Your browser doesn't support javascript.
loading
In Vivo Multimodal Imaging of Drusenoid Lesions in Rhesus Macaques.
Yiu, Glenn; Tieu, Eric; Munevar, Christian; Wong, Brittany; Cunefare, David; Farsiu, Sina; Garzel, Laura; Roberts, Jeffrey; Thomasy, Sara M.
Afiliação
  • Yiu G; Department of Ophthalmology & Vision Science, University of California, Davis, Sacramento, California, USA. gyiu@ucdavis.edu.
  • Tieu E; Department of Ophthalmology & Vision Science, University of California, Davis, Sacramento, California, USA.
  • Munevar C; Department of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California, Davis, Davis, California, USA.
  • Wong B; Department of Biomedical Engineering, Duke University, Durham, North Carolina, USA.
  • Cunefare D; Department of Biomedical Engineering, Duke University, Durham, North Carolina, USA.
  • Farsiu S; Department of Biomedical Engineering, Duke University, Durham, North Carolina, USA.
  • Garzel L; California National Primate Research Center, Davis, California, USA.
  • Roberts J; Department of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California, Davis, Davis, California, USA.
  • Thomasy SM; California National Primate Research Center, Davis, California, USA.
Sci Rep ; 7(1): 15013, 2017 11 03.
Article em En | MEDLINE | ID: mdl-29101353
ABSTRACT
Nonhuman primates are the only mammals to possess a true macula similar to humans, and spontaneously develop drusenoid lesions which are hallmarks of age-related macular degeneration (AMD). Prior studies demonstrated similarities between human and nonhuman primate drusen based on clinical appearance and histopathology. Here, we employed fundus photography, spectral domain optical coherence tomography (SD-OCT), fundus autofluorescence (FAF), and infrared reflectance (IR) to characterize drusenoid lesions in aged rhesus macaques. Of 65 animals evaluated, we identified lesions in 20 animals (30.7%). Using the Age-Related Eye Disease Study 2 (AREDS2) grading system and multimodal imaging, we identified two distinct drusen phenotypes - 1) soft drusen that are larger and appear as hyperreflective deposits between the retinal pigment epithelium (RPE) and Bruch's membrane on SD-OCT, and 2) hard, punctate lesions that are smaller and undetectable on SD-OCT. Both exhibit variable FAF intensities and are poorly visualized on IR. Eyes with drusen exhibited a slightly thicker RPE compared with control eyes (+3.4 µm, P=0.012). Genetic polymorphisms associated with drusenoid lesions in rhesus monkeys in ARMS2 and HTRA1 were similar in frequency between the two phenotypes. These results refine our understanding of drusen development, and provide insight into the absence of advanced AMD in nonhuman primates.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Drusas Retinianas / Degeneração Macular Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Drusas Retinianas / Degeneração Macular Idioma: En Ano de publicação: 2017 Tipo de documento: Article