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(Investigative Ophthalmology and Visual Science. 2000;41:267-273.)
© 2000 by The Association for Research in Vision and Ophthalmology, Inc.

Psychophysical Evidence for Rod Vulnerability in Age-Related Macular Degeneration

Cynthia Owsley1, Gregory R. Jackson1, Artur V. Cideciyan2, Yijun Huang2, Stuart L. Fine2, Allen C. Ho2, Maureen G. Maguire2, Virginia Lolley1 and Samuel G. Jacobson2

1 From the Department of Ophthalmology, School of Medicine, University of Alabama at Birmingham, Alabama; and 2 Department of Ophthalmology, Scheie Eye Institute, University of Pennsylvania, Philadelphia.

PURPOSE. To determine whether there is rod system dysfunction in the central retina of patients with age-related macular degeneration (AMD).

METHODS. Dark-adapted sensitivity (500-nm stimulus) and light-adapted sensitivity (600 nm) were measured psychophysically at 52 loci in the central 38° (diameter) of retina in 80 patients with AMD, and results were compared with those from older adult normal controls. All dark-adapted data were corrected for preretinal absorption.

RESULTS. Mean field dark-adapted sensitivity was significantly lower in AMD patients as a group than in normal subjects. Within the AMD group were subsets of patients with normal mean dark- and light-adapted sensitivities; reduced dark-adapted sensitivities without detectable light-adapted losses; both types of losses; and, least commonly, only light-adapted losses. Regional retinal analyses of the dark-adapted deficit indicated the greatest severity was 2° to 4° or approximately 1 mm from the fovea, and the deficit decreased with increasing eccentricity.

CONCLUSIONS. These psychophysical results are consistent with histopathologic findings of a selective vulnerability for parafoveal rod photoreceptors in AMD. The different patterns of rod and cone system losses among patients at similar clinical stages reinforces the notion that AMD is a group of disorders with underlying heterogeneity of mechanism of visual loss. Dark-adapted macula-wide testing may be a useful complement to the more traditional outcome measures of fundus pathology and foveal cone-based psychophysics in future AMD trials.




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