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PubMed1981

Scaling of color sensation by magnitude estimation: a contribution to opponent-colors theory.

Saturation and hue perceived in monochromatic stimuli and in light mixtures were scaled psychophysically by a direct magnitude estimation method. The colors were of aperture mode and were presented against a dark background. As a result opponent-colors functions were obtained which show the hue sensations produced by the lights of the visible spectrum (under the observing conditions used). Compared to the opponent-colors functions of Hurwich and Jameson, obtained by a cancellation technique, the subjective hue sensation differed significantly. It may be concluded that these cancellation functions describe an earlier, probably a retinal level of data processing, while our results may be regarded as a description of the output of the color vision system.

Color Perception↗
PubMedDate not supplied

Changes of color vision in ocular hypertension.

Fifty-six ocular hypertension (OHT) patients were examined for 2-3 days in the Eye Clinic of Kuopio University Hospital. No glaucomatous changes were found. Twenty-seven of them were found to have several risk factors for developing glaucoma and medication was started. Twenty-nine of the patients did not show risk factors and had no medication. Color vision was examined with the Farnsworth-Munsell 100 (FM 100) hue test and Besançon anomalometer, later Color Vision Meter 712 at the beginning of the study and 3 years later. None of the 56 patients showed any glaucomatous changes after 3 years of the study. In the treatment group, the FM 100 test showed significantly (paired t-test, p = 0.004) improved error scores after 3 years. In the non-treatment group, 19 patients did not develop risk factors; they had no significant changes in the color vision results. In 10 patients of the non-treatment group, risk factors had developed with elevated intraocular pressure and medication was started for them after 3 years. Their color vision results in the blue anomalous quotient (AQ) of the anomalometer had significantly shifted to the blue part of the equation (paired t-test, p = 0.04). The other color vision results had not changed significantly. The significantly improved FM 100 scores in the treatment group could mean, that the treatment has a beneficial effect for the OHT eyes at risk for developing glaucoma.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗
PubMed1997

Large-field S-cone flicker test.

BACKGROUND: Disturbances of blue color vision and of temporal contrast sensitivity can indicate early damage in glaucoma. For the present study a quick and easy test was devised which examines both functions at one time by testing the temporal contrast sensitivity of a blue flickering light on an intense yellow background. METHODS: Large coextensive background and test fields (85 degrees) are used, making fixation uncritical. Detailed experiments were made in two normal subjects to derive spectral sensitivity curves from flicker-fusion frequency (FFF) versus intensity functions and to obtain complete temporal contrast-sensitivity (De Lange) curves under different levels of adaptation and test lights. After selection of appropriate luminances and one stimulation frequency from these experiments, test-retest variability was studied in four subjects in five repetitions. In addition, normal values were collected from 22 subjects. RESULTS: Spectral sensitivities for two levels of FFF (15 Hz and 44 Hz) agree with Stiles' pi 1 at the low and with pi 4 at the high FFF. Temporal contrast-sensitivity curves show a low-frequency section with peak sensitivity at 1 Hz and a high-frequency section with a peak at around 4 Hz. From the basic experiments the following conditions for the clinical examination were selected: Background luminance 2600 cd/m2, test luminance at 451 nm 0.8 cd/m2, stimulation frequency 4 Hz. The test-retest variability showed an acceptable intraclass correlation co-efficient (0.6). CONCLUSIONS: The present experiments carried out with a very large stimulus led to meaningful results which are in rather good agreement with results reported in the literature on small-field stimuli. The blue-on-yellow flicker test carried out under the conditions mentioned above is a quick and easy test which could be helpful in improving early glaucoma diagnosis.

Adaptation, Ocular↗
PubMedDate not supplied

Comparative neurobiology of color vision in humans and animals.

Discrimination of colors was studied using an instrumental learning paradigm in monkeys (Macaque rhesus) and fishes (Carpio cyprinus L.). The confusion matrices composed of probabilities of instrumental responses were treated by factor analysis. The spherical structure of perceptual color space revealed in both animals was similar to that in humans. The four eigenvectors constituting the four-dimensional Euclidean hypersphere correspond to "red-green," "blue-yellow," "brightness," and "darkness" neuronal channels.

Animals↗
PubMed2001

Colour discrimination impairment is not a reliable early marker of Parkinson's disease.

