Artery Research

Volume 5, Issue 4, December 2011, Pages 197 - 197

P11.18 DETERMINANTS OF SUBCLINICAL ORGAN DAMAGE IN PAEDIATRIC KIDNEY TRANSPLANT RECIPIENTS

Authors
É. Kis1, O. Cseprekál1, A. Kerti1, T. Horváth2, A.J. Szabó1, M. Kollai2, G.S. Reusz1
11st Department of Pediatrics, Semmelweis University, Budapest, Hungary
2Clinical Experimental Research and Institute of Human Physiology, Semmelweis University, Budapest, Hungary
Available Online 29 November 2011.
DOI
10.1016/j.artres.2011.10.174How to use a DOI?
Open Access
This is an open access article distributed under the CC BY-NC license.

Increased cardiovascular (CV) risk caused by uraemic milieu decreases after kidney transplantation (Tx), however it remains 5 fold higher than in the general population. CV mortality can be characterized by non-invasive measure of arterial stiffness (Ast). (Pulse Wave Velocity (PWV), distensibility (D), and Intima media thickness (IMT)) Clinical studies on arterial wall damage in kidney transplant children are sparse.

Our aim was to evaluate the Ast parameters and the possible pathophysiological factors responsible for impaired arterial function among kidney Tx patients. PWV, D and IMT of 24 Tx children (age: 16.6±4.9 years) were measured by applanation tonometry, and carotid artery ultrasound. Laboratory values of lipid, calcium phosphate metabolism, and renal function were also assessed at the time of measurements and retrospectively one year after Tx.

PWV SDS of Tx showed a tendency of discrete elevation (0.97±0.71), IMT was above the 95th percentile (1.64±1,36). D SDS was in the normal range (−0.01±0.98). Compared to the controls PWV SDS showed positive correlation with creatinine, P, CaxP (r=0.51;r=0.4;r=0.46; p<0–05). P, CaxP values were significantly higher in Tx with IMT >95th percentile (0.13 vs. 2.61) one year after tx. (P 1.24 vs. 1.63 mmol/l; CaxP:3.19 vs 4.18 mmol2/l2).

To conclude, 4.5 years after Tx, both morphological and functional changes can occur. Disturbances of calcium phosphate metabolism can enhance the progression of athero- and arteriosclerosis, thus the impairment of arterial elastic function in children after transplantation.

Supported by: OTKA 71730, ETT 06-123/2009, TÁMOP-4.2.2-08/1/KMR-2008-0004

Journal
Artery Research
Volume-Issue
5 - 4
Pages
197 - 197
Publication Date
2011/11/29
ISSN (Online)
1876-4401
ISSN (Print)
1872-9312
DOI
10.1016/j.artres.2011.10.174How to use a DOI?
Open Access
This is an open access article distributed under the CC BY-NC license.

Cite this article

TY  - JOUR
AU  - É. Kis
AU  - O. Cseprekál
AU  - A. Kerti
AU  - T. Horváth
AU  - A.J. Szabó
AU  - M. Kollai
AU  - G.S. Reusz
PY  - 2011
DA  - 2011/11/29
TI  - P11.18 DETERMINANTS OF SUBCLINICAL ORGAN DAMAGE IN PAEDIATRIC KIDNEY TRANSPLANT RECIPIENTS
JO  - Artery Research
SP  - 197
EP  - 197
VL  - 5
IS  - 4
SN  - 1876-4401
UR  - https://doi.org/10.1016/j.artres.2011.10.174
DO  - 10.1016/j.artres.2011.10.174
ID  - Kis2011
ER  -