Progressing geographic atrophy: choroidal thickness and retinal sensitivity identify two clinical phenotypes
Elisabetta Pilotto1, Francesca Guidolin1, Enrica Convento1
1Department of Ophthalmology, University of Padova, Padova, Italy.
The British Journal of Ophthalmology
|February 14, 2015
Summary
Changes in choroidal thickness and retinal sensitivity differ between geographic atrophy (GA) patients with or without choroidal neovascularisation (CNV) in the fellow eye. This suggests distinct GA phenotypes and pathophysiologic mechanisms.
Area of Science:
- Ophthalmology
- Medical Imaging
- Retinal Diseases
Background:
- Geographic atrophy (GA) is a progressive form of age-related macular degeneration.
- Understanding GA progression and associated factors is crucial for developing effective treatments.
- The role of choroidal neovascularisation (CNV) in the fellow eye on GA progression is not fully understood.
Purpose of the Study:
- To analyze changes in choroidal thickness and retinal sensitivity (Se) in patients with geographic atrophy (GA).
- To compare these changes in patients with GA with and without choroidal neovascularisation (CNV) in the fellow eye.
Main Methods:
- Study included patients with bilateral GA (B-GA) and unilateral GA with CNV in the fellow eye (U-GA).
- Follow-up was conducted every 6 months, evaluating enhanced depth imaging optical coherence tomography (OCT), fundus autofluorescence (FAF), and microperimetry.
- Measurements included GA area, choroidal thickness, and retinal sensitivity (Se) at baseline and during follow-up.
Main Results:
- Mean GA area increased significantly in both groups during follow-up.
- Choroidal thickness was significantly greater in the B-GA group compared to the U-GA group at baseline and follow-up.
- Choroidal thickness decreased significantly only in the U-GA group, while retinal sensitivity (Se) decreased significantly only in the B-GA group.
Conclusions:
- Changes in retinal sensitivity and choroidal thickness differ between patients with GA with or without CNV in the fellow eye.
- These findings suggest at least two distinct GA phenotypes.
- The development and progression of GA may be driven by different pathophysiologic mechanisms in these phenotypes.
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