Immunohistochemical, functional, and anatomical evaluation of patients with idiopathic epiretinal membrane

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Título: Immunohistochemical, functional, and anatomical evaluation of patients with idiopathic epiretinal membrane
Autor/es: Molina Martín, Julio César | Fernández Sánchez, Laura | Piñero, David P. | Cuenca, Nicolás
Grupo/s de investigación o GITE: Grupo de Óptica y Percepción Visual (GOPV) | Neurobiología del Sistema Visual y Terapia de Enfermedades Neurodegenerativas (NEUROVIS)
Centro, Departamento o Servicio: Universidad de Alicante. Departamento de Óptica, Farmacología y Anatomía | Universidad de Alicante. Departamento de Fisiología, Genética y Microbiología
Palabras clave: Epiretinal membrane | Pars plana vitrectomy | Müller cells | Astrocytes | Microglia | Macrophages | Spectraldomain optical coherence tomography | Immunohistochemical analysis
Fecha de publicación: 10-ene-2024
Editor: Springer Nature
Cita bibliográfica: Graefe's Archive for Clinical and Experimental Ophthalmology. 2024, 262: 1443-1453. https://doi.org/10.1007/s00417-023-06366-w
Resumen: Purpose The main purpose of this study was to perform an immunohistochemical, functional, and anatomical evaluation of patients with idiopathic epiretinal membrane (ERM). Methods Twenty-four specimens of idiopathic ERM from 24 consecutive patients who underwent 23 G pars plana vitrectomy for ERM and internal limiting membrane (ILM) peeling at the San Juan University Hospital in Alicante (Spain) in 2019 were analyzed. All patients underwent a complete ophthalmological examination including measurement of best corrected visual acuity (BCVA) and macular analysis by spectral-domain optical coherence tomography (SD-OCT) at the time of diagnosis and 3 months after surgery. Specific glial fibrillar acid protein antibodies (GFAP) and S100 calcium-binding protein β (S100β) immunostaining markers were used to identify the macroglial component of the ERM, Müller cells, and astrocytes. Ionized calcium-binding adapter molecule 1 protein (Iba1) antibodies were used as specific markers for inflammatory cells, such as microglia and macrophages. Results Mean preoperative BCVA measured with Snellen chart was 0.3 and 0.6 preoperatively and at 3 months after surgery, respectively. SD-OCT identified 15 patients (62.5%) with a disruption of the outer retinal hyperreflective bands. The immunohistochemical study showed the presence of Müller cells in almost all cases (91.6%), as well of abundant microglia and macrophages. Microglia and macrophages were more frequently present in earlier stages of ERM. Microglia were present in ERM independently of the outer retinal hyperreflective bands integrity as measured by SD-OCT. A greater presence of macrophages was found in those ERMs with no outer retinal hyperreflective band disruption. Conclusions Müller cells seem to be the most frequent cell group in ERMs, with also presence of microglia cells and macrophages. Astrocytes were more frequently found in early stages of ERMs. Microglia and macrophages were most frequent in ERMs with early stage (1, 2, or 3) than in advanced stages (4).
Patrocinador/es: Open Access funding provided thanks to the CRUE-CSIC agreement with Springer Nature.
URI: http://hdl.handle.net/10045/139644
ISSN: 0721-832X (Print) | 1435-702X (Online)
DOI: 10.1007/s00417-023-06366-w
Idioma: eng
Tipo: info:eu-repo/semantics/article
Derechos: © The Author(s) 2024. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
Revisión científica: si
Versión del editor: https://doi.org/10.1007/s00417-023-06366-w
Aparece en las colecciones:INV - NEUROVIS - Artículos de Revistas
INV - GOPV - Artículos de Revistas

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