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Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells In Vivo
Published on: September 22, 2017
Reproducibility of SD-OCT-based ganglion cell-layer thickness in glaucoma using two different segmentation
Mona K Garvin1, Kyungmoo Lee, Trudy L Burns
1Center for the Prevention and Treatment of Visual Loss, Iowa City VA Health Care System, Iowa City, Iowa.
Investigative Ophthalmology & Visual Science
|September 19, 2013
Summary
Spectral-domain optical coherence tomography (SD-OCT) measurements of the ganglion cell-inner plexiform layer (GCL+IPL) are highly reproducible in glaucoma patients. Both public and commercial algorithms demonstrate excellent reliability for GCL+IPL thickness assessment.
Area of Science:
- Ophthalmology
- Medical Imaging
- Glaucoma Research
Background:
- Glaucoma diagnosis and monitoring rely on detecting structural changes in the retina.
- Spectral-domain optical coherence tomography (SD-OCT) is a key imaging modality for assessing retinal nerve fiber layer and ganglion cell complex thickness.
- Accurate and reproducible measurements of the ganglion cell-layer-plus-inner plexiform-layer (GCL+IPL) are crucial for early glaucoma detection and management.
Purpose of the Study:
- To compare the reproducibility of GCL+IPL thickness measurements derived from SD-OCT using a publicly available (Iowa) algorithm versus a commercially available (Cirrus) algorithm.
- To evaluate the reliability of these algorithms in patients diagnosed with open-angle glaucoma or suspected glaucoma.
Main Methods:
- Prospective acquisition of macula SD-OCT volumes from both eyes of glaucoma patients on two separate visits within 4 months.
- Calculation of combined GCL+IPL thickness using two distinct algorithms: a graph-theoretical approach (Iowa) and Cirrus software's ganglion cell analysis module.
- Statistical analysis focused on intraclass correlation coefficients, intervisit standard deviations, and coefficients of variation to assess reproducibility.
Main Results:
- Both algorithms demonstrated high reproducibility, with intraclass correlation coefficients of 0.98 for the Iowa algorithm and 0.95 for the Cirrus algorithm.
- The Iowa algorithm showed lower intervisit standard deviations (1.55 μm) and coefficients of variation (2.2%) compared to the Cirrus algorithm (2.45 μm and 3.5%, respectively).
- P < 0.0001 indicated statistically significant differences in reproducibility metrics between the two algorithms.
Conclusions:
- SD-OCT-based GCL+IPL thickness measurements are highly reproducible in patients with early glaucoma.
- Both public and commercial algorithms provide reliable data for GCL+IPL assessment in glaucoma, with the Iowa algorithm exhibiting slightly superior reproducibility.

