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Erschienen in: Documenta Ophthalmologica 2/2016

21.09.2016 | Original Research Article

Towards an electroretinographic assay for studying colour vision in human observers

verfasst von: Jan Kremers, Deepak Bhatt

Erschienen in: Documenta Ophthalmologica | Ausgabe 2/2016

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Abstract

Purpose

To determine whether electroretinograms (ERGs) to heterochromatic stimulation can detect and quantify hereditary colour vision deficiency.

Methods

ERGs were measured to counterphase modulation of red and green stimuli. The total modulation depth of the red and green stimuli was constant. The ratio of red to green modulation was varied, and the responses were measured at two temporal frequencies: 12 and 36 Hz. Subjects were 13 protanopes, 19 protanomalous trichromats, 38 deuteranopes, 16 deuteranomalous trichromats and 22 normal trichromats.

Results

The responses are in agreement with previous findings: they were determined by a vector additive input of L- and M-cones (and thus is luminance sensitive) at 36 Hz. At 12 Hz, the responses can be modelled a vector addition of an L-/M-additive response (as determined by the 36 Hz ERGs) and an L-/M-opponent response. From the models, L-cone input fraction (36 Hz) and luminance input fraction (12 Hz) were estimated. The five groups showed different characteristics. However, the signal-to-noise ratio (SNR) at 12 Hz was not always satisfactory.

Conclusions

The ERGs to heterochromatic stimuli are potentially interesting for determining the presence and the type of colour vision deficiencies, provided some measures are taken to improve the 12 Hz SNRs.
Fußnoten
1
It has been argued that parvocellular cells could also be the physiological basis for luminance vision and thus has a “double-duty”. In our opinion, there are two arguments against this proposition: First, it has been found that the psychophysical sensitivities to isoluminant chromatic stimuli decrease for frequencies above about 4 Hz although the opponent cells respond well to these stimuli at much higher frequencies. It therefore has been suggested that there is a cortical filter in the opponent channel. It is difficult to imagine how such a filter would not involve luminance signals from opponent cells, particularly because these luminance signals manifest themselves at very high temporal frequencies (typically above about 40 Hz as it is caused by the small centre-surround latency difference in opponent cells). Second, The L/M ratio in the luminance channel is larger than one, can (dependent on subject, stimulus size, position, etc.) be as large 10:1 and is correlated with the ratio of L- to M-cone numbers. The L/M ratio in the chromatic channel is, however, about unity. It is difficult to conceive how different psychophysical L/M ratios can result from one underlying physiological mechanism.
 
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Metadaten
Titel
Towards an electroretinographic assay for studying colour vision in human observers
verfasst von
Jan Kremers
Deepak Bhatt
Publikationsdatum
21.09.2016
Verlag
Springer Berlin Heidelberg
Erschienen in
Documenta Ophthalmologica / Ausgabe 2/2016
Print ISSN: 0012-4486
Elektronische ISSN: 1573-2622
DOI
https://doi.org/10.1007/s10633-016-9561-y

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