March 2012
Volume 53, Issue 14
Free
ARVO Annual Meeting Abstract  |   March 2012
Automated Segmentation of Retinal Layers in Macular OCT Images of Patients with Retinitis Pigmentosa
Author Affiliations & Notes
  • Qi Yang
    Topcon Adv Biomed Imaging Lab, Topcon Medical Systems, Oakland, New Jersey
  • Charles A. Reisman
    Topcon Adv Biomed Imaging Lab, Topcon Medical Systems, Oakland, New Jersey
  • Kinpui Chan
    Topcon Adv Biomed Imaging Lab, Topcon Medical Systems, Oakland, New Jersey
  • Rithambara Ramachandran
    Psychology,
    Columbia University, New York, New York
  • Ali S. Raza
    Psychology,
    Columbia University, New York, New York
  • Donald C. Hood
    Psychology,
    Ophthalmology,
    Columbia University, New York, New York
  • Footnotes
    Commercial Relationships  Qi Yang, Topcon Medical Systems, Inc (E); Charles A. Reisman, Topcon Medical Systems, Inc (E); Kinpui Chan, Topcon Medical Systems, Inc (E); Rithambara Ramachandran, None; Ali S. Raza, None; Donald C. Hood, Topcon Medical Systems, Inc (F, C)
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science March 2012, Vol.53, 4083. doi:
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    • Get Citation

      Qi Yang, Charles A. Reisman, Kinpui Chan, Rithambara Ramachandran, Ali S. Raza, Donald C. Hood; Automated Segmentation of Retinal Layers in Macular OCT Images of Patients with Retinitis Pigmentosa. Invest. Ophthalmol. Vis. Sci. 2012;53(14):4083.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : To provide an automated layer segmentation algorithm for quantifying structural changes of the outer segment and other retinal layers as seen on spectral domain optical coherence tomography scans of patients with retinitis pigmentosa (RP)[1].

Methods: : The current algorithm employs dual-gradient information to perform shortest path search [2,3]. Connected component analysis and heuristics have been added to improve the accuracy of intra-retinal boundary detection. The algorithm delineates the inner limiting membrane (ILM), the nerve fiber layer (NFL)/ganglion cells layer (GCL) border, the inner plexiform layer (IPL)/the inner nuclear layer (INL) border, INL/outer plexiform layer (OPL) border, and three other outer retinal boundaries in three-dimensional (3D) volume scans. To test the accuracy, the manually segmented border positions were compared to the automatic segmentation results of 88 B-scans acquired from 8 RP macular 3D scans (3D OCT-1000, Topcon Corp., Tokyo, Japan). To test the repeatability, the macular 3D scans of 13 eyes (each with two repetitions) were segmented and the intra-class correlation coefficients and the mean of standard deviations were calculated.

Results: : The absolute mean differences between the manual and automated border positions were less than or about two pixels: ILM 3.57±2.50µm, NFL/GCL 7.47±4.66µm, IPL/INL 6.19±2.26µm, INL/OPL 6.94±4.32µm, IS/OS 3.92±1.15µm, OS/retinal pigment epithelium 3.82±1.59µm, and Bruch’s membrane 4.63±2.26µm. The intra-class correlation coefficients for the seven boundaries ranged from 0.92 to 0.98. The standard deviations of segmented boundaries were between 2.64µm and 4.47µm.

Conclusions: : The automated RP segmentation algorithm demonstrated good accuracy and repeatability results for seven retinal boundaries. It provides a fast and objective approach to explore possible structural markers for RP progression.1. Hood DC, et al., Biomed Opt Express 2011. 2. Yang Q, et al., Opt Express 2010. 3. Yang Q, et al., Biomed Opt Express 2011.

Keywords: image processing • retina • retinal degenerations: hereditary 
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