Cardiovascular

Atherogenic Lipoprotein Burden, Metabolic Stress and Immune Activation Associated with Coronary Atherosclerosis in Patients with Psoriasis.

TL;DR

Subclinical coronary atherosclerosis in patients with psoriasis is closely associated with an immuno-metabolic risk profile encompassing atherogenic lipoprotein fractions (particularly remnant cholesterol) and immune activation (elevated IgA), underscoring the need for broader cardiovascular risk assessment beyond traditional risk factors.

Key Findings

Remnant cholesterol emerged as a strong independent predictor of coronary stenosis in patients with psoriasis.

  • Patients with psoriasis (n = 104) without known coronary artery disease underwent coronary computed tomography angiography (CCTA) to detect subclinical coronary atherosclerosis.
  • Remnant cholesterol was identified as an independent predictor of coronary stenosis in multivariate logistic regression models.
  • Patients with coronary atherosclerosis exhibited a more adverse lipid profile overall compared to those without coronary atherosclerosis.
  • Lipid fractions including remnant cholesterol were analyzed alongside clinical data and metabolic parameters.

Elevated IgA levels were associated with the presence of coronary atherosclerosis in psoriasis patients, suggesting a role of immune activation beyond general systemic inflammation.

  • Immunoglobulin A (IgA) was measured as an immunological marker in the study population of 104 psoriasis patients.
  • Elevated IgA levels were associated with CT-confirmed coronary stenosis in univariate and/or multivariate logistic regression analyses.
  • The authors note this finding suggests a potential role of immune activation that 'extends beyond general systemic inflammation.'
  • IgA was included as part of a broader immuno-metabolic risk profile analysis.

Longer duration of psoriasis correlated with the presence of coronary atherosclerosis, highlighting the importance of cumulative inflammatory burden.

  • Disease duration was analyzed as a clinical variable in 104 psoriasis patients without known coronary artery disease.
  • Longer psoriasis duration was associated with CT-confirmed coronary stenosis detected by CCTA.
  • The authors describe this as reflecting 'the importance of cumulative inflammatory burden' in the pathogenesis of coronary atherosclerosis.
  • The finding was assessed using univariate and multivariate logistic regression models.

Patients with psoriasis and coronary atherosclerosis exhibited a more adverse metabolic and lipid profile compared to those without coronary atherosclerosis.

  • The study enrolled 104 psoriasis patients without known coronary artery disease who underwent CCTA.
  • Metabolic parameters and indices, lipid fractions including remnant cholesterol, and immunological markers were compared between patients with and without CT-confirmed coronary stenosis.
  • The adverse metabolic profile in those with coronary atherosclerosis encompassed multiple atherogenic lipoprotein fractions.
  • These differences were assessed using univariate and multivariate logistic regression models.

Subclinical coronary atherosclerosis was detectable by CCTA in a population of psoriasis patients without known coronary artery disease.

  • All 104 study participants had psoriasis but no known coronary artery disease prior to enrollment.
  • Coronary computed tomography angiography (CCTA) was used to detect subclinical coronary atherosclerosis and confirm coronary stenosis.
  • The study design allowed assessment of associations between clinical, metabolic, and immunological variables and CT-confirmed coronary stenosis.
  • The authors conclude that cardiovascular risk assessment in psoriasis patients should extend 'beyond the evaluation of traditional cardiovascular risk factors alone.'

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Citation

Djukanovic L, Skiljevic D, Nikolic M, Malinic M, Popadic S, Radmili O, et al.. (2026). Atherogenic Lipoprotein Burden, Metabolic Stress and Immune Activation Associated with Coronary Atherosclerosis in Patients with Psoriasis.. International journal of molecular sciences. https://doi.org/10.3390/ijms27052353