Objective: To determine whether there are disturbances in the rod-mediated
kinetics of dark adaptation in early age-related maculopathy (ARM).
Design: Comparative, observational case series.
Participants: Twenty older adults with early ARM as defined by one or more
large (>63 mum) drusen, focal hyperpigmentation, or both, but no choroidal
neovascularization or geographic atrophy, and 16 adults in the same age ran
ge with none of these fundus features. All participants had 20/25 visual ac
uity or better in the tested eye.
Methods: Dark adaptation functions were measured using a modified Humphrey
Field Analyzer (Zeiss Humphrey Systems, Dublin, CA) to assess the rate of r
od-mediated sensitivity recovery at 12 degrees on the vertical meridian in
the inferior visual field after exposure to the equivalent of a 98% bleach,
Baseline (prebleach) scotopic sensitivity, visual acuity, contrast sensiti
vity, and photopic sensitivity were also measured.
Main Outcome Measures: Rod-cone break; second and third components of rod-m
ediated dark adaptation; time to baseline sensitivity; and baseline (preble
ach) scotopic sensitivity.
Results: Although their visual acuity was at least 20/25, patients with ear
ly ARM on average exhibited deficits in almost all rod-mediated parameters
of dark adaptation as compared with age-similar healthy participants. For e
xample, the rod-cone break was delayed approximately 10 minutes in early AR
M patients as compared with healthy participants. Age-related maculopathy p
atients were more likely to fall outside the normal reference range for var
iables representing dark adaptation kinetics than for steady-state visual f
unctions such as scotopic sensitivity, For example, 85% of ARM patients fel
l outside the normal reference range in at least one dark adaptation kineti
c parameter, whereas only 25% of ARM patients fell outside the normal refer
ence range for steady-state scotopic sensitivity.
Conclusions: Rod-mediated kinetic parameters of dark adaptation, which refl
ect the sensitivity recovery of the visual cycle, are disrupted early in AR
M pathogenesis, Ophthalmology 2001;108:1196-1202 (C) 2001 by the American A
cademy of Ophthalmology.