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Enface Thickness Mapping and Reflectance Imaging of Retinal Layers in Diabetic Retinopathy.

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journal contribution
posted on 11.04.2016 by AW Francis, J Wanek, JI Lim, M Shahidi
PURPOSE: To present a method for image segmentation and generation of enface thickness maps and reflectance images of retinal layers in healthy and diabetic retinopathy (DR) subjects. METHODS: High density spectral domain optical coherence tomography (SDOCT) images were acquired in 10 healthy and 4 DR subjects. Customized image analysis software identified 5 retinal cell layer interfaces and generated thickness maps and reflectance images of the total retina (TR), inner retina (IR), outer retina (OR), and the inner segment ellipsoid (ISe) band. Thickness maps in DR subjects were compared to those of healthy subjects by generating deviation maps which displayed retinal locations with thickness below, within, and above the normal 95% confidence interval. RESULTS: In healthy subjects, TR and IR thickness maps displayed the foveal depression and increased thickness in the parafoveal region. OR and ISe thickness maps showed increased thickness at the fovea, consistent with normal retinal anatomy. In DR subjects, thickening and thinning in localized regions were demonstrated on TR, IR, OR, and ISe thickness maps, corresponding to retinal edema and atrophy, respectively. TR and OR reflectance images showed reduced reflectivity in regions of increased thickness. Hard exudates appeared as hyper-reflective spots in IR reflectance images and casted shadows on the deeper OR and ISe reflectance images. The ISe reflectance image clearly showed the presence of focal laser scars. CONCLUSIONS: Enface thickness mapping and reflectance imaging of retinal layers is a potentially useful method for quantifying the spatial and axial extent of pathologies due to DR.

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Funding

This work was supported by NIH research grants DK104393 and EY001792, Department of VA, Senior Scientific Investigator (MS) and unrestricted departmental awards from Research to Prevent Blindness

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Publisher Statement

This is a copy of an article published in the PLoS ONE © 2015 Public Library of Science Publications.

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PLoS One

issn

1932-6203

Issue date

23/12/2015

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