4.6 Article

Identification and Characterization of Epivascular Glia Using En Face Optical Coherence Tomography

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AMERICAN JOURNAL OF OPHTHALMOLOGY
卷 229, 期 -, 页码 108-119

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.ajo.2021.03.014

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  1. Research to Prevent Blindness Inc (New York)

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This study aims to describe the clinical features of epivascular glia (EVG) using en face optical coherence tomography (OCT). The findings show that EVG is associated with older age, advanced posterior vitreous detachment (PVD), pseudophakia, and contractile epiretinal membrane (ERM). These lesions can be identified using en face OCT and support the role of Miller cell activation through ILM breaks triggered by PVD.
PURPOSE: The purpose of this study was to describe the clinical features of epivascular glia (EVG) using en face optical coherence tomography (OCT). DESIGN: Retrospective cross-sectional study. METHODS: Single-institution en face OCT images were reviewed. Eyes displaying EVG were captured with man-ual internal limiting membrane (ILM) segmentation and analyzed with customized segmentation . A random age-and sex-matched control group was selected to determine relative epiretinal membrane (ERM) prevalence. RESULTS: Characteristic hyper-reflective ILM plaques with dendrite-like radiations were identified using en face OCT and displayed vascular predilection. A total of 161 eyes with EVG (the EVG group) and 2,315 eyes with-out EVG (control group) were identified from a total co-hort of 1,298 patients (or 2,476 eyes). The prevalence of EVG was 161 of 2,476 eyes (6.5%) and 119 of 1,298 patients (9.2%) in the cohort. Mean age was 79.3 +/- 10.7 years old in the EVG group and 55.9 +/- 24.6 years old in the control group ( P < .001). An advanced posterior vitreous detachment (PVD) stage was more common in the EVG group (grade 3: 41.7%; grade 4: 48.6%) than in the control group (grade 3: 18.5%; grade 4: 26.9%; P < .001). Contractile ERM was present in 71 of 161 eyes (44.1%) with EVG compared to 30 of 161 eyes (18.6%) in a random age-and sex-matched control cohort without EVG ( P < .001). CONCLUSIONS: EVG previously described with histopathology and scanning electron microscopy can be identified using en face OCT. In this study, these lesions were associated with older age, pseudophakia, and advanced PVD, supporting the role of Miller cell activation through ILM breaks triggered by PVD, a pathogenic mechanism proposed by previous studies. Published by Elsevier Inc.

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