Journal article
AxoNet 2.0: A Deep Learning-Based Tool for Morphometric Analysis of Retinal Ganglion Cell Axons
Translational vision science & technology, Vol.12(3), 9
03/01/2023
DOI: 10.1167/tvst.12.3.9
PMCID: PMC10020950
PMID: 36917117
Abstract
Assessment of glaucomatous damage in animal models is facilitated by rapid and accurate quantification of retinal ganglion cell (RGC) axonal loss and morphologic change. However, manual assessment is extremely time- and labor-intensive. Here, we developed AxoNet 2.0, an automated deep learning (DL) tool that (i) counts normal-appearing RGC axons and (ii) quantifies their morphometry from light micrographs.
A DL algorithm was trained to segment the axoplasm and myelin sheath of normal-appearing axons using manually-annotated rat optic nerve (ON) cross-sectional micrographs. Performance was quantified by various metrics (e.g., soft-Dice coefficient between predicted and ground-truth segmentations). We also quantified axon counts, axon density, and axon size distributions between hypertensive and control eyes and compared to literature reports.
AxoNet 2.0 performed very well when compared to manual annotations of rat ON (R2 = 0.92 for automated vs. manual counts, soft-Dice coefficient = 0.81 ± 0.02, mean absolute percentage error in axonal morphometric outcomes < 15%). AxoNet 2.0 also showed promise for generalization, performing well on other animal models (R2 = 0.97 between automated versus manual counts for mice and 0.98 for non-human primates). As expected, the algorithm detected decreased in axon density in hypertensive rat eyes (P ≪ 0.001) with preferential loss of large axons (P < 0.001).
AxoNet 2.0 provides a fast and nonsubjective tool to quantify both RGC axon counts and morphological features, thus assisting with assessing axonal damage in animal models of glaucomatous optic neuropathy.
This deep learning approach will increase rigor of basic science studies designed to investigate RGC axon protection and regeneration.
Details
- Title: Subtitle
- AxoNet 2.0: A Deep Learning-Based Tool for Morphometric Analysis of Retinal Ganglion Cell Axons
- Creators
- Vidisha Goyal - Georgia Institute of TechnologyA Thomas Read - The Wallace H. Coulter Department of Biomedical EngineeringMatthew D Ritch - The Wallace H. Coulter Department of Biomedical EngineeringBailey G Hannon - Georgia Institute of TechnologyGabriela Sanchez Rodriguez - The Wallace H. Coulter Department of Biomedical EngineeringDillon M Brown - The Wallace H. Coulter Department of Biomedical EngineeringAndrew J Feola - Emory UniversityAdam Hedberg-Buenz - University of IowaGrant A Cull - Legacy HealthJuan Reynaud - Legacy HealthMona K Garvin - University of IowaMichael G Anderson - University of IowaClaude F Burgoyne - Legacy HealthC Ross Ethier - The Wallace H. Coulter Department of Biomedical Engineering
- Resource Type
- Journal article
- Publication Details
- Translational vision science & technology, Vol.12(3), 9
- DOI
- 10.1167/tvst.12.3.9
- PMID
- 36917117
- PMCID
- PMC10020950
- NLM abbreviation
- Transl Vis Sci Technol
- ISSN
- 2164-2591
- eISSN
- 2164-2591
- Language
- English
- Date published
- 03/01/2023
- Academic Unit
- Electrical and Computer Engineering; Molecular Physiology and Biophysics; Ophthalmology and Visual Sciences
- Record Identifier
- 9984378333002771
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