Precursors and Development of Geographic Atrophy with Autofluorescence Imaging: Age-Related Eye Disease Study 2 Report Number 18.


Journal

Ophthalmology. Retina
ISSN: 2468-6530
Titre abrégé: Ophthalmol Retina
Pays: United States
ID NLM: 101695048

Informations de publication

Date de publication:
09 2019
Historique:
received: 21 11 2018
revised: 08 04 2019
accepted: 09 04 2019
pubmed: 4 6 2019
medline: 22 8 2020
entrez: 3 6 2019
Statut: ppublish

Résumé

To describe the sequence of events leading to development of geographic atrophy (GA) in age-related macular degeneration with fundus autofluorescence (FAF) imaging. Post hoc analysis of FAF images from the Age-Related Eye Disease Study 2. Fundus autofluorescence images of 120 eyes (109 patients) with incident GA and at least 2 years of preceding FAF images. Images of incident GA were stacked and aligned over FAF images of preceding annual visits. The regions of retina where incident GA developed were assessed on prior years' FAF images. These regions, defined as precursor lesions, were classified into minimal change autofluorescence, predominant hypoautofluorescence (decreased autofluorescence), predominant hyperautofluorescence (increased autofluorescence), and mixed autofluorescence. The natural progression in precursor lesions leading to GA formation and their associations with incident GA size and GA enlargement rate were evaluated. Incident GA area and enlargement rate and precursor pattern frequency. Incident GA had a mean area of 1.00 mm Using image registration, we identified changes in autofluorescence images before the onset of GA. Decreased autofluorescence was the most common change, although minimal changes also were seen in one third of the images. Incident GA that arises from predominantly normal autofluorescence is associated with faster enlargement rates compared with GA arising from abnormal autofluorescence. Faster GA enlargement rates also were associated with incident GA size, area of surround abnormal autofluorescence, and presence of reticular pseudodrusen.

Identifiants

pubmed: 31153849
pii: S2468-6530(18)30672-9
doi: 10.1016/j.oret.2019.04.011
pii:
doi:

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, N.I.H., Intramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

724-733

Informations de copyright

Copyright © 2019 American Academy of Ophthalmology. All rights reserved.

Auteurs

Ian C Holmen (IC)

Fundus Photographic Reading Center, University of Wisconsin, Madison, Wisconsin.

Bryce Aul (B)

Fundus Photographic Reading Center, University of Wisconsin, Madison, Wisconsin.

Jeong W Pak (JW)

Fundus Photographic Reading Center, University of Wisconsin, Madison, Wisconsin.

Ralph Moeller Trane (RM)

Fundus Photographic Reading Center, University of Wisconsin, Madison, Wisconsin.

Barbara Blodi (B)

Fundus Photographic Reading Center, University of Wisconsin, Madison, Wisconsin.

Michael Klein (M)

Casey Eye Institute, Oregon Health and Science University, Portland, Oregon.

Traci Clemons (T)

The Emmes Corporation, Rockville, Maryland.

Emily Chew (E)

Division of Epidemiology and Clinical Applications, National Eye Institute, National Institutes of Health, Bethesda, Maryland.

Amitha Domalpally (A)

Fundus Photographic Reading Center, University of Wisconsin, Madison, Wisconsin. Electronic address: domalpally@wisc.edu.

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Classifications MeSH