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NDT Advance Access published online on January 10, 2008

Nephrology Dialysis Transplantation, doi:10.1093/ndt/gfm943
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© The Author [2008]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org



Association between endothelial progenitor cell depletion in blood and mild-to-moderate renal insufficiency in stable angina

Andrzej Surdacki1, Ewa Marewicz2, Ewa Wieteska1, Grzegorz Szastak1, Tomasz Rakowski1, Ewa Wieczorek-Surdacka3, Dariusz Dudek1, Juliusz Pryjma2 and Jacek S. Dubiel1

1 2nd Department of Cardiology, Jagiellonian University, Cracow, Poland 2 Department of Immunology, Jagiellonian University, Cracow, Poland 3 Department of Nephrology, Jagiellonian University, Cracow, Poland

Correspondence and offprint requests to: Andrzej Surdacki, 2nd Department of Cardiology, Jagiellonian University, 17 Kopernika Street, 31-501 Cracow, Poland. Tel/Fax: +48-12-636-8039; E-mail: surdacki.andreas{at}gmx.net



  Abstract

Background. Low blood counts of CD34/kinase-insert domain receptor double-positive cells (CD34+/KDR+ cells)—a leukocytes subpopulation enriched for bone marrow-derived endothelial progenitor cells (EPC)— predict adverse outcomes in coronary artery disease (CAD). The dependence of EPC numbers on the glomerular filtration rate (GFR), another prognostic factor, has not been reported in CAD yet. Our aim was to assess CD34+/KDR+ cell counts versus GFR in stable angina.

Methods. We studied 102 stable angina men with severe angiographic CAD and normal left-ventricular systolic function. CD34+/KDR+ cells were enumerated by flow cytometry.

Results. With lowering GFR, CD34+/KDR+ cell numbers (% of lymphocytes, median and interquartile range) decreased: 0.04 (0.03–0.06), 0.03 (0.02–0.05) and 0.02 (0.01–0.03)% for GFR ≥90, 60–89 and 30–59 ml/min/1.73 m2, respectively (P < 0.001 for trend). CD34+/KDR+ cell counts correlated with GFR (r = 0.25, P = 0.01), CAD extension score (r = –0.20, P = 0.04), soluble form of vascular cell adhesion molecule-1 (sVCAM-1) (r = –0.22, P = 0.03) and homocysteine (r = –0.20, P = 0.04) levels. A GFR <90 ml/min/1.73 m2 was associated with insignificantly higher plasma erythropoietin concentrations (r = –0.22, P = 0.09 for trend) that correlated with haemoglobin levels (r = –0.33, P = 0.01, n = 59). The GFR–CD34+/KDR+ cells relation was attenuated, yet maintained (β = 0.19 ± 0.09, P = 0.04) on adjustment for the remaining multivariate determinants of CD34+/KDR+ cell numbers: sVCAM-1 (β = –0.20 ± 0.09, P = 0.03) and haemoglobin (β = 0.18 ± 0.09, P = 0.05).

Conclusions. Mild-to-moderate renal dysfunction accompanying stable angina is associated with CD34+/KDR+ cell depletion, which partially depends on concomitant endothelial dysfunction and a tendency to anaemia (despite insignificantly higher erythropoietin) irrespective of an angiographic CAD extent. This may exacerbate an imbalance between endothelial injury and EPC-mediated repair, thus contributing to high cardiovascular risk in CAD coexisting with renal insufficiency.

Keywords: coronary artery disease; endothelial progenitor cells; renal insufficiency

Received for publication: 14. 9.07
Accepted in revised form: 19.12.07


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