Visual function metrics in early and intermediate dry age-related macular degeneration for use as clinical trial endpoints

KJ Cocce, SS Stinnett, UFO Luhmann… - American journal of …, 2018 - Elsevier
KJ Cocce, SS Stinnett, UFO Luhmann, L Vajzovic, A Horne, SG Schuman, CA Toth
American journal of ophthalmology, 2018Elsevier
Purpose To evaluate and quantify visual function metrics to be used as endpoints of age-
related macular degeneration (AMD) stages and visual acuity (VA) loss in patients with early
and intermediate AMD. Design Cross-sectional analysis of baseline data from a prospective
study. Methods One hundred and one patients were enrolled at Duke Eye Center: 80
patients with early AMD (Age-Related Eye Disease Study [AREDS] stage 2 [n= 33] and
intermediate stage 3 [n= 47]) and 21 age-matched, normal controls. A dilated retinal …
Purpose
To evaluate and quantify visual function metrics to be used as endpoints of age-related macular degeneration (AMD) stages and visual acuity (VA) loss in patients with early and intermediate AMD.
Design
Cross-sectional analysis of baseline data from a prospective study.
Methods
One hundred and one patients were enrolled at Duke Eye Center: 80 patients with early AMD (Age-Related Eye Disease Study [AREDS] stage 2 [n = 33] and intermediate stage 3 [n = 47]) and 21 age-matched, normal controls. A dilated retinal examination, macular pigment optical density measurements, and several functional assessments (best-corrected visual acuity, macular integrity assessment mesopic microperimety, dark adaptometry, low-luminance visual acuity [LLVA] [standard using a log 2.0 neutral density filter and computerized method], and cone contrast test [CCT]) were performed. Low-luminance deficit (LLD) was defined as the difference in numbers of letters read at standard vs low luminance. Group comparisons were performed to evaluate differences between the control and the early and intermediate AMD groups using 2-sided significance tests.
Results
Functional measures that significantly distinguished between normal and intermediate AMD were standard and computerized (0.5 cd/m2) LLVA, percent reduced threshold and average threshold on microperimetry, CCTs, and rod intercept on dark adaptation (P < .05). The intermediate group demonstrated deficits in microperimetry reduced threshhold, computerized LLD2, and dark adaptation (P < .05) relative to early AMD.
Conclusions
Our study suggests that LLVA, microperimetry, CCT, and dark adaptation may serve as functional measures differentiating early-to-intermediate stages of dry AMD.
Elsevier