2011
DOI: 10.1166/jmihi.2011.1015
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Study of Retinal Biometric Systems with Respect to Feature Classification for Recognition and Diabetic Retinopathy

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Cited by 6 publications
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“…High-dose STZ-induced type 1 diabetic rats, low-dose STZ-induced combined with high-fat diet-induced type 2 diabetic rats, and spontaneous type 2 diabetic KKAy mice are some of the most common models used to study diabetes and its complications. These models are modeled by destroying pancreatic tissue or increasing the fat intake, resulting in a complete or relative deficiency in insulin secretion, leading to abnormal blood glucose and/or insulin resistance, which causes intracellular mitochondrial damage ( 14 ), abnormal vascular endothelial cell function, excessive inflammation and oxidative stress, and other pathological processes ( 8 , 15 ), ultimately leading to a disruption of the blood-retinal barrier and retinal vascular leakage ( 16 , 17 ), by which point the lesion has shifted from the neuronal cells to the vascular endothelium and pericytes. From this perspective, the conventional diabetic animal model is not a model of retinal neurodegenerative disease and the use of a conventional diabetic animal model is more suitable for evaluating the efficacy of drugs to improve vasculopathy than for evaluating the efficacy of drugs to delay retinal nerve cell degeneration.…”
Section: Discussionmentioning
confidence: 99%
“…High-dose STZ-induced type 1 diabetic rats, low-dose STZ-induced combined with high-fat diet-induced type 2 diabetic rats, and spontaneous type 2 diabetic KKAy mice are some of the most common models used to study diabetes and its complications. These models are modeled by destroying pancreatic tissue or increasing the fat intake, resulting in a complete or relative deficiency in insulin secretion, leading to abnormal blood glucose and/or insulin resistance, which causes intracellular mitochondrial damage ( 14 ), abnormal vascular endothelial cell function, excessive inflammation and oxidative stress, and other pathological processes ( 8 , 15 ), ultimately leading to a disruption of the blood-retinal barrier and retinal vascular leakage ( 16 , 17 ), by which point the lesion has shifted from the neuronal cells to the vascular endothelium and pericytes. From this perspective, the conventional diabetic animal model is not a model of retinal neurodegenerative disease and the use of a conventional diabetic animal model is more suitable for evaluating the efficacy of drugs to improve vasculopathy than for evaluating the efficacy of drugs to delay retinal nerve cell degeneration.…”
Section: Discussionmentioning
confidence: 99%
“…Type 2 diabetes mellitus is associated with cardiovascular diseases [3], neuropathy [4], peripheral vascular insufficiency [5], lung dysfunction [6], and retinopathy [7].…”
Section: Introductionmentioning
confidence: 99%