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Inner Macular Changes in Fellow Eye of Patients With Unilateral Idiopathic Epiretinal Membrane
PURPOSE: We evaluated a series of fellow eyes (FEs) in patients affected by unilateral idiopathic epiretinal membrane (IERM) with spectral-domain optical coherence tomography (SD-OCT) and OCT angiography (OCT-A) to determine if a previous defect in the inner retina is present before the mechanical d...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8399621/ https://www.ncbi.nlm.nih.gov/pubmed/34427622 http://dx.doi.org/10.1167/iovs.62.10.29 |
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author | Coppe, Andrea M. Lapucci, Giuliana Ripandelli, Guido Pesci, Francesca R. Buzzonetti, Luca Iarossi, Giancarlo |
author_facet | Coppe, Andrea M. Lapucci, Giuliana Ripandelli, Guido Pesci, Francesca R. Buzzonetti, Luca Iarossi, Giancarlo |
author_sort | Coppe, Andrea M. |
collection | PubMed |
description | PURPOSE: We evaluated a series of fellow eyes (FEs) in patients affected by unilateral idiopathic epiretinal membrane (IERM) with spectral-domain optical coherence tomography (SD-OCT) and OCT angiography (OCT-A) to determine if a previous defect in the inner retina is present before the mechanical damage to the inner limiting membrane (ILM) caused by posterior vitreous detachment. METHODS: In patients with IERM (N = 39), ganglion cell layer (GCL) thickness in FEs was assessed with SD-OCT; in a subgroup (N = 25) the vessel density (VD) at the superficial (SCP) and deep capillary plexus (DCP) was assessed with swept-source OCT-A (SS-OCT-A). These values were then compared with 30 age-matched healthy control eyes (CEs). The statistical analyses used SPSS software version 15.0 (SPSS, Inc., Chicago, IL, USA). Data collected underwent 1-way ANOVA. A level of P < 0.05 was accepted as statistically significant. RESULTS: The GCL thickness in the FEs was significantly lower than in CEs, with a significant thinning in all sectors except temporal ones (mean P < 0.001, superior P = 0.0002, superonasal P < 0.001, inferonasal P < 0.001, and inferior P = 0.002). The VD was significantly lower in the FEs in all sectors of SCP (mean P = 0.009, inner ring P = 0.028, and outer ring P = 0.007). CONCLUSIONS: GCL and SCP are significantly reduced in the FEs. These data suggest that a vascular defect in the SCP could cause a cellular loss in the inner retina that may determine the cascade events leading to the IERM proliferation; the diagnosis in a preclinical phase could provide a treatment strategy to prevent the progression of the disease. |
format | Online Article Text |
id | pubmed-8399621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Association for Research in Vision and Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-83996212021-09-13 Inner Macular Changes in Fellow Eye of Patients With Unilateral Idiopathic Epiretinal Membrane Coppe, Andrea M. Lapucci, Giuliana Ripandelli, Guido Pesci, Francesca R. Buzzonetti, Luca Iarossi, Giancarlo Invest Ophthalmol Vis Sci Retina PURPOSE: We evaluated a series of fellow eyes (FEs) in patients affected by unilateral idiopathic epiretinal membrane (IERM) with spectral-domain optical coherence tomography (SD-OCT) and OCT angiography (OCT-A) to determine if a previous defect in the inner retina is present before the mechanical damage to the inner limiting membrane (ILM) caused by posterior vitreous detachment. METHODS: In patients with IERM (N = 39), ganglion cell layer (GCL) thickness in FEs was assessed with SD-OCT; in a subgroup (N = 25) the vessel density (VD) at the superficial (SCP) and deep capillary plexus (DCP) was assessed with swept-source OCT-A (SS-OCT-A). These values were then compared with 30 age-matched healthy control eyes (CEs). The statistical analyses used SPSS software version 15.0 (SPSS, Inc., Chicago, IL, USA). Data collected underwent 1-way ANOVA. A level of P < 0.05 was accepted as statistically significant. RESULTS: The GCL thickness in the FEs was significantly lower than in CEs, with a significant thinning in all sectors except temporal ones (mean P < 0.001, superior P = 0.0002, superonasal P < 0.001, inferonasal P < 0.001, and inferior P = 0.002). The VD was significantly lower in the FEs in all sectors of SCP (mean P = 0.009, inner ring P = 0.028, and outer ring P = 0.007). CONCLUSIONS: GCL and SCP are significantly reduced in the FEs. These data suggest that a vascular defect in the SCP could cause a cellular loss in the inner retina that may determine the cascade events leading to the IERM proliferation; the diagnosis in a preclinical phase could provide a treatment strategy to prevent the progression of the disease. The Association for Research in Vision and Ophthalmology 2021-08-24 /pmc/articles/PMC8399621/ /pubmed/34427622 http://dx.doi.org/10.1167/iovs.62.10.29 Text en Copyright 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. |
spellingShingle | Retina Coppe, Andrea M. Lapucci, Giuliana Ripandelli, Guido Pesci, Francesca R. Buzzonetti, Luca Iarossi, Giancarlo Inner Macular Changes in Fellow Eye of Patients With Unilateral Idiopathic Epiretinal Membrane |
title | Inner Macular Changes in Fellow Eye of Patients With Unilateral Idiopathic Epiretinal Membrane |
title_full | Inner Macular Changes in Fellow Eye of Patients With Unilateral Idiopathic Epiretinal Membrane |
title_fullStr | Inner Macular Changes in Fellow Eye of Patients With Unilateral Idiopathic Epiretinal Membrane |
title_full_unstemmed | Inner Macular Changes in Fellow Eye of Patients With Unilateral Idiopathic Epiretinal Membrane |
title_short | Inner Macular Changes in Fellow Eye of Patients With Unilateral Idiopathic Epiretinal Membrane |
title_sort | inner macular changes in fellow eye of patients with unilateral idiopathic epiretinal membrane |
topic | Retina |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8399621/ https://www.ncbi.nlm.nih.gov/pubmed/34427622 http://dx.doi.org/10.1167/iovs.62.10.29 |
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