Yellow-blue Discrimination Research Articles

Impact of blur on clinical and occupational colour vision test results.

To evaluate whether colour vision normal (CVN) adults pass two Fletcher-Evans (CAM) lantern tests and to investigate the impact of imposed blur on Ishihara, CAM lantern and computerised colour discrimination test (colour assessment and diagnosis test [CAD] and Cambridge colour test [CCT]) results. In a pilot experiment, 20 (16 CVN and 4 colour vision deficient [CVD]) participants with normal VA were tested with the CAM lantern. In the main experiment, the impact of imposed dioptric blur (up to +8.00 D) on visual acuity and the Ishihara test, CAM lantern, CAD and CCT was assessed for 15 CVN participants. CVN participants can fail the CAM lantern, with specificity of 81.25% (aviation mode) and 75% (clinical mode), despite following the test requirements of participants having at least 0.18 logMAR (6/9) in the better eye. With blur, test accuracy was affected. As expected, significant detrimental effects of blur on test results were found for logMAR VA and CAM lantern (aviation) with +1.00 D or higher. Ishihara, CAD and CCT results were not detrimentally affected until +8.00 D. Yellow-blue discrimination was more affected by blur for the CAD than the CCT, which was not explained by the different colour spaces used or vectors tested. False-positive findings on lantern colour vision tests with small apertures are likely to be increased in patients with blur due to uncorrected refractive error or ocular and visual pathway disease. Other colour vision tests with larger stimuli are more robust to blur.

Cerebral achromatopsia

AbstractChromatic sensitivity was assessed in patients with pregeniculate and postgeniculate lesions. We examine changes in central vision along at foveal fixation and in each of the four paracentral quadrants of the visual field using the Colour Assessment and Diagnosis (CAD) test, a dynamic luminance contrast masking technique that isolates the use of Red / Green (RG) and Yellow / Blue (YB) colour signals. Because the extraction of colour signals in early visual processing involves opponent mechanisms, subjects with congenital RG loss of sensitivity exhibit symmetric increase in thresholds towards the long wavelength (“red”) and middle wavelength (“green”) regions of the spectrum locus. This is also frequently the case with acquired loss of chromatic sensitivity as a result of retinal or optic nerve disease. The findings from this study represent an exception to this rule. The patients investigated showed a marked asymmetry in colour thresholds. The study reveals how discrete, localized damage to visual pathways can cause selective loss of visual function and how the latter varies with retinal topography.The 36 pregeniculate patients investigated exhibited impairment in both RG and YB. Loss of colour vision was symmetrical for both RG and YB discrimination. Some pregeniculate patients exhibited substantial loss of colour vision in areas where perimetric loss was largely absent. All quadrants revealed similar symmetric loss of colour sensitivity.In 23 patients with postgeniculate lesions, patients with pre‐striate damage exhibited symmetric loss of chromatic sensitivity which affected either one or both chromatic mechanisms. Striate or extra‐striate lesions tended to exhibit general loss of colour vision within the area identified by visual field testing. More specific chromatic loss was associated with less impaired areas that were often normal on perimetric testing. Some patients with striate or extra‐striate lesions presented with asymmetric chromatic loss for one or more colour categories. When striate or extra‐striate lesions were also accompanied by underlying pre‐striate damage, chromatic sensitivity loss was always symmetric.The findings from this study show that the loss of chromatic sensitivity in cerebral achromatopsia depends strongly on the exact location and extent of the lesion with significant variation over the visual field. The same subject can exhibit loss of chromatic sensitivity that is either RG or YB specific, but also, spatially localized, non‐opponent loss of sensitivity for primary colours.

