Abstract

A methodology that applies hyperspectral imaging (HSI) on ophthalmoscope images to identify diabetic retinopathy (DR) stage is demonstrated. First, an algorithm for HSI image analysis is applied to the average reflectance spectra of simulated arteries and veins in ophthalmoscope images. Second, the average simulated spectra are categorized by using a principal component analysis (PCA) score plot. Third, Beer-Lambert law is applied to calculate vessel oxygen saturation in the ophthalmoscope images, and oxygenation maps are obtained. The average reflectance spectra and PCA results indicate that average reflectance changes with the deterioration of DR. The G-channel gradually decreases because of vascular disease, whereas the R-channel gradually increases with oxygen saturation in the vessels. As DR deteriorates, the oxygen utilization of retinal tissues gradually decreases, and thus oxygen saturation in the veins gradually increases. The sensitivity of diagnosis is based on the severity of retinopathy due to diabetes. Normal, background DR (BDR), pre-proliferative DR (PPDR), and proliferative DR (PDR) are arranged in order of 90.00%, 81.13%, 87.75%, and 93.75%, respectively; the accuracy is 90%, 86%, 86%, 90%, respectively. The F1-scores are 90% (Normal), 83.49% (BDR), 86.86% (PPDR), and 91.83% (PDR), and the accuracy rates are 95%, 91.5%, 93.5%, and 96%, respectively.

Highlights

  • A high circulating blood glucose is a major feature of diabetes, which can be divided into insulin-dependent diabetes mellitus and non-insulin-dependent diabetes mellitus [1,2]

  • The difference in reflectance spectrum shows a decreasing spectral reflectance according to the degree of lesion (Normal, background DR (BDR), pre-proliferative DR (PPDR), and proliferative DR (PDR))

  • In this study we use a relatively simple model to analyze the reflectance spectrum obtained by hyperspectral imaging (HSI), but it can be used as a basis for doctors to quickly diagnose diabetic retinopathy stage and pave the way for a more intricate model [39]

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Summary

Introduction

A high circulating blood glucose is a major feature of diabetes, which can be divided into insulin-dependent diabetes mellitus (type 1 diabetes) and non-insulin-dependent diabetes mellitus (type 2 diabetes) [1,2]. According to the IDF data in 2014, approximately four million people died from diabetic complications. Diabetic retinopathy (DR) is one of the major complications of microvascular injury. The condition may lead to vision loss [3]. The early clinical features of DR are microvascular and intraretinal hemorrhage [3,4]. Neovascularization initiates because microvessels are not perfused, and proliferative DR (PDR) is prone to retinal detachment if not treated in time and leads to vision loss [3]. 28 million people suffering from DR lose their sight. A total of 155 million people are expected to suffer from DR in 2030, and more than 51 million people may lose their sight [2]. The early detection and treatment of DR are crucial

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