TY - JOUR
T1 - Visual function tests as potential biomarkers in age-related macular degeneration
AU - Dimitrov, Peter
AU - Robman, Liubov
AU - Varsamidis, Mary
AU - Aung, Khin Zaw
AU - Makeyeva, Galina A
AU - Guymer, Robyn Heather
AU - Vingrys, Algis
PY - 2011
Y1 - 2011
N2 - Purpose. To evaluate the potential of psychophysical assessments of retinal function to provide diagnostic biomarkers of early age-related macular degeneration (AMD). Methods. Unilateral visual function was assessed in 221 participants (72.86 ? 9.94 years; 67 women) with early AMD (visual acuity better than 20/60) and 109 controls (73.07 ? 10.32 years; 65 women). Psychophysical assessment included steady state thresholds (4- and 14-Hz flicker and red and blue color) and dynamic tests (photostress recovery [PSR] and dark adaptation [DA]). All test parameters were compared in terms of their diagnostic capacity (sensitivity and specificity), reproducibility, and clinical applicability (test duration and participant s perception of test difficulty). AMD status was determined by digital photography, according to the International Classification and Grading System. Results. All functional measurements were significantly worse, on average, in the AMD group than in the control group (P <0.001). Static and dynamic parameters showed weak correlations (range, 0.003-0.225). Rod recovery in DA and cone recovery in PSR had the best diagnostic capacity (area under curve [AUC], receiver operating characteristic [ROC] analysis, 0.93 ? 0.016 and 0.85 ? 0.021, respectively). Considering diagnostic capacity together with test reproducibility and clinical applicability, the 14-Hz flicker gave the best outcome, followed by PSR. Combination of these two tests detected 71 of abnormal early AMD cases. Conclusions. All the visual function tests had good diagnostic capacity. Combination of the 14-Hz flicker thresholds and dynamics of the PSR test provided optimal quantitative assessment of retinal function in early AMD, suggesting that this set is a potentially useful clinical tool for following progression of early AMD and assessing the efficacy of interventions.
AB - Purpose. To evaluate the potential of psychophysical assessments of retinal function to provide diagnostic biomarkers of early age-related macular degeneration (AMD). Methods. Unilateral visual function was assessed in 221 participants (72.86 ? 9.94 years; 67 women) with early AMD (visual acuity better than 20/60) and 109 controls (73.07 ? 10.32 years; 65 women). Psychophysical assessment included steady state thresholds (4- and 14-Hz flicker and red and blue color) and dynamic tests (photostress recovery [PSR] and dark adaptation [DA]). All test parameters were compared in terms of their diagnostic capacity (sensitivity and specificity), reproducibility, and clinical applicability (test duration and participant s perception of test difficulty). AMD status was determined by digital photography, according to the International Classification and Grading System. Results. All functional measurements were significantly worse, on average, in the AMD group than in the control group (P <0.001). Static and dynamic parameters showed weak correlations (range, 0.003-0.225). Rod recovery in DA and cone recovery in PSR had the best diagnostic capacity (area under curve [AUC], receiver operating characteristic [ROC] analysis, 0.93 ? 0.016 and 0.85 ? 0.021, respectively). Considering diagnostic capacity together with test reproducibility and clinical applicability, the 14-Hz flicker gave the best outcome, followed by PSR. Combination of these two tests detected 71 of abnormal early AMD cases. Conclusions. All the visual function tests had good diagnostic capacity. Combination of the 14-Hz flicker thresholds and dynamics of the PSR test provided optimal quantitative assessment of retinal function in early AMD, suggesting that this set is a potentially useful clinical tool for following progression of early AMD and assessing the efficacy of interventions.
UR - http://www.iovs.org/content/52/13/9457.full.pdf+html
U2 - 10.1167/iovs.10-7043
DO - 10.1167/iovs.10-7043
M3 - Article
SN - 0146-0404
VL - 52
SP - 9457
EP - 9469
JO - Investigative Ophthalmology and Visual Science
JF - Investigative Ophthalmology and Visual Science
IS - 13
ER -