Abstract

BackgroundVascular calcification (VC) is an independent predictor of cardiovascular disease (CVD) present in 30–70% of patients with chronic kidney disease (CKD). Copeptin is a sensitive surrogate marker of arginine vasopressin (AVP), which is involved in many pathophysiologic processes in CKD. The aim of the present study was to explore the association of copeptin with VC in CKD stage 5.MethodsCopeptin was investigated in conjunction with living donor kidney transplantation in 149 clinically stable CKD stage 5 patients (CKD5), including 53 non-dialyzed (CKD5-ND) and 96 dialysis patients treated by peritoneal dialysis (PD) (n = 43) or hemodialysis (HD) (n = 53). We analyzed the association of copeptin with presence and extent of VC ascertained both histologically in biopsies from the inferior epigastric artery (n = 137) and by coronary artery calcification (CAC) score measured by computed tomography.ResultsPatients with higher copeptin were older, had higher systolic blood pressure, higher prevalence of CVD and their preceding time on chronic dialysis was longer. In Spearman’s rank correlations (Rho), copeptin concentrations were significantly associated with CAC score (Rho = 0.27; p = 0.003) and presence of medial VC (Rho = 0.21; p = 0.016). Multivariate logistic regression analysis showed that 1-SD higher age, male gender, diabetes and 1-SD higher copeptin were significantly associated with the presence of moderate-extensive VC.ConclusionsHigh circulating levels of copeptin in CKD5 patients are independently associated with the degree of medial calcification ascertained by histology of arterial biopsies. Thus, plasma copeptin may serve as a marker of the uremic calcification process.

Highlights

  • Vascular calcification (VC) is an independent predictor of cardiovascular disease (CVD) present in 30– 70% of patients with chronic kidney disease (CKD)

  • Characteristics of the studied CKD stage 5 patients (CKD5) patients according to dialysis dependence are presented in Additional file 1: Table S1

  • There was no difference in copeptin concentration between peritoneal dialysis (PD) and HD patients (427 vs. 412 pg/mL, p = 1.0), while plasma copeptin was significantly lower in CKD5-ND patients compared to PD and HD patients (351 vs. 427 pg/mL, p = 0.02; and 351 vs. 412 pg/mL, p = 0.001, respectively)

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Summary

Introduction

Vascular calcification (VC) is an independent predictor of cardiovascular disease (CVD) present in 30– 70% of patients with chronic kidney disease (CKD). Medial calcification is predominantly related to abnormal metabolism in CKD and represents one of the uremic features entitled CKD – mineral and bone disorder (CKD-MBD) [10]. Several biomarkers, such as calcium, phosphate, alkaline phosphatase, parathyroid hormone, fibroblast growth factor–23 (FGF-23), Klotho, vitamin D3, osteoprotegerin (OPG) and sclerostin, play important roles in pathological pathways of CKD-BMD [11,12,13], the exact pathogenic mechanisms remain unclear and additional factors are likely to be involved

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