TITLE

Identyfikacja ekspresji liganda CD40 (CD154) na powierzchni konglomeratu płytka-monocyt u dzieci z zespołem metabolicznym

AUTHOR(S)
Urban, Mirosława; Urban, Remigiusz; Krasowska, Irena; Głowińska-Olszewska, Barbara; Stasiak-Barmuta, Anna; Bossowski, Artur; Koput, Alicja
PUB. DATE
June 2008
SOURCE
Pediatric Endocrinology, Diabetes & Metabolism;2008, Vol. 14 Issue 2, p71
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
Introduction: The increased expression of the transmembrane protein CD40 on macrophages, endothelium, smooth muscle cells, platelet-monocyte conglomerate is connected with an enlarged risk of the occurrence of diseases of the cardiovascular system in the metabolic syndrome. The aim of the study was to establish whether metabolic syndrome in children can already be a precursor of cardiovascular diseases. Material and methods: The study was carried out on 35 children aged 10-18 years with the metabolic syndrome recognized according to the National Cholesterol Educational Program Adult Treatment Panel III (ATP III) criteria. The control group consisted of 26 healthy children without risk factors. In the examined children we evaluated BMI, the blood pressure, lipids, hsCRP, and the HOMA index. The analysis of the expression CD 40L (CD154) was performed with a three-color flow cytometer. The identification surrendered 104 cells. Statistical analysis was performed with use of U-Mann-Whitney test, for correlation analysis we used Spearman and Pearson tests. Results: We observed an elevated expression of CD40 ligand on the surface on platelet-monocyte conglomerate in patients with the metabolic syndrome compared to healthy children (12.7 vs. 4.95%, p=0.0036). In addition, we found a statistically significant correlation between the expression of the CD40L and HOMA index (r = -0.33, p<0.028). Conclusions: Enlarged expression of the transmembrane protein CD40L not only initiates and influences the progression of the atherosclerosis, but modulates the architecture of atherosclerotic plaque as well.
ACCESSION #
37168208

 

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