Electroretinograms following short-term chromatic light adaptation in high myopes and non-myopes
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Date
2025-10-17
Authors
Advisor
Choh, Vivian
McCulloch, Daphne
McCulloch, Daphne
Journal Title
Journal ISSN
Volume Title
Publisher
University of Waterloo
Abstract
Purpose: Worldwide, myopia cases are on the rise and the need for finding a definitive
mechanism by which myopia develops has become more imperative than ever before.
Axial elongation in myopic eyes is linked to short wavelength (λ) light-dependent increases
in retinal dopamine (DA). DA is associated with enhanced electroretinogram (ERG) amplitudes.
This thesis seeks to examine short-term adaptation to short and long λ light at
moderate and strong levels. I hypothesize that short λ light exposure differentially affects
full-field ERGs (ffERGs) and central ERGs in myopic eyes compared to controls.
Methods: In a multi-visit cross-over design, we compared ERGs before and after
20 minutes of full-field adaptation to long (red LED peak λ (λ 627 nm) or short (blue
LED peak λ 448 nm) λ light (Espion ColorDome™, Diagnosys LLC). Human participants
(ages 18-30) were healthy high myopes (≤-5 diopters (D)) and emmetropes (+1 D to -
0.25 D). Monocular, light-adapted (LA) ffERGs were recorded using skin electrodes and a
handheld system that adjusted for pupil diameter in real time (RETeval™). ERG stimuli
were LA standard white flash and flicker (85 Td.s), presented at 2 and 28.3 Hz, respectively.
The a-wave, b-wave and flicker ERG amplitudes, and implicit times were compared as
a function of pre/post adaption (time), adapting stimulus (λ), and refractive error (RE)
group using a mixed model ANOVA. Monocular multi-focal ERGs (mfERGs; 61 hexagons)
and pattern ERGs (PERGs; 15° field, 15’ reversing checks) were recorded with natural
pupils in keeping with ISCEV standards using DTL electrodes. The Espion™ console and
amplifier (Diagnosys LLC) was used for both ERG tests. The primary outcome measures
analyzed were the amplitudes and implicit times of the mfERG central wavelet, mfERG
average of the surrounding rings and the PERG P50 peak and were compared as a function
of pre/post adaption (time), adapting stimulus (λ), and RE group using a mixed model
ANOVA.
Results: There were no significant differences between controls and myopes prior to
adaptation (all p≥0.05) for ffERG tests. The luminance of the light had an effect such
that changes in b-wave implicit time decreased with adaptation to 300 cd/m² light in
controls (blue 30: -0.451 ± 1.28%; blue 300: -2.28 ± 2.56%; p≤0.001, η2G=0.14) but less
so in the high myope group (blue 30: +0.05 ± 1.3%; blue 300: -1.26 ± 2.43%; p=0.01,
η2G=0.05). Changes in flicker implicit time decreased with the stronger luminance level
but were not different between refractive error groups (i.e. controls: blue 30: 0.15 ± 1.0%;
blue 300: -1.05 ± 1.61%, myopes: blue 30: +0.44 ± 2.74%; blue 300: -1.1 ± 1.50%,
p≤0.001, η2G=0.13). Stronger light conditions caused b-wave amplitudes to become less
negative (smaller) (i.e. controls: blue 30: –5.38 ± 15.6%; blue 300: –3.50 ± 17.7%, myopes:
blue 30: –10.9 ± 15.4%; blue 300: +0.85 ± 10.9%, p=0.02, η2G=0.05). Similarly, with
v
flicker amplitudes, they became less negative (smaller) with stronger luminance adaptation
(i.e. controls: blue 30: –4.1 ± 13.4%; blue 300: –0.62 ± 17.1%, myopes: blue 30: –9.9 ±
18.3%; blue 300: +4.7 ± 12.0%, p=0.00, η2G=0.07). When comparing between controls
and high myopes or between short and long wavelengths, changes in b-wave amplitudes
did not differ. There was a significant difference between RE groups for the PERG P50
amplitude prior to adaptation (p=0.03; Cohen’s d=1.06) such that they were significantly
smaller in myopes (2.63 ± 1.0 μV) than controls (3.95 ± 1.5 μV). The N95 amplitudes
were also smaller (i.e. less negative) in myopes (-4.39 ± 1.82 μV) than controls (-6.58 ±
1.55 μV; p= 0.01; Cohen’s d=-1.3). The mfERGs showed no significant pre-adaptation
RE differences (all p≥ 0.05; all η2G≤ 0.07). For the PERG, in both controls and myopes,
the change in N95 amplitudes decreased more with long λ light (controls: -16.6 ± 23.4%;
myopes: -24.7 ± 43.4%) than short λ light (controls: +10.4 ± 23.5%; myopes: +1.88 ±
26.7%; p≤ 0.001; η2G=0.541). There were no effects of adaptation on the P50 amplitude
or implicit time. For mfERG, the change in N1P1 magnitude was not different between
controls and myopes and was not different when comparing λs for any of the five rings (p≥
0.05).
Conclusions: There is no evidence that chromatic adaptation has a differential effect
on post-adaptation ffERGs in high myopes. Long λ adaptation, especially with stronger
luminance, prolongs ERG implicit times, probably reflecting relatively reduced input from
the faster long cone system. There is evidence to suggest smaller central retinal responses
with the PERG P50 but not with the central wavelet of the mfERG, indicating altered
retinal ganglion cell function but not altered central inner retinal function in young adults
with myopia. Further studies should focus on confirming whether altered central retinal
function persists in adult myopes and whether longer adaptation times would yield a greater
RE difference.
Description
Keywords
blue light, high myopia, electroretinograms, chromatic light adaptation, short-term light adaptation