基于融合OCTA扫描、人口统计学和临床生物标志物特征的3D多路径卷积神经网络的糖尿病视网膜病变分级

Nabila Eladawi, Mohammed M Elmogy, M. Ghazal, L. Fraiwan, A. Aboelfetouh, A. Riad, H. Sandhu, A. El-Baz
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引用次数: 2

摘要

糖尿病视网膜病变(DR)被认为是大多数国家劳动年龄人口视力丧失的主要原因之一。DR是由高血糖(糖尿病)引起的,这会损害视网膜血管并导致失明。DR的诊断和分级都需要对视网膜发生的变化进行人工测量和视觉评估,这是一项非常复杂的任务。因此,临床需要一种无创、客观的诊断系统,以提高DR早期体征和分级检测的准确性。本文提出了一种用于DR早期体征检测和分级的计算机辅助诊断(CAD)系统,从光学相干断层扫描血管造影(OCTA)扫描中提取出四个重要的视网膜血管特征,这些特征反映了DR进展过程中视网膜血管的变化。开发的系统将这四个重要特征与临床和人口统计学生物标志物融合在一起。该系统使用3D卷积神经网络(CNN)来分割OCTA深丛和浅丛的血管。最后,使用随机森林(RF)技术对这些提取的特征进行分类,首先区分DR和正常受试者。然后,将DR受试者分为轻度或中度。我们对一组患者(n == 100)进行DR分级的初步结果显示,平均准确率为96.8%,灵敏度为98.1%,特异性为88.8%。这些结果表明了该方法在早期检测和DR分级方面的可行性。
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Diabetic Retinopathy Grading Using 3D Multi-path Convolutional Neural Network Based on Fusing Features from OCTA Scans, Demographic, and Clinical Biomarkers
Diabetic Retinopathy (DR) is considered one of the major reasons for vision loss in the working-age population in most of the countries. DR is caused by high blood sugar levels (diabetes), which damages retinal blood vessels and leads to blindness. Both diagnosis and grading of DR require manual measurements and visual assessment of the changes that happen in the retina, which is a highly complex task. Thus, there is an unmet clinical need for a non-invasive and objective diagnostic system, which can improve the accuracy of both early signs and grading detection for DR. In this paper, we proposed a computer-aided diagnosis (CAD) system for detecting early signs as well as grading of DR. Four significant retinal vasculature features are extracted from optical coherence tomography angiography (OCTA) scans, which reflect the changes in the retinal blood vessels due to DR progress. The developed system fuses these four significant features with clinical and demographic biomarkers. The proposed system uses a 3D convolutional neural network (CNN) to segment blood vessels from both OCTA deep and superficial plexuses. Finally, these extracted features are classified by using the random forest (RF) technique to differentiate first between the DR from normal subjects. Then, grade the DR subjects into mild or moderate. Our preliminary results of grading DR in a cohort of patients (n == 100) demonstrated an average accuracy of 96.8%, sensitivity of 98.1%, and specificity of 88.8%. These results show the feasibility of the proposed approach in early detection as well as the grading of DR.
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