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On the use of antiangiogenetic medications for retinopathy of prematurity

[Image: see text] In contrast to the adult, the third-trimester foetus experiences one of the most intense periods of growth and maturation of its lifetime. Early development is characterized by the existence of critical periods when environmental factors effectively produce long-lasting changes. Pr...

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Autores principales: Hård, Anna-Lena, Hellström, Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206215/
https://www.ncbi.nlm.nih.gov/pubmed/21517962
http://dx.doi.org/10.1111/j.1651-2227.2011.02330.x
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author Hård, Anna-Lena
Hellström, Ann
author_facet Hård, Anna-Lena
Hellström, Ann
author_sort Hård, Anna-Lena
collection PubMed
description [Image: see text] In contrast to the adult, the third-trimester foetus experiences one of the most intense periods of growth and maturation of its lifetime. Early development is characterized by the existence of critical periods when environmental factors effectively produce long-lasting changes. Proliferative retinopathy of prematurity (ROP) is a potentially blinding disease characterized by uncontrolled retinal angiogenesis. This pathologic angiogenesis is the target for two new treatment modalities for ROP, i.e. intravitreal anti-VEGF (bevacizumab) and systemic propranolol, which are being evaluated in ongoing or planned studies. VEGF is essential for normal angiogenesis in a growing infant, and the adrenergic system is important for many organ systems and, in addition, for plasticity of the visual and olfactory systems. CONCLUSION: This viewpoint raises concerns regarding the currently studied antiangiogenetic treatments for ROP and their possible general effects on the developing preterm infant.
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spelling pubmed-32062152011-11-04 On the use of antiangiogenetic medications for retinopathy of prematurity Hård, Anna-Lena Hellström, Ann Acta Paediatr Viewpoint Articles [Image: see text] In contrast to the adult, the third-trimester foetus experiences one of the most intense periods of growth and maturation of its lifetime. Early development is characterized by the existence of critical periods when environmental factors effectively produce long-lasting changes. Proliferative retinopathy of prematurity (ROP) is a potentially blinding disease characterized by uncontrolled retinal angiogenesis. This pathologic angiogenesis is the target for two new treatment modalities for ROP, i.e. intravitreal anti-VEGF (bevacizumab) and systemic propranolol, which are being evaluated in ongoing or planned studies. VEGF is essential for normal angiogenesis in a growing infant, and the adrenergic system is important for many organ systems and, in addition, for plasticity of the visual and olfactory systems. CONCLUSION: This viewpoint raises concerns regarding the currently studied antiangiogenetic treatments for ROP and their possible general effects on the developing preterm infant. Blackwell Publishing Ltd 2011-08 /pmc/articles/PMC3206215/ /pubmed/21517962 http://dx.doi.org/10.1111/j.1651-2227.2011.02330.x Text en Acta Pædiatrica © 2011 Foundation Acta Pædiatrica http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Viewpoint Articles
Hård, Anna-Lena
Hellström, Ann
On the use of antiangiogenetic medications for retinopathy of prematurity
title On the use of antiangiogenetic medications for retinopathy of prematurity
title_full On the use of antiangiogenetic medications for retinopathy of prematurity
title_fullStr On the use of antiangiogenetic medications for retinopathy of prematurity
title_full_unstemmed On the use of antiangiogenetic medications for retinopathy of prematurity
title_short On the use of antiangiogenetic medications for retinopathy of prematurity
title_sort on the use of antiangiogenetic medications for retinopathy of prematurity
topic Viewpoint Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206215/
https://www.ncbi.nlm.nih.gov/pubmed/21517962
http://dx.doi.org/10.1111/j.1651-2227.2011.02330.x
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