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Novel Detection and Restorative Levodopa Treatment for Preclinical Diabetic Retinopathy.
Motz, Cara T; Chesler, Kyle C; Allen, Rachael S; Bales, Katie L; Mees, Lukas M; Feola, Andrew J; Maa, April Y; Olson, Darin E; Thule, Peter M; Iuvone, P Michael; Hendrick, Andrew M; Pardue, Machelle T.
Afiliação
  • Motz CT; Center for Visual and Neurocognitive Rehabilitation, Atlanta Veterans Affairs Medical Center, Decatur, GA.
  • Chesler KC; Center for Visual and Neurocognitive Rehabilitation, Atlanta Veterans Affairs Medical Center, Decatur, GA.
  • Allen RS; Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA.
  • Bales KL; Center for Visual and Neurocognitive Rehabilitation, Atlanta Veterans Affairs Medical Center, Decatur, GA.
  • Mees LM; Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA.
  • Feola AJ; Center for Visual and Neurocognitive Rehabilitation, Atlanta Veterans Affairs Medical Center, Decatur, GA.
  • Maa AY; Department of Ophthalmology, Emory University, Atlanta, GA.
  • Olson DE; Center for Visual and Neurocognitive Rehabilitation, Atlanta Veterans Affairs Medical Center, Decatur, GA.
  • Thule PM; Center for Visual and Neurocognitive Rehabilitation, Atlanta Veterans Affairs Medical Center, Decatur, GA.
  • Iuvone PM; Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA.
  • Hendrick AM; Center for Visual and Neurocognitive Rehabilitation, Atlanta Veterans Affairs Medical Center, Decatur, GA.
  • Pardue MT; Department of Ophthalmology, Emory University, Atlanta, GA.
Diabetes ; 69(7): 1518-1527, 2020 07.
Article em En | MEDLINE | ID: mdl-32051147
ABSTRACT
Diabetic retinopathy (DR) is diagnosed clinically by directly viewing retinal vascular changes during ophthalmoscopy or through fundus photographs. However, electroretinography (ERG) studies in humans and rodents have revealed that retinal dysfunction is demonstrable prior to the development of visible vascular defects. Specifically, delays in dark-adapted ERG oscillatory potential (OP) implicit times in response to dim-flash stimuli (<-1.8 log cd · s/m2) occur prior to clinically recognized DR. Animal studies suggest that retinal dopamine deficiency underlies these early functional deficits. In this study, we randomized individuals with diabetes, without clinically detectable retinopathy, to treatment with either low- or high-dose Sinemet (levodopa plus carbidopa) for 2 weeks and compared their ERG findings with those of control subjects (no diabetes). We assessed dim-flash-stimulated OP delays using a novel handheld ERG system (RETeval) at baseline and 2 and 4 weeks. RETeval recordings identified significant OP implicit time delays in individuals with diabetes without retinopathy compared with age-matched control subjects (P < 0.001). After 2 weeks of Sinemet treatment, OP implicit times were restored to control values, and these improvements persisted even after a 2-week washout. We conclude that detection of dim-flash OP delays could provide early detection of DR and that Sinemet treatment may reverse retinal dysfunction.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carbidopa / Levodopa / Retinopatia Diabética / Eletrorretinografia Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Diabetes Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carbidopa / Levodopa / Retinopatia Diabética / Eletrorretinografia Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Diabetes Ano de publicação: 2020 Tipo de documento: Article