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Purpose: To determine the relationship between structural and functional changes over time in the progression of geographic atrophy (GA) as assessed by defect-mapping microperimetry, an approach optimized to characterize the spatial extent of deep visual sensitivity losses.
Methods: A total of 57 eyes from 50 participants underwent defect-mapping microperimetry testing of the central 8° radius (with a 10-dB stimuli presented once each at 208 locations) over a median of five visits, scheduled at 3-monthly intervals. GA lesion(s) on fundus autofluorescence in the corresponding region tested on microperimetry at each visit were manually annotated.
Results: At a global level, change of GA extent in the central 8° radius explained a large proportion of the variance in the change in the proportion of locations missed (nonresponse) on defect-mapping microperimetry (R2 = 0.52). Locally, test locations that were entirely outside or within GA lesion(s) had a 0.3% (P = 0.305) and 2.3% (P < 0.001) probability of worsening between the two visits, respectively. In contrast, test locations with a 0% to 25%, 25% to 50%, 50% to 75%, or 75% to 100% change in the extent of GA overlapping between visits had a 4.1%, 12.0%, 17.5%, and 37.9% probability of worsening, respectively (all P < 0.001).
Conclusions: This study confirms that longitudinal changes in GA extent are associated with functional changes on defect-mapping microperimetry, both on a global and local level. These findings highlight the expected functional relevance of GA progression, and demonstrates the potential effectiveness of this microperimetry testing strategy for capturing visual function decline associated with GA progression.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11622159 | PMC |
http://dx.doi.org/10.1167/iovs.65.14.13 | DOI Listing |
Ophthalmol Sci
June 2025
Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, East Melbourne, Australia.
Purpose: To evaluate the effectiveness of targeted defect-mapping microperimetry (DMP) for capturing progressive visual function loss in eyes with a small extent of geographic atrophy (GA).
Design: Prospective longitudinal study.
Participants: Twenty-seven eyes from 25 participants with <0.
Br J Ophthalmol
June 2025
Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia
Background/aims: To examine the association between artificial intelligence (AI)-driven segmentation of geographic atrophy (GA) on optical coherence tomography (OCT) and visual sensitivity loss quantified by defect-mapping microperimetry, a testing strategy optimised to quantify the spatial extent of deep visual sensitivity losses.
Methods: 50 individuals with GA secondary to age-related macular degeneration underwent defect-mapping microperimetry testing within the central 8° radius region in one eye. GA on OCT was automatically segmented with an AI-based multiclass classification and segmentation model, and GA on fundus autofluorescence (FAF) images was manually annotated.
Ophthalmol Sci
March 2025
Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, East Melbourne, Australia.
Purpose: To evaluate the effectiveness of different approaches for customizing the selection of a subset of test locations on defect-mapping microperimetry (DMP) for improving the detection of progressive visual function decline in geographic atrophy (GA).
Design: Prospective longitudinal study.
Participants: Sixty eyes from 53 participants with GA secondary to age-related macular degeneration.
Invest Ophthalmol Vis Sci
December 2024
Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, East Melbourne, Australia.
Purpose: To determine the relationship between structural and functional changes over time in the progression of geographic atrophy (GA) as assessed by defect-mapping microperimetry, an approach optimized to characterize the spatial extent of deep visual sensitivity losses.
Methods: A total of 57 eyes from 50 participants underwent defect-mapping microperimetry testing of the central 8° radius (with a 10-dB stimuli presented once each at 208 locations) over a median of five visits, scheduled at 3-monthly intervals. GA lesion(s) on fundus autofluorescence in the corresponding region tested on microperimetry at each visit were manually annotated.
Invest Ophthalmol Vis Sci
January 2024
Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, East Melbourne, Australia.
Purpose: To examine the structure-function relationship in eyes with geographic atrophy (GA) using defect-mapping microperimetry, a testing strategy optimized to quantify the spatial extent of deep visual sensitivity losses.
Methods: Fifty participants with GA underwent defect-mapping microperimetry testing of the central 8°-radius region (208 locations tested once with a 10-decibel stimuli) and fundus autofluorescence imaging in one eye. The GA extent in the corresponding central 8°-radius was derived by manual annotations and image co-registration to examine the global structure-function relationship.