Microcystic Macular Edema Caused by Non-Glaucomatous Optic Atrophy: A Single-Center, Retrospective, Cohort Study in France

Author:

Coutureau Tibaut1,Butterworth Jacqueline1,Biotti Damien23ORCID,Fournié Pierre14ORCID,Soler Vincent14,Varenne Fanny1ORCID

Affiliation:

1. Ophthalmology Department, Pierre-Paul Riquet Hospital, Toulouse University Hospital, 31059 Toulouse, France

2. Department of Neurology, Toulouse University Hospital, 31059 Toulouse, France

3. Toulouse Institute for Infectious and Inflammatory Diseases, INSERM U1043, CNRS UMR 5282, 31024 Toulouse, France

4. Faculty of Medicine, University of Toulouse III, 31400 Toulouse, France

Abstract

Optic Atrophy (OA) can be associated with the development of microcystic macular edema (MME) in the perifoveal retinal inner nuclear layer (INL). We aimed here to retrospectively determine the prevalence of MME in patients with non-glaucomatous OA in our tertiary ophthalmology department between 2015 and 2020. We then examined how MME affected the thicknesses of the different retinal layers and the differences in demographic and clinical characteristics between those patients who developed MME and those who did not. A total of 643 eyes (429 patients) were included (mean age 45.9 ± 17.8 years, 52% female). MME developed in 95 (15%) eyes and across all etiologies of OA except for toxic/nutritional causes, but the prevalence of MME varied between the different etiologies. The development of MME was associated with thinning of the ganglion cell layer (11.0 vs. 9.6 μm; p = 0.001) and the retinal nerve fiber layer (10.1 vs. 9.15 μm; p = 0.024), with INL thickening in the 3- and 6-mm diameter areas of the central fovea. Patients developing MME had significantly worse distance best-corrected visual acuity than those not developing MME (0.62 vs. 0.38 logMAR; p = 0.002). Overall, the presence of MME in OA cannot be used to guide the diagnostic work-up of OA.

Publisher

MDPI AG

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