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Published on: October 12, 2017
Psoriasis-associated vascular disease: the role of HDL
Maria Joao Paiva-Lopes1,2, José Delgado Alves3,4
1Serviço de Dermatologia, Hospital dos Capuchos CHLC, Alameda de Santo António dos Capuchos, 1169-050, Lisboa, Portugal. mjpaivalopes@sapo.pt.
Insights
Psoriasis patients show altered high-density lipoprotein (HDL) function, a key factor in cardiovascular disease risk. Biologic therapies may restore HDL structure and function, offering therapeutic potential for these patients.
Area of Science:
- Dermatology and Immunology
- Cardiovascular Medicine
- Metabolic Research
Background:
- Psoriasis is a chronic inflammatory disease affecting 2-3% of the population.
- Strong epidemiological links exist between psoriasis, cardiovascular disease (CVD), and atherosclerosis.
- CVD is the leading cause of mortality in severe psoriasis cases, even after accounting for traditional risk factors.
Purpose of the Study:
- To investigate the mechanisms underlying the increased cardiovascular risk in psoriasis patients.
- To explore alterations in lipid metabolism, specifically high-density lipoprotein (HDL) composition and function.
- To assess the impact of biologic therapy on HDL alterations in psoriasis.
Main Methods:
- Analysis of lipid metabolism and HDL parameters in psoriatic patients.
- Evaluation of HDL composition and functional assays.
- Assessment of structural and functional HDL changes following biologic therapy.
Main Results:
- Psoriatic patients exhibit significant alterations in lipid metabolism.
- Key changes observed in HDL composition and function, impacting its atheroprotective role.
- Biologic therapy demonstrated the ability to reverse both structural and functional HDL deficits.
Conclusions:
- Altered HDL function is a significant contributing mechanism to the elevated CVD risk in psoriasis.
- Biologic therapies show promise in ameliorating HDL dysfunction, suggesting a therapeutic avenue for cardiovascular complications in psoriasis.
Abstract:
Psoriasis is a chronic inflammatory systemic disease with a prevalence of 2-3%. Overwhelming evidence show an epidemiological association between psoriasis, cardiovascular disease and atherosclerosis. Cardiovascular disease is the most frequent cause of death in patients with severe psoriasis. Several cardiovascular disease classical risk factors are also increased in psoriasis but the psoriasis-associated risk persists after adjusting for other risk factors.Investigation has focused on finding explanations for these epidemiological data. Several studies have demonstrated significant lipid metabolism and HDL composition and function alterations in psoriatic patients. Altered HDL function is clearly one of the mechanisms involved, as these particles are of the utmost importance in atherosclerosis defense. Recent data indicate that biologic therapy can reverse both structural and functional HDL alterations in psoriasis, reinforcing their therapeutic potential.
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