Markers of endothelial damage in patients with chronic kidney disease on hemodialysis

Andrés Carmona(Instituto de Salud Carlos III), M.L. Agüera(Instituto de Salud Carlos III), Carlos Luna-Ruiz(Instituto de Salud Carlos III), Paula Buendía(Instituto de Salud Carlos III), Laura Calleros(Universidad de Alcalá), Andrea García‐Jérez(Universidad de Alcalá), Manuel Rodrı́guez-Puyol(Universidad de Alcalá), Manuel Arias(Instituto de Salud Carlos III), Marta Arias‐Guillén(Instituto de Salud Carlos III), Gabriel de Arriba(Universidad de Alcalá), José Ballarín(Instituto de Salud Carlos III), Carmen Bernis(Instituto de Salud Carlos III), Elvira Fernández(Instituto de Salud Carlos III), Sagrario García-Rebollo(Universidad de La Laguna), J. García Mancha(Instituto de Salud Carlos III), Gloria del Peso(Hospital Universitario La Paz), Estefanía Pérez(Universidad de La Laguna), Esteban Poch(Instituto de Salud Carlos III), José Pórtoles(Instituto de Salud Carlos III), Diego Rodrı́guez-Puyol(Instituto de Salud Carlos III), Rafáel Sánchez(Hospital Universitario La Paz), F Sarró(Instituto de Salud Carlos III), Armando Torres(Universidad de La Laguna), Alejandro Martín‐Malo(Instituto de Salud Carlos III), Pedro Aljama(Instituto de Salud Carlos III), Rafael Ramı́rez(Universidad de Alcalá), Julia Carracedo(Universidad Complutense de Madrid)
American Journal of Physiology-Renal Physiology
January 11, 2017
Cited by 42Open Access
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Abstract

Patients with Stage 5 chronic kidney disease who are on hemodialysis (HD) remain in a chronic inflammatory state, characterized by the accumulation of uremic toxins that induce endothelial damage and cardiovascular disease (CVD). Our aim was to examine microvesicles (MVs), monocyte subpopulations, and angiopoietins (Ang) to identify prognostic markers in HD patients with or without diabetes mellitus (DM). A total of 160 prevalent HD patients from 10 centers across Spain were obtained from the Biobank of the Nephrology Renal Network (Madrid, Spain): 80 patients with DM and 80 patients without DM who were matched for clinical and demographic criteria. MVs from plasma and several monocyte subpopulations (CD14 2+ /CD16 + , CD14 + /CD16 2+ ) were analyzed by flow cytometry, and the plasma concentrations of Ang1 and Ang2 were quantified by ELISA. Data on CVD were gathered over the 5.5 yr after these samples were obtained. MV level, monocyte subpopulations (CD14 + /CD16 2+ and CD14 2+ /CD16 + ), and Ang2-to-Ang1 ratios increased in HD patients with DM compared with non-DM patients. Moreover, MV level above the median (264 MVs/µl) was associated independently with greater mortality. MVs, monocyte subpopulations, and Ang2-to-Ang1 ratio can be used as predictors for CVD. In addition, MV level has a potential predictive value in the prevention of CVD in HD patients. These parameters undergo more extensive changes in patients with DM.


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