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Symmetry of Bilateral Lesions in Geographic Atrophy in Patients With Age-Related Macular Degeneration
Caren Bellmann, MD;
Jork Jorzik, MD;
Georg Spital, MD;
Kristina Unnebrink, PhD;
Daniel Pauleikhoff, MD;
Frank G. Holz, MD
Arch Ophthalmol. 2002;120:579-584.
Background As a cause for severe visual loss, geographic atrophy of the retinal
pigment epithelium is about half as common as choroidal neovascularization
in patients with advanced age-related macular degeneration. To assess symmetry,
we determined intraindividual variations of various features of bilateral
geographic atrophy in patients with atrophic age-related macular degeneration
in a cross-sectional study.
Methods Patients were examined with the use of a confocal scanning laser ophthalmoscope
(Heidelberg Retina Angiograph; Heidelberg Engineering, Heidelberg, Germany).
Digital infrared reflection images (excitation, 830 nm) and fundus autofluorescence
images (excitation, 488 nm) were recorded. The eyes of each patient were compared
regarding number, size, and convex hull of the atrophic areas with the use
of image analysis software and with respect to fundus autofluorescence changes
in the junctional zone.
Results Seventy-two patients (mean ± SD age, 76.3 ± 7.9 years)
were examined. The number of atrophic areas ranged from 1 to 23 (mean ±
SD, 4.9 ± 4.6); the size of geographic atrophy, from 0.18 to 30.20
(mean ± SD, 7.0 ± 6.6) mm2; and the size of the convex
hull, from 0.18 to 39.20 (mean ± SD, 11.7 ± 8.4) mm2.
No statistically significant difference was found when comparing these variables
between each left and right eye: number, P = .62;
size, P = .81; and convex hull, P = .78. Identical patterns of fundus autofluorescence were observed
in 43 (80%) of 54 patients.
Conclusions There is intraindividual symmetry in eyes with bilateral geographic
atrophy in the presence of a wide range of interindividual variability. The
findings are in accordance with the view that age-related macular degeneration
is not merely the result of a nonspecific aging process. Symmetric manifestations,
rather, reflect specific individual determinants in the pathogenesis and manifestation
of the disease.
From the Department of Ophthalmology (Drs Bellmann, Jorzik, and Holz)
and the Coordination Centre for Clinical Trials (Dr Unnebrink), University
of Heidelberg, Heidelberg; and the Department of Ophthalmology, St Franziskus
Hospital, Münster (Drs Spital and Pauleikhoff), Germany.
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