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Updated: Dec 29, 2025

Cholesterol Efflux Assay
Published on: March 6, 2012
HDL cholesterol efflux capacity is related to disease activity in psoriatic arthritis patients
Iván Ferraz-Amaro1, María Vanesa Hernández-Hernández1, Estefanía Armas-González1
1Servicio de Reumatología, Hospital Universitario de Canarias, La Laguna, Spain.
Insights
Cholesterol efflux capacity (CEC), crucial for cardiovascular health, is not impaired in psoriatic arthritis (PsA) patients. However, higher disease activity in PsA is independently linked to reduced CEC, increasing cardiovascular risk.
Area of Science:
- Cardiovascular Science
- Rheumatology
- Lipid Metabolism
Background:
- Cholesterol efflux capacity (CEC) is a key function of high-density lipoprotein (HDL) cholesterol, vital for removing cholesterol from macrophages.
- CEC is associated with cardiovascular event risk and can be compromised during inflammatory conditions.
Purpose of the Study:
- To investigate whether CEC is impaired in patients with psoriatic arthritis (PsA).
- To determine if disease activity or other PsA-related factors explain any potential impairment in CEC.
Main Methods:
- A case-control study involving 52 PsA patients and 53 controls.
- In vitro assessment of CEC and measurement of serum lipoprotein concentrations.
- Disease activity in PsA patients was quantified using the Disease Activity Index for Psoriatic Arthritis (DAPSA).
Main Results:
- PsA patients exhibited lower levels of total cholesterol, apolipoprotein A1, and LDL cholesterol compared to controls.
- No significant difference in CEC was observed between PsA patients and controls after adjusting for cardiovascular risk factors.
- Multivariate regression analysis revealed an independent inverse association between DAPSA score and CEC (beta coefficient -0.75, p=0.023).
Conclusions:
- CEC is not globally impaired in PsA patients but is inversely associated with disease activity.
- Elevated disease activity in PsA is an independent predictor of reduced CEC, highlighting its role in accelerated atherosclerosis.
- These findings underscore the importance of managing disease activity to mitigate cardiovascular risk in PsA.
Objective:
Cholesterol efflux capacity (CEC) is the ability of high-density lipoprotein (HDL) cholesterol to accept cholesterol from macrophages. CEC is linked to cardiovascular events in the general population, and it has been shown to be disrupted in inflammatory states. The aim of this study was to establish whether CEC is impaired in PsA patients and if this could be explained by disease-related features like disease activity.
Methods:
Case-control study that encompassed 105 individuals: 52 PsA patients and 53 controls. CEC, using an in vitro assay, and lipoprotein serum concentrations were assessed in patients and controls. Disease activity in patients with PsA was measured using the Disease Activity Index for Psoriatic Arthritis (DAPSA). Multivariate analysis was performed to study the differences between CEC in patients and controls, and the relation of CEC with PsA activity-related data and lipid profile.
Results:
Total cholesterol, apolipoprotein A1, and LDL cholesterol serum levels were downregulated in PsA patients. CEC did not differ between controls and patients (17 ± 10 vs. 18 ± 2%, p = 0.15) after adjusting for traditional cardiovascular risk factors or other variations in the lipid profile related to the disease. Traditional cardiovascular risk factors, both in patients and controls, were not related to CEC. After multivariate regression analysis, the DAPSA score was inversely and independently associated with CEC (beta coefficient - 0.75 [95%CI - 1.39-- 0.11] %, p = 0.023).
Conclusion:
CEC is inversely associated with disease activity in PSA patients, reinforcing the role of disease activity as a key factor in the development of accelerated atherosclerosis in these patients.Key Points• Cholesterol efflux capacity is linked to cardiovascular events in the general population.• In patients with psoriatic arthritis, cholesterol efflux capacity is inversely associated with disease activity (beta coefficient - 0.75[95% CI - 1.39-- 0.11] %, p = 0.023).• This finding reinforces the role of disease activity as a key factor in increasing cardiovascular risk in psoriatic arthritis patients.
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