ArticleInvestigative ophthalmology & visual science2024
Longitudinal Changes of Visual Sensitivity With Geographic Atrophy Progression Assessed by Defect-Mapping Microperimetry.
Article in Investigative ophthalmology & visual science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed.
- How "Micro" Is Microperimetry? Characterizing the Effect of Fundus Tracking on the Psychometric Function.Investigative ophthalmology & visual science · 2026Article
- Test-Retest Repeatability of a Novel Photopic Microperimetry Approach in Patients with Geographic Atrophy.Ophthalmology science · 2026Article
- Geographic Atrophy Structure-Function Relationships Based on Loss of OCT Outer Retinal Bands and Fundus Autofluorescence.Ophthalmology science · 2026Article
- Visual Function Assessment in Geographic Atrophy: A Review.Clinical & experimental ophthalmology · 2026Review
- Natural History of Visual Function Changes Over Three Years in Normal Aging and in Early and Intermediate Age-Related Macular Degeneration: ALSTAR2.Translational vision science & technology · 2026Article
- Geographic atrophy: Understanding the relationship between structure and function.Asia-Pacific journal of ophthalmology (Philadelphia, Pa.)Review
- Investigating Macular Tissue Integrity Index as a Novel Biomarker in Geographic Atrophy.Ophthalmology scienceArticle
- Customized Evaluation of Progressive Visual Sensitivity Loss in Geographic Atrophy to Improve the Power of Clinical Trials.Ophthalmology scienceArticle
- Targeted Defect-Mapping Microperimetry in Geographic Atrophy: A Sensitive Functional Outcome Measure for Intervention Trials.Ophthalmology scienceArticle
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Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
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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