Investigative Ophthalmology & Visual Science Cover Image for Volume 65, Issue 7
June 2024
Volume 65, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2024
GAN-based High-definition 3-D Retinal Vasculature in Humans with Commercial OCT
Author Affiliations & Notes
  • Lingyun Wang
    Department of Ophthalmology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States
    Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania, United States
  • Bingjie Wang
    Department of Ophthalmology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States
  • Jay Chhablani
    Department of Ophthalmology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States
  • Jose Alain Sahel
    Department of Ophthalmology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States
  • Shaohua Pi
    Department of Ophthalmology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States
    Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania, United States
  • Footnotes
    Commercial Relationships   Lingyun Wang None; Bingjie Wang None; Jay Chhablani None; Jose Sahel None; Shaohua Pi None
  • Footnotes
    Support  We appreciate the funding from the Knight Templar Eye Foundation, Alcon Research Institute, and Eye & Ear Foundation of Pittsburgh to Dr. Shaohua Pi and Dr. Bingjie Wang. We also acknowledge support from NIH CORE Grant P30 EY08098, an unrestricted grant from Research to Prevent Blindness to the Department of Ophthalmology.
Investigative Ophthalmology & Visual Science June 2024, Vol.65, 3426. doi:
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    • Get Citation

      Lingyun Wang, Bingjie Wang, Jay Chhablani, Jose Alain Sahel, Shaohua Pi; GAN-based High-definition 3-D Retinal Vasculature in Humans with Commercial OCT. Invest. Ophthalmol. Vis. Sci. 2024;65(7):3426.

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

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Abstract

Purpose : To visualize 3-D organization of retinal vasculature in humans using single OCT/A scan.

Methods : OCT/A scans (3×3-mm, 400×400 A-lines) were collected using a PLEX® Elite 9000 swept-source OCT (ZEISS, Dublin, CA) at various retinal regions from healthy subjects. OCTA tail artifacts were removed by an advanced projection-removal algorithm. A ResNet-based generative adversarial network was designed to reconstruct the single scan OCTA volume, using merged (N=10) volumes as ground truth. For the training process, we proposed a percent retina projection strategy, i.e., to segment retinal layers and project multiple en face images at each percent depth slab, to ensure the network can better learn the retinal vasculature pattern. After training, the network was applied to reconstruct every depth plane to obtain the high-definition OCTA volume, requiring no layer segmentations. The reconstruction performance of the proposed strategy was compared to conventional depth plane and B-scan training schemes using the same network. Retinal arterioles and venules in OCTA images were correlated to the fundus image to investigate the organization of retinal vasculature.

Results : Thirty OCT/A scans from 10 subjects were included in this study. Five scans were used for training and the others were used for testing. Our proposed strategy achieved the best structural similarity index (SSIM) and learned perceptual image patch similarity (LPIPS) among three strategies by comparing the en face images of superficial capillary plexus (SCP), intermediate capillary plexus (ICP), and deep capillary plexus (DCP) (Fig. 1). From en face and volume visualization of the reconstructed OCTA volumes, we were able to confirm three features of retinal vasculature: 1) retinal arterioles typically have avascular zones and longer vascular bifurcation length; 2) capillary vortices frequently exist in DCP, especially at regions near fovea; and 3) retinal venules tend to extend to capillary vortices in DCP (Fig. 1 and 2).

Conclusions : The proposed deep learning reconstruction method enables detailed 3-D visualization of retinal vasculature using single OCT/A scan, which may pave a way to study their complex organization, pathogenesis and treatment response in various retino-vascular diseases.

This abstract was presented at the 2024 ARVO Annual Meeting, held in Seattle, WA, May 5-9, 2024.

 

 

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