June 2015
Volume 56, Issue 7
Free
ARVO Annual Meeting Abstract  |   June 2015
Author Affiliations & Notes
  • Rina Yoza
    Kyoto University, Kyoto city, Japan
  • Tomoaki Murakami
    Kyoto University, Kyoto city, Japan
  • Akihito Uji
    Kyoto University, Kyoto city, Japan
  • Kiyoshi Suzuma
    Kyoto University, Kyoto city, Japan
  • Masahiro Fujimoto
    Kyoto University, Kyoto city, Japan
  • Shin Yoshitake
    Kyoto University, Kyoto city, Japan
  • Yoko Dodo
    Kyoto University, Kyoto city, Japan
  • RIMA GHASHUT
    Kyoto University, Kyoto city, Japan
  • Nagahisa Yoshimura
    Kyoto University, Kyoto city, Japan
  • Footnotes
    Commercial Relationships Rina Yoza, None; Tomoaki Murakami, None; Akihito Uji, None; Kiyoshi Suzuma, None; Masahiro Fujimoto, None; Shin Yoshitake, None; Yoko Dodo, None; RIMA GHASHUT, None; Nagahisa Yoshimura, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2015, Vol.56, 5961. doi:
Abstract

Purpose: It have been reported that ganglion cells are degenerated in diabetic retinopathy (DR), which is supported by the clinical data using fundus imaging to some extent. We herein investigated the findings in the nerve fiber layer (NFL) and ganglion cell layer (GCL) of DR on the en face images of swept-source optical coherence tomography (SS-OCT).

Methods: Fifty eyes from 34 patients with DR were included in this study (10 eyes with each grade of international DR severity scale). We obtained three-dimensional images in 6x6mm centering the fovea using SS-OCT (DRI OCT-1, TOPCON). After individual B-scan images were aligned by the ‘flattening’ function using the border between NFL and GCL, we observed en face images constructed by 256 B-scan images. We characterized the patchy lesions which had both lower reflectivity than the surrounding areas in NFL and higher reflectivity in GCL.

Results: The patchy lesions in NFL and GCL had the various shapes on en face OCT images, and their areas were 0.125±0.057 mm² at the level of NFL. Most lesions resided within NFL and GCL, and did not show any findings in the corresponding areas on color fundus photography. We further investigated the association between findings on fluorescein angiography (FA) and OCT in 23 eyes on whom both images were obtained. Mild hypofluorescence was accompanied with retinal capillaries in the areas corresponding to 78 patchy lesions on OCT images, and typical nonperfused areas were depicted in 8 lesions. Eyes with moderate nonproliferative diabetic retinopathy (NPDR), severe NPDR, and proliferative diabetic retinopathy were accompanied with the patchy lesions (the numbers in the individual grades were 4.4±3.7, 3.3±3.7, and 4.3±4.8, respectively), compared to no such lesions in eyes with no apparent retinopathy or mild NPDR.

Conclusions: We characterized a novel finding, the patchy lesion, at the levels of NFL and GCL on en face OCT images in DR, most of which did not correspond to any fundus findings but to mild hypofluorescence on FA images.

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