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Author Spotlight: Ex Vivo OCT-Based Multimodal Imaging of Human Donor Eyes for Research into Age-Related Macular Degeneration
Published on: May 26, 2023
Microcystic macular edema: retrograde maculopathy caused by optic neuropathy
Mathias Abegg1, Muriel Dysli1, Sebastian Wolf1
1Department of Ophthalmology, Inselspital, Bern University Hospital, and University of Bern, Bern, Switzerland.
Purpose:
To investigate retrograde axonal degeneration for its potential to cause microcystic macular edema (MME), a maculopathy that has been previously described in patients with demyelinating disease. To identify risk factors for MME and to expand the anatomic knowledge on MME.
Design:
Retrospective case series.
Participants:
We included 117 consecutive patients and 180 eyes with confirmed optic neuropathy of variable etiology. Patients with glaucoma were excluded.
Methods:
We determined age, sex, visual acuity, etiology of optic neuropathy, and the temporal and spatial characteristics of MME. Eyes with MME were compared with eyes with optic neuropathy alone and to healthy fellow eyes. With retinal layer segmentation we quantitatively measured the intraretinal anatomy.
Main Outcome Measures:
Demographic data, distribution of MME in the retina, and thickness of retinal layers were analyzed.
Results:
We found MME in 16 eyes (8.8%) from 9 patients, none of whom had multiple sclerosis or neuromyelitis optica. The MME was restricted to the inner nuclear layer (INL) and had a characteristic perifoveal circular distribution. Compared with healthy controls, MME was associated with significant thinning of the ganglion cell layer and nerve fiber layer, as well as a thickening of the INL and the deeper retinal layers. Youth is a significant risk factor for MME.
Conclusions:
Microcystic macular edema is not specific for demyelinating disease. It is a sign of optic neuropathy irrespective of its etiology. The distinctive intraretinal anatomy suggests that MME is caused by retrograde degeneration of the inner retinal layers, resulting in impaired fluid resorption in the macula.
Insights
Microcystic macular edema (MME) is a sign of optic neuropathy, not just demyelinating disease. This study found MME is linked to retrograde degeneration in retinal layers, with youth being a risk factor.
Area of Science:
- Ophthalmology
- Neuroscience
- Retinal Imaging
Background:
- Microcystic macular edema (MME) has been observed in demyelinating diseases.
- The underlying pathophysiology and risk factors for MME require further elucidation.
Purpose of the Study:
- To investigate retrograde axonal degeneration as a cause of MME.
- To identify risk factors associated with MME.
- To expand the anatomical understanding of MME.
Main Methods:
- Retrospective case series of 117 patients (180 eyes) with optic neuropathy (excluding glaucoma).
- Analysis of demographic data, visual acuity, and etiology of optic neuropathy.
- Quantitative measurement of intraretinal anatomy using retinal layer segmentation.
Main Results:
- MME was present in 8.8% of eyes, primarily in the inner nuclear layer with a perifoveal distribution.
- MME correlated with thinning of ganglion cell and nerve fiber layers, and thickening of the inner nuclear and deeper retinal layers.
- Younger age was identified as a significant risk factor for MME.
Conclusions:
- MME is not exclusive to demyelinating diseases and indicates optic neuropathy regardless of cause.
- The observed intraretinal changes suggest MME results from retrograde degeneration and impaired fluid resorption.
- MME provides insights into the structural consequences of optic neuropathy.
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