Multifocal Pupillography in Early Age-Related Macular Degeneration

被引:27
|
作者
Sabeti, Faran [1 ,2 ]
Maddess, Ted [1 ,2 ]
Essex, Rohan W. [1 ,2 ,3 ]
Saikal, Aiasha [1 ,2 ]
James, Andrew C. [1 ,2 ]
Carle, Corinne F. [1 ,2 ]
机构
[1] Australian Natl Univ, ARC Ctr Excellence Vis Sci, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
[2] Australian Natl Univ, Ctr Visual Sci, John Curtin Sch Med Res, Canberra, ACT 0200, Australia
[3] Australian Natl Univ, Canberra Hosp, Dept Ophthalmol, Canberra, ACT 0200, Australia
基金
澳大利亚研究理事会;
关键词
multifocal; objective perimetry; pupils; age-related macular degeneration; ON-YELLOW PERIMETRY; FLICKER PERIMETRY; PUPIL PERIMETRY; VISUAL FUNCTION; EYE DISEASE; SENSITIVITY; TESTS; CONE;
D O I
10.1097/OPX.0000000000000319
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose. To investigate the potential of multifocal pupillographic objective perimetry to assess changes in retinal function with clinical severity of age-related macular degeneration (AMD). Methods. Pupil responses were recorded from 40 subjects with AMD and 23 normal control subjects (mean +/- SD age, 71.3 +/- 5.1 years). Age-related macular degeneration subjects were classified according to the Age-Related Eye Disease Study (AREDS) classification system and allocated into one of four AMD severity groups. Three multifocal pupillographic objective perimetry stimulus variants that were identical in luminance but varied in spatiotemporal sequence were used. In one of the three protocols, stimuli were presented with a pedestal flicker for 266 milliseconds at 15 Hz. Results. On average, response amplitudes demonstrated a significant change in sensitivity with progression from early-stage (0.32 +/- 0.08 dB, t = 3.88) to late-stage (-1.60 +/- 0.12 dB, t = -12.7) age-related macular degeneration. Response delays followed a similar trend with the longest delays in AREDS4 (57.2 +/- 1.9 milliseconds, t = 29.5). Ring analysis identified the largest mean effect on responses within the central 6 degrees of fixation. The NewStimuli protocol achieved the best diagnostic accuracy across all severity groups with area under the curve values of 0.85 +/- 0.066 (AREDS1), 0.908 +/- 0.085 (AREDS2), 0.929 +/- 0.040 (AREDS3), and 1.0 +/- 0.0 (AREDS4). Conclusions. The mean effect of AMD on contraction amplitudes and response delays reflected the severity of disease, and the NewStimuli protocol achieved good diagnostic accuracy across all AMD severity groups. Multifocal pupillographic objective perimetry may potentially be a useful method in monitoring progression of AMD and assessing change in retinal function with novel interventions in early AMD. Longitudinal studies are required to identify biomarkers that predict eyes at risk of progression.
引用
收藏
页码:904 / 915
页数:12
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