scholarly journals Development and Validation of a Deep Learning System for Diabetic Retinopathy and Related Eye Diseases Using Retinal Images From Multiethnic Populations With Diabetes

JAMA ◽  
2017 ◽  
Vol 318 (22) ◽  
pp. 2211 ◽  
Author(s):  
Daniel Shu Wei Ting ◽  
Carol Yim-Lui Cheung ◽  
Gilbert Lim ◽  
Gavin Siew Wei Tan ◽  
Nguyen D. Quang ◽  
...  
2020 ◽  
Vol 26 (4) ◽  
pp. 429-443 ◽  
Author(s):  
Lijun Zhao ◽  
Honghong Ren ◽  
Junlin Zhang ◽  
Yana Cao ◽  
Yiting Wang ◽  
...  

Objective: To characterize the relationship between diabetic retinopathy (DR) and diabetic nephropathy (DN) in Chinese patients and to determine whether the severity of DR predicts end-stage renal disease (ESRD). Methods: Bilateral fundic photographs of 91 Chinese type 2 diabetic patients with biopsy-confirmed DN, not in ESRD stage, were obtained at the time of renal biopsy in this longitudinal study. The baseline severity of DR was determined using the Lesion-aware Deep Learning System (RetinalNET) in an open framework for deep learning and was graded using the Early Treatment Diabetic Retinopathy Study severity scale. Cox proportional hazard models were used to estimate the hazard ratio (HR) for the effect of the severity of diabetic retinopathy on ESRD. Results: During a median follow-up of 15 months, 25 patients progressed to ESRD. The severity of retinopathy at the time of biopsy was a prognostic factor for progression to ESRD (HR 2.18, 95% confidence interval 1.05 to 4.53, P = .04). At baseline, more severe retinopathy was associated with poor renal function, and more severe glomerular lesions. However, 30% of patients with mild retinopathy and severe glomerular lesions had higher low-density lipo-protein-cholesterol and more severe proteinuria than those with mild glomerular lesions. Additionally, 3% of patients with severe retinopathy and mild glomerular changes were more likely to have had diabetes a long time than those with severe glomerular lesions. Conclusion: Although the severity of DR predicted diabetic ESRD in patients with type 2 diabetes mellitus and DN, the severities of DR and DN were not always consistent, especially in patients with mild retinopathy or microalbuminuria. Abbreviations: CI = confidence interval; DM = diabetic mellitus; DN = diabetic nephropathy; DR = diabetic retinopathy; eGFR = estimated glomerular filtration rate; ESRD = end-stage renal disease; HbA1c = hemoglobin A1c; HR = hazard ratio; NPDR = nonproliferative diabetic retinopathy; PDR = proliferative diabetic retinopathy; SBP = systolic blood pressure; T2DM = type 2 diabetes mellitus; VEGF = vascular endothelial growth factor


2019 ◽  
Vol 8 (2S11) ◽  
pp. 3637-3640

Retinal vessels ID means to isolate the distinctive retinal configuration issues, either wide or restricted from fundus picture foundation, for example, optic circle, macula, and unusual sores. Retinal vessels recognizable proof investigations are drawing in increasingly more consideration today because of pivotal data contained in structure which is helpful for the identification and analysis of an assortment of retinal pathologies included yet not restricted to: Diabetic Retinopathy (DR), glaucoma, hypertension, and Age-related Macular Degeneration (AMD). With the advancement of right around two decades, the inventive methodologies applying PC supported systems for portioning retinal vessels winding up increasingly significant and coming nearer. Various kinds of retinal vessels segmentation strategies discussed by using Deep Learning methods. At that point, the pre-processing activities and the best in class strategies for retinal vessels distinguishing proof are presented.


Author(s):  
Zhan Wei Lim ◽  
Mong Li Lee ◽  
Wynne Hsu ◽  
Tien Yin Wong

Though deep learning systems have achieved high accuracy in detecting diseases from medical images, few such systems have been deployed in highly automated disease screening settings due to lack of trust in how well these systems can generalize to out-of-datasets. We propose to use uncertainty estimates of the deep learning system’s prediction to know when to accept or to disregard its prediction. We evaluate the effectiveness of using such estimates in a real-life application for the screening of diabetic retinopathy. We also generate visual explanation of the deep learning system to convey the pixels in the image that influences its decision. Together, these reveal the deep learning system’s competency and limits to the human, and in turn the human can know when to trust the deep learning system.


Author(s):  
Vani Ashok ◽  
◽  
Navneet Hosmane ◽  
Ganesh Mahagaonkar ◽  
Aditya Gudigar ◽  
...  

Diabetic Retinopathy (DR) is one of the serious problems caused by diabetes and a leading source of blindness in the working-age population of the advanced world. Detecting DR in the early stages is crucial since the disease generally shows few symptoms until it is too late to provide an effective cure. But detecting DR requires a skilled clinician to examine and assess digital color fundus images of the retina. By simplifying the detection process, severe damages to the eyes can be prevented. Many deep learning models particularly Convolutional Neural Networks (CNNs) have been tested in similar fields as well as in the detection of DR in early stages. In this paper, we propose an automatic model for detecting and suggesting different stages of DR. The work has been carried out on APTOS 2019 Blindness Detection Benchmark Dataset which contains around 3600 retinal images graded by clinicians for the severity of diabetic retinopathy on a range of 0 to 4. The proposed method uses ResNet50 (Residual Network that is 50 layers deep) CNN model along with pre-trained weights as the base neural network model. Due to its depth and better transfer learning capabilities, the proposed model with ResNet50 achieved 82% classification accuracy. The classification ability of the model was further analysed with Cohen Kappa score. The optimized validation Cohen Kappa score of 0.827 indicate that the proposed model didn’t predict the outputs by chance.


2019 ◽  
Vol 98 (4) ◽  
pp. 368-377 ◽  
Author(s):  
Cristina González‐Gonzalo ◽  
Verónica Sánchez‐Gutiérrez ◽  
Paula Hernández‐Martínez ◽  
Inés Contreras ◽  
Yara T. Lechanteur ◽  
...  

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