alexa Serum Bone Markers and Coronary Artery Calcification in End Stage Renal Failure Patients and Kidney Transplant Recipients | OMICS International | Abstract
ISSN: 2161-0959

Journal of Nephrology & Therapeutics
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Research Article

Serum Bone Markers and Coronary Artery Calcification in End Stage Renal Failure Patients and Kidney Transplant Recipients

Tanja Celic1*, Josip Spanjol2, Antun Grskovic2, Melita Kukuljan3, Sanjin Racki4, Tomislav Kurelac1, Ivana Maric1 and Dragica Bobinac1

1Department of Anatomy, University Hospital Rijeka, Rijeka, Croatia

2Department of Urology, University Hospital Rijeka, Rijeka, Croatia

3Department of Radiology, University Hospital Rijeka, Rijeka, Croatia

4Department of Nephrology, University Hospital Rijeka, Rijeka, Croatia

*Corresponding Author:
Tanja Celic
Department of Anatomy, Faculty of Medicine
Brace Branchetta 20, 51 000 Rijeka, Croatia
Tel: +385 51 651 143
Fax: +385 51 651 143
E-mail: [email protected]

Received Date: November 03, 2011; Accepted Date: July 25, 2012; Published Date: July 28, 2012

Citation: Celic T, Spanjol J, Grskovic A, Kukuljan M, Racki S, et al. (2012) Serum Bone Markers and Coronary Artery Calcification in End Stage Renal Failure Patients and Kidney Transplant Recipients. J Nephrol Therapeut 2:125. doi:10.4172/2161-0959.1000125

Copyright: © 2012 Celic T, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.


Background: Variety of growth factors and cytokines are involved in the process of bone turnover. Evidences are showing that alterations in OPG/RANK/RANKL system form the basis of many metabolic diseases. So, we evaluated the relationship between OPG and RANKL levels, to establish a possible relationship with other bone markers and coronary artery calcification.
Methods: Patients with chronic kidney disease and patients during the first year after transplantation had coronary artery scan and their blood was analyzed for serum bone markers. The following serum markers were measured: OPG, RANKL, BAP, TRAP5b and iPTH.
Results: All measured bone markers values increased with the disease progression and return to normal values during the first year after transplantation. Serum values of OPG, BAP, TRAP5b and iPTH are influenced by gender, age and dialysis duration. There is a significant negative correlation between PTH and OPG, and positive between PTH, BAP and TRAP5b values. No correlation between OPG and sRANKL, or OPG/sRANKL levels with other tested markers was found. In multivariate analysis of CACS revealed that OPG is significantly correlated with calcification in entire study population. Conclusions: This study shows that increased bone turnover markers are present in chronic kidney disease but mainly depending on gender, age and dialysis duration. The effects of those factors are overridden by glucocorticoids effect in transplanted patients. The correlation of OPG with arterial calcification presents it as a possible calcification marker.
This is the first study on bone metabolism that covered Chronic Kidney Disease (CKD) patients, both predialysed and hemodialysed, as well as kidney transplant recipients. Results of our study demonstrate that serum levels of all investigated bone markers as well as calcification of coronary arteries are increased during CKD, with highest measured values in HD population.


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