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Reduced Vitamin D Receptor on Circulating Endothelial Progenitor Cells: A New Risk Factor of Coronary Artery Diseases

Aim: Endothelial progenitor cells (EPCs) are shown to participate in the pathological processes of atherosclerosis. While Vitamin D and its receptor axis might exert some effects on EPCs' function. But their exact relationship with clinical patients is still elusive, which inspired us to explor...

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Detalles Bibliográficos
Autores principales: Ai, Sidi, He, Zhiqing, Ding, Ru, Wu, Feng, Huang, Zhigang, Wang, Jiamei, Huang, Shuaibo, Dai, Xianliang, Zhang, Jiayou, Chen, Jing, Liu, Linlin, Wu, Zonggui, Liang, Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japan Atherosclerosis Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945554/
https://www.ncbi.nlm.nih.gov/pubmed/29176261
http://dx.doi.org/10.5551/jat.40808
Descripción
Sumario:Aim: Endothelial progenitor cells (EPCs) are shown to participate in the pathological processes of atherosclerosis. While Vitamin D and its receptor axis might exert some effects on EPCs' function. But their exact relationship with clinical patients is still elusive, which inspired us to explore the potential association of vitamin D receptor (VDR) expression on circulating EPCs and serum vitamin D levels among patients with coronary artery disease (CAD). Methods: Two hundred patients with CAD after their admission to hospital and one hundred healthy controls were enrolled. Medical history data were retrieved and fresh blood samples were collected for flow cytometry analysis. VDR expressions on EPCs were evaluated according to the standardized protocol. Logistic regression analysis was used to investigate the potential risk factor of CAD. Results: CAD patients were found to have lower log(10)(VDR-MFIs) than those of control group, especially for patients with diabetes (p < 0.001). Log(10)(VDR-MFIs) were inversely correlated with glycated hemoglobin (R = −0.472, p < 0.001), and while EPCs challenged with high glucose had lower VDR expression. Multivariate logistic regression analysis revealed that lower log(10)(VDR-MFIs) were independently associated with the risk of CAD (OR = 0.055, p = 0.008). Conclusion: A significant decrease of VDR expression on circulating EPCs was observed among CAD patients, particularly among those also with diabetes. VDR expression on EPCs was independently negatively correlated with HbA(1c) and high glucose decreased EPCs' VDR expression. Low levels of VDR expression on circulating EPCs might serve as a potential risk factor of CAD.