Title:
How to Improve Detection and Treatment of Diabetic Retinopathy

dc.contributor.author Pardue, Machelle T.
dc.contributor.corporatename Georgia Institute of Technology. Neural Engineering Center en_US
dc.contributor.corporatename Georgia Institute of Technology. Wallace H. Coulter Dept. of Biomedical Engineering en_US
dc.date.accessioned 2017-04-10T17:08:47Z
dc.date.available 2017-04-10T17:08:47Z
dc.date.issued 2017-03-27
dc.description Presented on March 27, 2017 at 11:00 a.m. in the Engineered Biosystems Building (EBB), room 1005. en_US
dc.description Machelle Pardue is a professor in the Wallace H. Coulter Department of Biomedical Engineering at Georgia Tech and Emory University. Her research interestss are neuroprotective treatments, retinal mechanisms of refractive development, diabetic retinopathy. en_US
dc.description Runtime: 53:29 minutes en_US
dc.description.abstract Diabetic retinopathy (DR) is the leading cause of blindness in working age adults. DR is clinically diagnosed by late stage vascular changes in the retina. Detecting early stage retinopathy prior to the onset of these clinical findings would greatly impact the management and treatment of DR. We have identified several tests that show dysfunction in the retina prior to the onset of vascular lesions induced by diabetes. Using novel stimuli with the electroretinogram, we have determined that rod photoreceptor function is most vulnerable to diabetes. Our studies show similar delays in rodent models of diabetes and diabetic patients, prior to clinically diagnosed DR, suggesting a potential screening tool. In addition, we have shown that spatial frequency and contrast sensitivity thresholds decline prior to vascular changes when tested with moving gratings. Finally, we have demonstrated the application of reactive fluorescent tags to detect reactive oxygen species in the retina, providing another possible screening tool for DR. The detection of early stage DR opens a therapeutic window for neuroprotective agents that could slow or halt the progression of disease. We have demonstrated that L-DOPA or exercise treatments are promising interventions to slow the progression of DR and preserve visual function. en_US
dc.format.extent 53:29 minutes
dc.identifier.uri http://hdl.handle.net/1853/56626
dc.language.iso en_US en_US
dc.relation.ispartofseries GT Neuro Seminar Series
dc.subject Diabetic retinopathy en_US
dc.subject Dopamine en_US
dc.subject Exercise en_US
dc.title How to Improve Detection and Treatment of Diabetic Retinopathy en_US
dc.type Moving Image
dc.type.genre Lecture
dspace.entity.type Publication
local.contributor.author Pardue, Machelle T.
local.contributor.corporatename Neural Engineering Center
local.relation.ispartofseries GT Neuro Seminar Series
relation.isAuthorOfPublication c0521c82-367a-4016-94d3-b5a1afd859c7
relation.isOrgUnitOfPublication c2e26044-257b-4ef6-8634-100dd836a06c
relation.isSeriesOfPublication 608bde12-7f29-495f-be22-ac0b124e68c5
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