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Visfatin versus Flow-Mediated Dilatation as a Marker of Endothelial Dysfunction in Pediatric Renal Transplant Recipients

BACKGROUND: Renal transplantation (RTx) is the treatment of choice for paediatric end-stage renal disease (ESRD). A major cause of morbidity and mortality after RTx is cardiovascular disease. Independent predictors of cardiovascular events were shown to constitute an endothelial dysfunction (ED). Th...

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Autores principales: Fadel, Fatina, Bazraa, Hafez M., Abdelrahman, Safaa M., Shouman, Mohamed Gamal, Sayed, Marwa Khaled, Salah, Doaa Mohamed, Wahby, Aliaa Ahmed, Elgebaly, Heba F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: ID Design 2012/DOOEL Skopje 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420778/
https://www.ncbi.nlm.nih.gov/pubmed/28507632
http://dx.doi.org/10.3889/oamjms.2017.032
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author Fadel, Fatina
Bazraa, Hafez M.
Abdelrahman, Safaa M.
Shouman, Mohamed Gamal
Sayed, Marwa Khaled
Salah, Doaa Mohamed
Wahby, Aliaa Ahmed
Elgebaly, Heba F.
author_facet Fadel, Fatina
Bazraa, Hafez M.
Abdelrahman, Safaa M.
Shouman, Mohamed Gamal
Sayed, Marwa Khaled
Salah, Doaa Mohamed
Wahby, Aliaa Ahmed
Elgebaly, Heba F.
author_sort Fadel, Fatina
collection PubMed
description BACKGROUND: Renal transplantation (RTx) is the treatment of choice for paediatric end-stage renal disease (ESRD). A major cause of morbidity and mortality after RTx is cardiovascular disease. Independent predictors of cardiovascular events were shown to constitute an endothelial dysfunction (ED). This study aims to evaluate Visfatin serum level in comparison to brachial artery flow-mediated dilatation (FMD) as a marker of endothelial dysfunction in paediatric RTx recipients. METHODS: Visfatin serum level has been evaluated in 30 patients on regular hemodialysis (HD), 36 patients post-RTx and 30 controls as a measure for ED, and has been compared to brachial artery FMD. RESULTS: Visfatin level in transplant recipients was significantly lower than the hemodialysis group as well as FMD was better in transplant recipients. In spite of marked improvement of FMD and marked reduction of visfatin in post-RTx no direct statistical correlation was found between serum Visfatin level and flow-mediated dilatation. CONCLUSION: Pediatric RTx recipients show lower serum Visfatin level and better FMD than those on regular hemodialysis, reflecting less endothelial dysfunction (ED) and less cardiovascular risk. FMD in kidney transplant recipients tends to be less than normal subjects while visfatin level of the same group is similar to controls. Pediatric RTx appears to have a positive impact on the growth development of children with ESRD.
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spelling pubmed-54207782017-05-15 Visfatin versus Flow-Mediated Dilatation as a Marker of Endothelial Dysfunction in Pediatric Renal Transplant Recipients Fadel, Fatina Bazraa, Hafez M. Abdelrahman, Safaa M. Shouman, Mohamed Gamal Sayed, Marwa Khaled Salah, Doaa Mohamed Wahby, Aliaa Ahmed Elgebaly, Heba F. Open Access Maced J Med Sci Clinical Science BACKGROUND: Renal transplantation (RTx) is the treatment of choice for paediatric end-stage renal disease (ESRD). A major cause of morbidity and mortality after RTx is cardiovascular disease. Independent predictors of cardiovascular events were shown to constitute an endothelial dysfunction (ED). This study aims to evaluate Visfatin serum level in comparison to brachial artery flow-mediated dilatation (FMD) as a marker of endothelial dysfunction in paediatric RTx recipients. METHODS: Visfatin serum level has been evaluated in 30 patients on regular hemodialysis (HD), 36 patients post-RTx and 30 controls as a measure for ED, and has been compared to brachial artery FMD. RESULTS: Visfatin level in transplant recipients was significantly lower than the hemodialysis group as well as FMD was better in transplant recipients. In spite of marked improvement of FMD and marked reduction of visfatin in post-RTx no direct statistical correlation was found between serum Visfatin level and flow-mediated dilatation. CONCLUSION: Pediatric RTx recipients show lower serum Visfatin level and better FMD than those on regular hemodialysis, reflecting less endothelial dysfunction (ED) and less cardiovascular risk. FMD in kidney transplant recipients tends to be less than normal subjects while visfatin level of the same group is similar to controls. Pediatric RTx appears to have a positive impact on the growth development of children with ESRD. ID Design 2012/DOOEL Skopje 2017-04-13 /pmc/articles/PMC5420778/ /pubmed/28507632 http://dx.doi.org/10.3889/oamjms.2017.032 Text en Copyright: © 2017 Fatina Fadel, Hafez M. Bazraa, Safaa M. Abdelrahman, Mohamed Gamal Shouman, Marwa Khaled Sayed, Doaa Mohamed Salah, Aliaa Ahmed Wahby, Heba F. Elgebaly. http://creativecommons.org/licenses/CC BY-NC/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).
spellingShingle Clinical Science
Fadel, Fatina
Bazraa, Hafez M.
Abdelrahman, Safaa M.
Shouman, Mohamed Gamal
Sayed, Marwa Khaled
Salah, Doaa Mohamed
Wahby, Aliaa Ahmed
Elgebaly, Heba F.
Visfatin versus Flow-Mediated Dilatation as a Marker of Endothelial Dysfunction in Pediatric Renal Transplant Recipients
title Visfatin versus Flow-Mediated Dilatation as a Marker of Endothelial Dysfunction in Pediatric Renal Transplant Recipients
title_full Visfatin versus Flow-Mediated Dilatation as a Marker of Endothelial Dysfunction in Pediatric Renal Transplant Recipients
title_fullStr Visfatin versus Flow-Mediated Dilatation as a Marker of Endothelial Dysfunction in Pediatric Renal Transplant Recipients
title_full_unstemmed Visfatin versus Flow-Mediated Dilatation as a Marker of Endothelial Dysfunction in Pediatric Renal Transplant Recipients
title_short Visfatin versus Flow-Mediated Dilatation as a Marker of Endothelial Dysfunction in Pediatric Renal Transplant Recipients
title_sort visfatin versus flow-mediated dilatation as a marker of endothelial dysfunction in pediatric renal transplant recipients
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420778/
https://www.ncbi.nlm.nih.gov/pubmed/28507632
http://dx.doi.org/10.3889/oamjms.2017.032
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