June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
Automated segmentation of the in-vivo lamina cribrosa (LC) imaged using 3D optical coherence tomography (OCT)
Author Affiliations & Notes
  • Bo Wang
    UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Department of Ophthalmology, University of Pittsburgh, Pittsburgh, PA
    Medical Scientist Training Program, University of Pittsburgh, Pittsburgh, PA
  • Zach Nadler
    UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Department of Ophthalmology, University of Pittsburgh, Pittsburgh, PA
  • Jessica Nevins
    UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Department of Ophthalmology, University of Pittsburgh, Pittsburgh, PA
  • Richard Bilonick
    UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Department of Ophthalmology, University of Pittsburgh, Pittsburgh, PA
    Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA
  • Hiroshi Ishikawa
    UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Department of Ophthalmology, University of Pittsburgh, Pittsburgh, PA
    Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA
  • Larry Kagemann
    UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Department of Ophthalmology, University of Pittsburgh, Pittsburgh, PA
    Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA
  • Ireneusz Grulkowski
    Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, MA
  • Jonathan Liu
    Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, MA
  • James Fujimoto
    Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, MA
  • Joel Schuman
    UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Department of Ophthalmology, University of Pittsburgh, Pittsburgh, PA
    Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA
  • Footnotes
    Commercial Relationships Bo Wang, None; Zach Nadler, None; Jessica Nevins, None; Richard Bilonick, None; Hiroshi Ishikawa, None; Larry Kagemann, None; Ireneusz Grulkowski, None; Jonathan Liu, None; James Fujimoto, Carl Zeiss Meditec (P), Optovue (P), Optovue (I); Joel Schuman, Carl Zeiss Meditec, Inc. (P)
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 5499. doi:
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      Bo Wang, Zach Nadler, Jessica Nevins, Richard Bilonick, Hiroshi Ishikawa, Larry Kagemann, Ireneusz Grulkowski, Jonathan Liu, James Fujimoto, Joel Schuman; Automated segmentation of the in-vivo lamina cribrosa (LC) imaged using 3D optical coherence tomography (OCT). Invest. Ophthalmol. Vis. Sci. 2013;54(15):5499.

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

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Abstract
 
Purpose
 

The LC plays an important role in the pathogenesis of glaucoma, yet little work had been done to characterize its microstructures in-vivo. 3D analysis of the LC using manual segmentation is prohibitive due to the extended time required. We aimed to investigate an automated segmentation method for the in-vivo LC imaged using swept-source OCT (SS-OCT).

 
Methods
 

15 subjects (4 healthy, 5 glaucoma suspects, 6 glaucoma) were scanned using a prototype SS-OCT in a 3.5 x 3.5 x 3.64 mm area (400 x 400 x 896 pixels) of the optic nerve head. The region outside the LC was masked and the stack of C-mode slices underwent a median filter, local contrast enhancement and thresholding (Figure). A randomly selected C-mode scan for each subject was independently manually segmented using FIJI by 2 users and compared with the automated method for: (1) segmentation time, (2) sensitivity and specificity assuming pores marked by manual segmentations as the gold standard, (3) pore count, (4) pore area, (5) pore aspect ratio and (6) pore circularity. The measurements (3-6) were compared by computing bias and imprecision using a measurement error model. The automated segmentation and analysis was completed on 8 healthy eyes (Table).

 
Results
 

Average segmentation time was significantly faster using automated segmentation. Average sensitivity and specificity of the automated segmentation for detecting pores was 90.9±9.4% and 87.4±3.3%, respectively. There was no statistically significant difference in bias and imprecision between manual and automated segmentation for all investigated parameters though wide confidence interval were noted for all.

 
Conclusions
 

We herein propose a segmentation algorithm that provides an efficient segmentation of the LC with high sensitivity and specificity and with no statistically significant difference in bias and imprecision from manual segmentation. Wide confidence intervals indicate the inherent difficulty in segmenting the LC. 3D automated segmentation results of healthy LC are consistent with literature values for available parameters.

 
 
Table: LC parameters for healthy eyes.
 
Table: LC parameters for healthy eyes.
 
 
Figure: (A) Stacks of cross-sectional images are resampled into (B) C-mode slices (dotted lines on A). (C) Pore (green) and beam (red) segmentations. (D) Overlay of manual (red) and automated (green) segmentation. 3D rendering of the segmented LC beams from the (E) anterior and (F) posterior directions.
 
Figure: (A) Stacks of cross-sectional images are resampled into (B) C-mode slices (dotted lines on A). (C) Pore (green) and beam (red) segmentations. (D) Overlay of manual (red) and automated (green) segmentation. 3D rendering of the segmented LC beams from the (E) anterior and (F) posterior directions.
 
Keywords: 550 imaging/image analysis: clinical • 627 optic disc  
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