbidities by reducing their incidences. In this review, we focus on exploring the association between cardiometabolic comorbidities and psoriasis, and emphasize the benefits and precautions of biologic therapy in the management of psoriasis with cardiometabolic comorbidities. The pathogenic mechanisms of cardiometabolic comorbidities in psoriasis patients involve common genetic factors, lipid metabolism, insulin resistance, and shared inflammatory pathways such as tumor necrosis factor-α and interleukin-23/Th-17 pathways.
Related Concept Videos
Coronary Artery Disease I: Introduction
Atherosclerosis III: Management
Psychoneuroimmunology: Cardiovascular Disease
A key area of focus in PNI is the relationship between stress and coronary...
COPD: Pathogenesis and Clinical Features
The primary cause for the onset of COPD is cigarette smoking and exposure to air pollution. These hazardous factors initiate a chain reaction within the lungs, resulting in chronic inflammation, damage to the airways, and a...
Chronic Obstructive Pulmonary Disease-II: Pathophysiology
Chronic Inflammation
Rheumatic Heart Disease III: Medical Management