Loss of chromatic sensitivity in AMD and diabetes: a comparative study

Abnormalities in rod and cone photoreceptor morphology have been reported in normal aging retinas in the absence of known pathology and have been taken as an indicator of susceptibility to retinal disease. Some loss of visual performance may therefore precede retinal structural changes that can be detected reliably using conventional fundus imaging techniques. Red/green (RG) and yellow/blue (YB) colour discrimination thresholds are sensitive measures of normal retinal function and poor YB discrimination is often taken as an indicator of retinal disease, though it is generally acknowledged that RG loss is also present in most cases of acquired deficiency. Although structural changes in age-related macular degeneration (AMD) and diabetes share some similarities, significant differences remain and this may result in different patterns of RG and YB loss. The aim of this study was to quantify and compare the severity of RG and YB loss of chromatic sensitivity in patients with AMD and diabetes. Patients with varying severity of AMD and diabetes and normal subjects of similar age were recruited for the study. RG and YB colour detection thresholds were measured in the two groups of patients and the control group, using the Colour Assessment and Diagnosis (CAD) test. Each AMD subject investigated showed significant, but unequal loss of YB and RG chromatic sensitivity, with YB discrimination showing the greatest loss. Diabetic subjects also exhibited reduced chromatic sensitivity, but with almost equal and highly correlated RG and YB thresholds (R(2) = 0.99). The severity of colour vision loss measured with the CAD test also correlates well with a clinical classification index of disease progression in AMD, and with the level of hyperglycaemic control in diabetes. These findings suggest that accurate measurements of RG and YB colour thresholds can provide a sensitive measure of functional change in diseases of the retina with patterns of loss that differ significantly in AMD and diabetes.

Differential effects of ageing on foveal and peripheral colour vision

Abstract Purpose Colour sensitivity was assessed to establish aging effects both at the fovea and 6 deg away from fixation, in each of the four quadrants. Methods 65 normal healthy subjects (from 20 to 80 years of age) took part in the study. All subjects had Visual Acuity (VA) of 6/6 or better. Fixation accuracy was monitored using infrared imaging of the pupil and the tests were carried out on the P_SCAN system. Target size was adjusted for parafoveal locations to account for retinal and cortical magnification. Yellow‐blue (YB) and red‐green (RG) colour discrimination was assessed using the CAD (colour assessment and diagnosis) test (http://www.caa.co.uk/docs/33/200904.pdf). Results RG and YB colour thresholds were analysed separately for all five locations tested and showed no significant effect with ageing below the age of 60 years. Two age bands were formed based on statistical analysis (20‐59.9 and 60‐79.9). The decline in performance with age was more rapid at the fovea and exhibited a steeper gradient when compared with results in the periphery for both RG and YB discrimination. Foveal YB discrimination showed the largest ageing effect. No significant difference was found between the four parafoveal locations. YB discrimination at the fovea also exhibited the largest inter‐subject variability. Conclusion These findings may have clinical significance in the very early detection of disease processes that remain subclinical in many subjects. Differences between foveal and peripheral locations help to differentiate between the normal effects of ageing and disease. For example, higher foveal and normal peripheral YB thresholds in normal subjects from high peripheral thresholds in early glaucomatous subjects.

Fluctuation theory of colour discrimination of normal trichromats

The De Vries and Rose hypothesis concerning visual discrimination has been extended to the colour discrimination of normal trichromats. This hypothesis states that a luminance difference ΔB is just above threshold when ΔB just exceeds the statistical fluctuations in background luminance B, which are proportional to B 12 The colour difference required for the threshold is related to the statistical fluctuations in the rates of absorption of quanta by the three colour components in the visual system. A revision of the Thomson-Wright curves has been used as an estimate of the three cone sensitivity curves. A derivation of the shape of these curves is given in an appendix. A transformation from the Young-Helmholtz scheme into the Hering scheme is introduced to account for the independent variation of red-green and yellow-blue discrimination with visual angle Furthermore it is assumed that with increasing luminance the blue system has to be given an increasing weight in hue discrimination. This has been experimentally verified with a deuteranope. The apparent tritanomaly of normal subjects at low luminance has to be considered as a case of pseudotritanomaly. A satisfactory description of wavelength discrimination at low and high luminance and of the MacAdam ellipses is derived from this theory.