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Cystic Fibrosis and New Trends by Ophthalmological Evaluation: A Pilot Study
Background. Cystic fibrosis (CF) is characterized by hypoxia that affects several organic tissues. Retinal ganglion cells may suffer from the hypoxic status, and this may lead to alterations of retinal nerve fiber. Methods. Twenty-two eyes in CF patients were analyzed. A complete ocular evaluation a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4123475/ https://www.ncbi.nlm.nih.gov/pubmed/25133169 http://dx.doi.org/10.1155/2014/580373 |
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author | Nebbioso, Marcella Quattrucci, Serena Leggieri, Emanuela Spadea, Leopoldo Vingolo, Enzo Maria |
author_facet | Nebbioso, Marcella Quattrucci, Serena Leggieri, Emanuela Spadea, Leopoldo Vingolo, Enzo Maria |
author_sort | Nebbioso, Marcella |
collection | PubMed |
description | Background. Cystic fibrosis (CF) is characterized by hypoxia that affects several organic tissues. Retinal ganglion cells may suffer from the hypoxic status, and this may lead to alterations of retinal nerve fiber. Methods. Twenty-two eyes in CF patients were analyzed. A complete ocular evaluation and visual field exams of the 30 central degrees were performed using the frequency doubling technology (FDT). Forced expiratory volume in one second (FEV1%), forced vital capacity (FVC%), oxyhaemoglobin saturation (SpO(2)%), and hematocrit (Ht%) have been calculated. FDT analyzed parameters were mean deviation (MD) and pattern standard deviation (PSD). Pearson's correlation was chosen as statistical analysis. Results. Data showed statistically significant relationship between MD and Ht% (r value −0.18; P = 0.04), MD and FEV1% (r value −0.68; P = 0.001), and MD and FVC% (r value −0.45; P = 0.005). Moreover, there were correlations between PSD and Ht% (r value 0.29; P = 0.03), PSD and SpO(2)% (r value −0.31; P = 0.01), PSD and FEV1% (r value 0.71; P = 0.0005), and PSD and FVC% (r value 0.63; P = 0.003). Conclusions. The oxygen supply alterations might determine hypoxia of the ganglion cells causing a decrease of receptive optic nerve fiber activity. This method could be also useful to evaluate indirectly pulmonary activity of the CF disease. |
format | Online Article Text |
id | pubmed-4123475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-41234752014-08-17 Cystic Fibrosis and New Trends by Ophthalmological Evaluation: A Pilot Study Nebbioso, Marcella Quattrucci, Serena Leggieri, Emanuela Spadea, Leopoldo Vingolo, Enzo Maria Biomed Res Int Research Article Background. Cystic fibrosis (CF) is characterized by hypoxia that affects several organic tissues. Retinal ganglion cells may suffer from the hypoxic status, and this may lead to alterations of retinal nerve fiber. Methods. Twenty-two eyes in CF patients were analyzed. A complete ocular evaluation and visual field exams of the 30 central degrees were performed using the frequency doubling technology (FDT). Forced expiratory volume in one second (FEV1%), forced vital capacity (FVC%), oxyhaemoglobin saturation (SpO(2)%), and hematocrit (Ht%) have been calculated. FDT analyzed parameters were mean deviation (MD) and pattern standard deviation (PSD). Pearson's correlation was chosen as statistical analysis. Results. Data showed statistically significant relationship between MD and Ht% (r value −0.18; P = 0.04), MD and FEV1% (r value −0.68; P = 0.001), and MD and FVC% (r value −0.45; P = 0.005). Moreover, there were correlations between PSD and Ht% (r value 0.29; P = 0.03), PSD and SpO(2)% (r value −0.31; P = 0.01), PSD and FEV1% (r value 0.71; P = 0.0005), and PSD and FVC% (r value 0.63; P = 0.003). Conclusions. The oxygen supply alterations might determine hypoxia of the ganglion cells causing a decrease of receptive optic nerve fiber activity. This method could be also useful to evaluate indirectly pulmonary activity of the CF disease. Hindawi Publishing Corporation 2014 2014-07-15 /pmc/articles/PMC4123475/ /pubmed/25133169 http://dx.doi.org/10.1155/2014/580373 Text en Copyright © 2014 Marcella Nebbioso et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Nebbioso, Marcella Quattrucci, Serena Leggieri, Emanuela Spadea, Leopoldo Vingolo, Enzo Maria Cystic Fibrosis and New Trends by Ophthalmological Evaluation: A Pilot Study |
title | Cystic Fibrosis and New Trends by Ophthalmological Evaluation: A Pilot Study |
title_full | Cystic Fibrosis and New Trends by Ophthalmological Evaluation: A Pilot Study |
title_fullStr | Cystic Fibrosis and New Trends by Ophthalmological Evaluation: A Pilot Study |
title_full_unstemmed | Cystic Fibrosis and New Trends by Ophthalmological Evaluation: A Pilot Study |
title_short | Cystic Fibrosis and New Trends by Ophthalmological Evaluation: A Pilot Study |
title_sort | cystic fibrosis and new trends by ophthalmological evaluation: a pilot study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4123475/ https://www.ncbi.nlm.nih.gov/pubmed/25133169 http://dx.doi.org/10.1155/2014/580373 |
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