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NDT Advance Access originally published online on November 4, 2007
Nephrology Dialysis Transplantation 2008 23(3):959-965; doi:10.1093/ndt/gfm727
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© The Author [2007]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org



Serum visfatin concentration and endothelial dysfunction in chronic kidney disease

Mahmut Ilker Yilmaz1,2, Mutlu Saglam3, Juan Jesus Carrero2, Abdul Rashid Qureshi2, Kayser Caglar1, Tayfun Eyileten1, Alper Sonmez4, Erdinc Cakir5, Mujdat Yenicesu1, Bengt Lindholm2, Peter Stenvinkel2 and Jonas Axelsson2

1 Departments of Nephrology, Gülhane School of Medicine, 06018 Etlik-Ankara, Turkey 2 Divisions of Renal Medicine and Baxter Novum, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, K 56 Karolinska University Hospital at Huddinge, Stockholm, Sweden 3 Departments of Radiology, Gülhane School of Medicine, 06018 Etlik-Ankara, Turkey 4 Departments of Internal Medicine, Gülhane School of Medicine, 06018 Etlik-Ankara, Turkey 5 Departments of Biochemistry, Gülhane School of Medicine, 06018 Etlik-Ankara, Turkey

Mahmut Ilker Yilmaz, Division of Renal Medicine and Baxter Novum, Department of Clinical Science, Intervention and Technology, K56 Karolinska University Hospital Huddinge, 141 86 Stockholm, Sweden. Tel: +46-8-58582532; Fax: +46-8-58582532; E-mail: mahmutiyilmaz{at}yahoo.com



  Abstract

Background. Endothelial dysfunction (ED) is common in patients with moderate to advanced chronic kidney disease (CKD). Recently, visfatin, a protein with insulin-mimetic properties, was shown to be associated with sVCAM-1. Thus, we hypothesised that visfatin may be a marker of ED in CKD.

Methods. We studied 406 patients with different stages of non-diabetic CKD (50% males, 46 ± 12 years), testing the relationship between flow-mediated dilatation (FMD), assessed by high resolution brachial ultrasonography, and plasma adiponectin and visfatin concentrations. Eighty healthy volunteers (50% males, 46 ± 11 years) served as matched controls.

Results. Compared to healthy controls, ED was observed in all stages of CKD (Stages 1–5) and correlated strongly with the reduction in estimated glomerular filtration rate (eGFR). Whereas visfatin concentrations were found to be increased in all but CKD stages 1 and 2, adiponectin levels were found to be increased in all patients but CKD stage 1. Visfatin and adiponectin levels were strongly correlated with eGFR (rho = –0.62 and rho = –0.72, respectively, P < 0.001 for both). FMD levels were negatively correlated with both visfatin and adiponectin levels (rho = –0.53 and, rho = –0.57, respectively, P < 0.001 for both). In a multiple regression model, eGFR levels (Beta = 0.74, P < 0.001), visfatin (Beta = –0.15, P < 0.001), age (Beta = 0.06, P < 0.01), adiponectin (Beta = 0.09, P < 0.05), HOMA-IR (Beta = 0.07, P < 0.05) and hsCRP (Beta = –0.08, P < 0.05) were all found to be significantly related to FMD.

Conclusions. We conclude that the circulating levels of visfatin and adiponectin are associated with ED in all stages of CKD, independently of inflammation and insulin resistance.

Keywords: adiponectin; flow-mediated dilation; insulin resistance; visfatin

Received for publication: 21. 4.07
Accepted in revised form: 18. 9.07


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