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Vascular endothelial growth factor in children with cyanotic and acyanotic and congenital heart disease
INTRODUCTION: Vascular endothelial growth factor is a potent stimulator of angiogenesis. Children with cyanotic congenital heart disease often experience the development of widespread formation of collateral blood vessels, which may represent a form of abnormal angiogenesis resulting in increased mo...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281344/ https://www.ncbi.nlm.nih.gov/pubmed/22371751 http://dx.doi.org/10.5114/aoms.2010.13899 |
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author | Baghdady, Yasser Hussein, Yasser Shehata, Mohamed |
author_facet | Baghdady, Yasser Hussein, Yasser Shehata, Mohamed |
author_sort | Baghdady, Yasser |
collection | PubMed |
description | INTRODUCTION: Vascular endothelial growth factor is a potent stimulator of angiogenesis. Children with cyanotic congenital heart disease often experience the development of widespread formation of collateral blood vessels, which may represent a form of abnormal angiogenesis resulting in increased morbidity and mortality. We undertook the present study to determine whether children with cyanotic congenital heart disease have elevated serum levels of vascular endothelial growth factor compared to children with acyanotic heart disease. MATERIAL AND METHODS: Serum was obtained from 35 children with cyanotic congenital heart disease and 30 children with acyanotic heart disease. Vascular endothelial growth factor levels were measured in the serum of these patients by sandwich enzyme immunoassay. RESULTS: Vascular endothelial growth factor was significantly elevated in children with cyanotic congenital heart disease compared to children with acyanotic heart disease (150.3 ±48.1 vs. 85.4 ±18.7 pg/ml, respectively, p < 0.001). In the cyanotic group, oxygen saturation (SaO(2)) was negatively correlated with VEGF (r=–0.631, p < 0.001) while haemoglobin was positively correlated (r=0.781, p = 0.007). No significant correlations were found in the acyanotic group. CONCLUSIONS: Children with cyanotic congenital heart disease have elevated systemic levels of vascular endothelial growth factor directly related to the degree of cyanosis (SaO(2) and haemoglobin levels). These findings suggest that the widespread formation of collateral vessels in these children may be mediated by vascular endothelial growth factor. |
format | Online Article Text |
id | pubmed-3281344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-32813442012-02-27 Vascular endothelial growth factor in children with cyanotic and acyanotic and congenital heart disease Baghdady, Yasser Hussein, Yasser Shehata, Mohamed Arch Med Sci Original Research INTRODUCTION: Vascular endothelial growth factor is a potent stimulator of angiogenesis. Children with cyanotic congenital heart disease often experience the development of widespread formation of collateral blood vessels, which may represent a form of abnormal angiogenesis resulting in increased morbidity and mortality. We undertook the present study to determine whether children with cyanotic congenital heart disease have elevated serum levels of vascular endothelial growth factor compared to children with acyanotic heart disease. MATERIAL AND METHODS: Serum was obtained from 35 children with cyanotic congenital heart disease and 30 children with acyanotic heart disease. Vascular endothelial growth factor levels were measured in the serum of these patients by sandwich enzyme immunoassay. RESULTS: Vascular endothelial growth factor was significantly elevated in children with cyanotic congenital heart disease compared to children with acyanotic heart disease (150.3 ±48.1 vs. 85.4 ±18.7 pg/ml, respectively, p < 0.001). In the cyanotic group, oxygen saturation (SaO(2)) was negatively correlated with VEGF (r=–0.631, p < 0.001) while haemoglobin was positively correlated (r=0.781, p = 0.007). No significant correlations were found in the acyanotic group. CONCLUSIONS: Children with cyanotic congenital heart disease have elevated systemic levels of vascular endothelial growth factor directly related to the degree of cyanosis (SaO(2) and haemoglobin levels). These findings suggest that the widespread formation of collateral vessels in these children may be mediated by vascular endothelial growth factor. Termedia Publishing House 2010-04-30 2010-04-30 /pmc/articles/PMC3281344/ /pubmed/22371751 http://dx.doi.org/10.5114/aoms.2010.13899 Text en Copyright © 2010 Termedia & Banach http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Baghdady, Yasser Hussein, Yasser Shehata, Mohamed Vascular endothelial growth factor in children with cyanotic and acyanotic and congenital heart disease |
title | Vascular endothelial growth factor in children with cyanotic and acyanotic and congenital heart disease |
title_full | Vascular endothelial growth factor in children with cyanotic and acyanotic and congenital heart disease |
title_fullStr | Vascular endothelial growth factor in children with cyanotic and acyanotic and congenital heart disease |
title_full_unstemmed | Vascular endothelial growth factor in children with cyanotic and acyanotic and congenital heart disease |
title_short | Vascular endothelial growth factor in children with cyanotic and acyanotic and congenital heart disease |
title_sort | vascular endothelial growth factor in children with cyanotic and acyanotic and congenital heart disease |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281344/ https://www.ncbi.nlm.nih.gov/pubmed/22371751 http://dx.doi.org/10.5114/aoms.2010.13899 |
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