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Influence of ranibizumab treatment on the extracellular matrix in patients with neovascular age-related macular degeneration

BACKGROUND: We know the influence of the intravitreal anti-vascular endothelial growth factor (VEGF) injections on the choroidal neovascularization in the course of exudative age-related macular degeneration (AMD). However, the influence of the ranibizumab therapy in question on the extracellular ma...

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Autores principales: Nita, Małgorzata, Michalska-Małecka, Katarzyna, Mazurek, Urszula, Kimsa, Małgorzata, Strzałka-Mrozik, Barbara, Grzybowski, Andrzej, Romaniuk, Dorota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049949/
https://www.ncbi.nlm.nih.gov/pubmed/24866589
http://dx.doi.org/10.12659/MSM.890031
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author Nita, Małgorzata
Michalska-Małecka, Katarzyna
Mazurek, Urszula
Kimsa, Małgorzata
Strzałka-Mrozik, Barbara
Grzybowski, Andrzej
Romaniuk, Dorota
author_facet Nita, Małgorzata
Michalska-Małecka, Katarzyna
Mazurek, Urszula
Kimsa, Małgorzata
Strzałka-Mrozik, Barbara
Grzybowski, Andrzej
Romaniuk, Dorota
author_sort Nita, Małgorzata
collection PubMed
description BACKGROUND: We know the influence of the intravitreal anti-vascular endothelial growth factor (VEGF) injections on the choroidal neovascularization in the course of exudative age-related macular degeneration (AMD). However, the influence of the ranibizumab therapy in question on the extracellular matrix (ECM) remains unknown. We aimed to estimate the influence of Lucentis intravitreal injections on the gene expression of structural components of the extracellular matrix in patients with neovascular AMD. MATERIAL/METHODS: Patients with subfoveal localization of neovascularization in AMD, which was clinically active and observed using optical coherence tomography, were treated with ranibizumab (0.5 mg/0.05 mL) in accordance with the PrONTO scheme. Total RNA was extracted from peripheral blood mononuclear cells, and an oligonucleotide microarray technique enabled comparison of the expression level of genes encoding collagens, elastin, and laminins in AMD patients compared to control subjects. RESULTS: After 3 intravitreal injections of ranibizumab (Lucentis), COL1A1 and COL6A1 genes showed increased expression, whereas decreased expression mainly occurred for the following genes: COL4A5, COL11A1, COL4A6, LAMB4, and LAMC2. CONCLUSIONS: Anti-VEGF local therapy influences the gene expression of structural components of the ECM as measured from blood samples. The loading dose of ranibizumab for the retina changes the expression of collagen and laminin genes, but does not influence the expression of the elastin gene.
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spelling pubmed-40499492014-06-10 Influence of ranibizumab treatment on the extracellular matrix in patients with neovascular age-related macular degeneration Nita, Małgorzata Michalska-Małecka, Katarzyna Mazurek, Urszula Kimsa, Małgorzata Strzałka-Mrozik, Barbara Grzybowski, Andrzej Romaniuk, Dorota Med Sci Monit Clinical Research BACKGROUND: We know the influence of the intravitreal anti-vascular endothelial growth factor (VEGF) injections on the choroidal neovascularization in the course of exudative age-related macular degeneration (AMD). However, the influence of the ranibizumab therapy in question on the extracellular matrix (ECM) remains unknown. We aimed to estimate the influence of Lucentis intravitreal injections on the gene expression of structural components of the extracellular matrix in patients with neovascular AMD. MATERIAL/METHODS: Patients with subfoveal localization of neovascularization in AMD, which was clinically active and observed using optical coherence tomography, were treated with ranibizumab (0.5 mg/0.05 mL) in accordance with the PrONTO scheme. Total RNA was extracted from peripheral blood mononuclear cells, and an oligonucleotide microarray technique enabled comparison of the expression level of genes encoding collagens, elastin, and laminins in AMD patients compared to control subjects. RESULTS: After 3 intravitreal injections of ranibizumab (Lucentis), COL1A1 and COL6A1 genes showed increased expression, whereas decreased expression mainly occurred for the following genes: COL4A5, COL11A1, COL4A6, LAMB4, and LAMC2. CONCLUSIONS: Anti-VEGF local therapy influences the gene expression of structural components of the ECM as measured from blood samples. The loading dose of ranibizumab for the retina changes the expression of collagen and laminin genes, but does not influence the expression of the elastin gene. International Scientific Literature, Inc. 2014-05-28 /pmc/articles/PMC4049949/ /pubmed/24866589 http://dx.doi.org/10.12659/MSM.890031 Text en © Med Sci Monit, 2014 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License
spellingShingle Clinical Research
Nita, Małgorzata
Michalska-Małecka, Katarzyna
Mazurek, Urszula
Kimsa, Małgorzata
Strzałka-Mrozik, Barbara
Grzybowski, Andrzej
Romaniuk, Dorota
Influence of ranibizumab treatment on the extracellular matrix in patients with neovascular age-related macular degeneration
title Influence of ranibizumab treatment on the extracellular matrix in patients with neovascular age-related macular degeneration
title_full Influence of ranibizumab treatment on the extracellular matrix in patients with neovascular age-related macular degeneration
title_fullStr Influence of ranibizumab treatment on the extracellular matrix in patients with neovascular age-related macular degeneration
title_full_unstemmed Influence of ranibizumab treatment on the extracellular matrix in patients with neovascular age-related macular degeneration
title_short Influence of ranibizumab treatment on the extracellular matrix in patients with neovascular age-related macular degeneration
title_sort influence of ranibizumab treatment on the extracellular matrix in patients with neovascular age-related macular degeneration
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049949/
https://www.ncbi.nlm.nih.gov/pubmed/24866589
http://dx.doi.org/10.12659/MSM.890031
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