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Increased circulating endothelial cells and microparticles in patients with psoriasis
Vicenta Martínez-Sales1, Virtudes Vila1, José M Ricart2
1Research Center, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Clinical Hemorheology and Microcirculation
|September 5, 2013
Summary
Psoriasis patients exhibit elevated circulating endothelial cells (CECs) and microparticles (MPs), indicating endothelial dysfunction. These markers correlate with inflammation, atherosclerosis, and microcirculation changes in psoriasis.
Area of Science:
- Vascular Biology
- Dermatology
- Inflammation Research
Background:
- Psoriasis is a chronic inflammatory disease linked to vascular endothelium alterations.
- Endothelial dysfunction is a key factor in psoriasis pathogenesis.
- Quantifying circulating endothelial cells (CECs) and microparticles (MPs) may reveal disease mechanisms.
Purpose of the Study:
- To measure CECs and MPs in psoriasis patients.
- To investigate the relationship between CECs/MPs and endothelial/inflammation markers.
- To assess correlations with subclinical atherosclerosis and microcirculation.
Main Methods:
- Study included 20 psoriasis patients and 20 controls.
- Measured circulating markers: CECs, MPs, von Willebrand factor (vWF), E-selectin (E-sel), Interleukin-6 (IL-6), C-reactive protein (CRP).
- Assessed subclinical atherosclerosis via carotid ultrasound (intima-media thickness) and microcirculation via nailfold capillaroscopy.
Main Results:
- CECs, MPs, vWF, CRP, and E-sel levels were significantly higher in psoriasis patients versus controls.
- Elevated CECs and MPs (above 99th percentile of controls) were observed in 94% and 53% of patients, respectively.
- MPs correlated with inflammatory markers and intima-media thickness; CECs correlated with capillary density.
Conclusions:
- Psoriasis patients demonstrate increased CECs and MPs, signifying endothelial dysfunction.
- Elevated CECs and MPs are associated with inflammatory markers in psoriasis.
- These findings link endothelial dysfunction markers to subclinical atherosclerosis and microcirculation changes in psoriasis.
