Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/59012
Title: Correlation of Histologic Features with In Vivo Imaging of Reticular Pseudodrusen
Contributor(s): Greferath, Ursula (author); Guymer, Robyn H (author); Vessey, Kirstan A  (author)orcid ; Brassington, Kate (author); Fletcher, Erica L (author)
Publication Date: 2016
Open Access: Yes
DOI: 10.1016/j.ophtha.2016.02.009
Handle Link: https://hdl.handle.net/1959.11/59012
Abstract: 

Purpose: To determine the histologic and cellular correlates in the retina and retinal pigment epithelium (RPE) with the presence of optical coherence tomography-defined reticular pseudodrusen (RPD).

Design: Observation case using immunocytochemistry of an exenterated eye with immediate fixation after removal.

Participants: Two patients, one with confirmed RPD and the other with mid-peripheral drusen, underwent multimethod imaging before exenteration and immediate fixation of the posterior eyecup for high-resolution immunocytochemical analysis.

Methods: Optical coherence tomography (OCT) was compared with high-resolution immunocytochemistry using a range of cellular markers to determine changes in the RPE, photoreceptors, and gliosis.

Main Outcome Measures: Correlations of the appearance of reticular pseudodrusen on OCT and immunocytochemical analysis.

Results: Reticular pseudodrusen were deposits juxtaposed to photoreceptor outer segments extending through the outer nuclear layer and even beyond the outer limiting membrane. Deposits were rich in vitronectin, photoreceptor-associated proteins, and Iba1-immunoreactive immune cells. In contrast to conventional drusen the lipid stain Oil Red O failed to stain RPD. Cellular analysis revealed that RPD were associated with photoreceptor disruption and loss and localized gliosis. In addition, anomalies in the RPE were observed.

Conclusions: Reticular pseudodrusen represent subretinal deposits that extend through the outer nuclear layer, affect photoreceptor integrity, and are associated with retinal gliosis and RPE damage.

Publication Type: Journal Article
Source of Publication: Ophthalmology, 123(6), p. 1320-1331
Publisher: Elsevier Inc
Place of Publication: United States of America
ISSN: 1549-4713
0161-6420
Fields of Research (FoR) 2020: 320907 Sensory systems
321204 Vision science
Socio-Economic Objective (SEO) 2020: 280103 Expanding knowledge in the biomedical and clinical sciences
Peer Reviewed: Yes
HERDC Category Description: C1 Refereed Article in a Scholarly Journal
Appears in Collections:Journal Article
School of Science and Technology

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