Nonperfused Retinal Capillaries -- A New Method Developed on OCT and OCTA

TL;DR

This study introduces a deep learning method to quantify nonperfused retinal capillaries using co-registered OCT and OCTA, revealing increased NPCs in AMD and DR and their correlation with disease features.

Contribution

A novel deep learning algorithm for segmenting and quantifying nonperfused retinal capillaries from OCT/OCTA images in AMD and DR patients.

Findings

NPCs are significantly increased in AMD and DR compared to controls.

The segmentation accuracy of the algorithm is 88.2%.

NPCs correlate with disease severity and specific retinal features.

Abstract

To develop a new method to quantify nonperfused retinal capillaries (NPCs) by using co-registered optical coherence tomography (OCT) and OCT angiography (OCTA), and to evaluate NPCs in eyes with age-related macular degeneration (AMD) and diabetic retinopathy (DR). Multiple consecutive 3x3-mm OCT/OCTA scans were obtained using a commercial device (Solix; Visionix/Optovue, Inc., California, USA). We averaged multiple registered OCT/OCTA scans to create high-definition volumes. The deep capillary plexus slab was defined and segmented. A novel deep learning denoising algorithm removed tissue background noise from capillaries in the en face OCT/OCTA. The algorithm segmented NPCs by identifying capillaries from OCT without corresponding flow signals in the OCTA. We then investigated the relationships between NPCs and known features in AMD and DR. The denoised en face OCT/OCTA revealed the structure and flow of the capillaries. The automatically segmented NPC achieved an accuracy of 88.2% compared to manual grading of DR. Compared to healthy controls, both the mean number and total length (mm) of NPCs were significantly increased in eyes with AMD and eyes with DR (P < 0.001). Compared to early and intermediate AMD, the number and total length of NPCs were significantly higher in advanced AMD (number: P<0.001, P<0.001; total length: P = 0.002, P =0.003). Geography atrophy, macular neovascularization, drusen volume, and extrafoveal avascular area (EAA) significantly correlated with increased NPCs (P<0.05). In eyes with DR, NPCs correlated with the number of microaneurysms and EAA (P<0.05). The presence of fluid did not significantly correlate with NPCs in AMD and DR. Conclusions A deep learning-based algorithm can segment and quantify retinal capillaries that lack flow using colocalized OCT/OCTA. This novel biomarker may be useful in AMD and DR.