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Cell surgery and growth factors in dry age-related macular degeneration: visual prognosis and morphological study

BACKGROUND: The aim of this research was to study the overall restoration effect on residual retinal cells through surgically grafted autologous cells onto the surrounding tissue, choroid and retina in order to produce a constant secretion of growth factors (GFs) in dry age-related macular degenerat...

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Autores principales: Limoli, Paolo Giuseppe, Limoli, Celeste, Vingolo, Enzo Maria, Scalinci, Sergio Zaccaria, Nebbioso, Marcella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216913/
https://www.ncbi.nlm.nih.gov/pubmed/27391437
http://dx.doi.org/10.18632/oncotarget.10442
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author Limoli, Paolo Giuseppe
Limoli, Celeste
Vingolo, Enzo Maria
Scalinci, Sergio Zaccaria
Nebbioso, Marcella
author_facet Limoli, Paolo Giuseppe
Limoli, Celeste
Vingolo, Enzo Maria
Scalinci, Sergio Zaccaria
Nebbioso, Marcella
author_sort Limoli, Paolo Giuseppe
collection PubMed
description BACKGROUND: The aim of this research was to study the overall restoration effect on residual retinal cells through surgically grafted autologous cells onto the surrounding tissue, choroid and retina in order to produce a constant secretion of growth factors (GFs) in dry age-related macular degeneration (AMD) patients. RESULTS: 6 months after surgery, several values were statistically significant in the group with higher RTA. Also patient compliance analysis (PCA) in relation to functional change perception appeared to be very good. METHODS: Thirty-six eyes of 25 patients (range 64-84 years of age) affected by dry AMD were included in study, and divided in two groups by spectral domain-optical coherence tomography (SD-OCT): group A with retinal thickness average (RTA) less than 250 microns (μm) and group B with RTA equal to or more than 250 μm. Adipocytes, adipose-derived stem cells from the stromal-vascular fraction, and platelets from platelet-rich plasma were implanted in the suprachoroidal space. Particularly, the following parameters were evaluated: best corrected visual acuity (BCVA) for far and near distance, retinal thickness maps, scotopic and photopic electroretinogram (ERG), and microperimetry (MY). All statistical analyses were performed with STATA 14.0 (Collage Station, Texas, USA). CONCLUSIONS: The available set of GFs allowed biological retinal neuroenhancement. After 6 months it improved visual performance (VP), but the increase was better if RTA recorded by OCT was higher, probably in relation to the presence of areas with greater cellularity.
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spelling pubmed-52169132017-01-17 Cell surgery and growth factors in dry age-related macular degeneration: visual prognosis and morphological study Limoli, Paolo Giuseppe Limoli, Celeste Vingolo, Enzo Maria Scalinci, Sergio Zaccaria Nebbioso, Marcella Oncotarget Research Paper: Gerotarget (Focus on Aging) BACKGROUND: The aim of this research was to study the overall restoration effect on residual retinal cells through surgically grafted autologous cells onto the surrounding tissue, choroid and retina in order to produce a constant secretion of growth factors (GFs) in dry age-related macular degeneration (AMD) patients. RESULTS: 6 months after surgery, several values were statistically significant in the group with higher RTA. Also patient compliance analysis (PCA) in relation to functional change perception appeared to be very good. METHODS: Thirty-six eyes of 25 patients (range 64-84 years of age) affected by dry AMD were included in study, and divided in two groups by spectral domain-optical coherence tomography (SD-OCT): group A with retinal thickness average (RTA) less than 250 microns (μm) and group B with RTA equal to or more than 250 μm. Adipocytes, adipose-derived stem cells from the stromal-vascular fraction, and platelets from platelet-rich plasma were implanted in the suprachoroidal space. Particularly, the following parameters were evaluated: best corrected visual acuity (BCVA) for far and near distance, retinal thickness maps, scotopic and photopic electroretinogram (ERG), and microperimetry (MY). All statistical analyses were performed with STATA 14.0 (Collage Station, Texas, USA). CONCLUSIONS: The available set of GFs allowed biological retinal neuroenhancement. After 6 months it improved visual performance (VP), but the increase was better if RTA recorded by OCT was higher, probably in relation to the presence of areas with greater cellularity. Impact Journals LLC 2016-07-06 /pmc/articles/PMC5216913/ /pubmed/27391437 http://dx.doi.org/10.18632/oncotarget.10442 Text en Copyright: © 2016 Limoli et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper: Gerotarget (Focus on Aging)
Limoli, Paolo Giuseppe
Limoli, Celeste
Vingolo, Enzo Maria
Scalinci, Sergio Zaccaria
Nebbioso, Marcella
Cell surgery and growth factors in dry age-related macular degeneration: visual prognosis and morphological study
title Cell surgery and growth factors in dry age-related macular degeneration: visual prognosis and morphological study
title_full Cell surgery and growth factors in dry age-related macular degeneration: visual prognosis and morphological study
title_fullStr Cell surgery and growth factors in dry age-related macular degeneration: visual prognosis and morphological study
title_full_unstemmed Cell surgery and growth factors in dry age-related macular degeneration: visual prognosis and morphological study
title_short Cell surgery and growth factors in dry age-related macular degeneration: visual prognosis and morphological study
title_sort cell surgery and growth factors in dry age-related macular degeneration: visual prognosis and morphological study
topic Research Paper: Gerotarget (Focus on Aging)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216913/
https://www.ncbi.nlm.nih.gov/pubmed/27391437
http://dx.doi.org/10.18632/oncotarget.10442
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