Disturbances of colour visual discrimination have been shown to occur frequently in Parkinson's disease (PD). To verify the potential utility of reduced colour sensitivity as a diagnostic marker of early PD, we examined 14 PD patients, mean age 55.4 years, disease duration 2.3 years, in Hoehn and Yahr stages 1, 1.5, or 2, previously untreated with levodopa. Colour discrimination was measured with the Farnsworth-Munsell 100-hue test in patients who were compared with age-matched controls. The examinations were performed under standard conditions in a room illuminated by a daylight lamp Biolux Osram 6500 K. The mean total error score (MTES) and partial error scores (green-yellow and red-green axis) were calculated for every person examined. No significant differences were found between PD patients (MTES 49.1 +/- SD 37) and controls (MTES 37.9 +/- SD 25). Similarly, the mean partial scores were not significantly elevated in PD patients. We found an elevation of error scores exceeding the upper limit of normality (control mean + 2SD) only in three patients. We conclude that colour visual discrimination is not consistently impaired in early stages of PD and does not appear as a reliable early marker of Parkinson's disease.

Adult↗
PubMed1975

Best's vitelliform macular dystrophy.

A patient with Best's vitelliform macular dystrophy in his right eye had an intact vitelliform disk and drusen of the optic papilla. Although the foveola elevated by a few tenths of a millimeter, resolution was only slightly affected and the retinal receptors remained remarkably well-aligned, suggesting that mechanisms subserving receptor alignment still functioned. Hue discrimination and visual acuity were only slightly affected and the electroretinogram and visually evoked response showed essentially normal values. The vitelliform disk in the left eye ruptured by direct, blunt trauma. This same eye later developed subretinal macular neovascularization, as its visual acuity reduced, retinal sensitivity decreased, receptor orientation showed abnormalities, and hue discrimination became less efficient; the electroretinogram and visually evoked response remained normal.

Accommodation, Ocular↗
PubMed1982

Annular macular dystrophy.

Of 21 individuals from three generations of a single family with annular macular dystrophy, six showed only dyschromatopsia, one had dyschromatopsia and foveal hyperpigmentation, and four individuals had dyschromatopsia, foveal hyperpigmentation, and perifoveal circular pigment epithelial atrophy. Normal findings obtained on electrophysiologic testing suggest that this is a focal (macular) disorder rather than a generalized fundus disorder.

Adolescent↗
PubMed1996

Ishihara test performance and dementia.

Ishihara trail-tracing (TT) and number-naming (NN) tests were administered to a clinical sample of 378 demented patients. Error counts on TT and NN tests were best fit by a negative binomial (overdispersed Poisson) distribution. TT, NN, and combined (TT + NN) error counts were regressed on patient characteristics (sex, age, and education), severity of cognitive impairment (Mini-Mental State Exam: MMSE), dementia stage (Clinical Dementia Rating: CDR), etiology, onset age, and symptom duration in a negative binomial generalized linear model. Patient characteristics, onset age, and symptom duration had no significant effects on any error count. The effects of MMSE, CDR, and etiology, on the other hand, were highly significant and appear to help discriminate vascular dementia from Alzheimer's disease. MMSE (which taps cognitive skills) correlated with both TT and NN errors. CDR (which taps both cognitive and functional skills) correlated only with TT errors and dementia etiology correlated only with NN errors. These distinct correlational patterns reflect differences between the TT and NN tasks (i.e., trail-tracing vs. number-naming) related to specific brain loci and associated functions. This aspect of the phenomenon suggests that Ishihara tests have useful clinical applications in dementia.

Aged↗
PubMed1993

Investigations of the functional anatomy of attention using the Stroop test.

In two separate experiments positron emission tomography (PET) was used to measure changes in regional cerebral blood flow while normal subjects performed the Stroop colour word interference test, a test of selective attention. In the first experiment performance of the Stroop task was associated with activation of right orbito-frontal and bilateral parietal structures, an unexpected result in view of previously reported findings. In addition, there were highly significant time related focal changes in rCBF. A second experiment was therefore carried out which altered the experimental parameters to replicate an earlier study. In this second experiment focal activation of the right anterior cingulate and right frontal polar cortex occurred during the Stroop task. As in the first experiment significant time effects were again apparent. To determine the functionally related brain systems during the performance of the Stroop task a correlation analysis was carried out in relation to blood flow changes induced by experimental manipulation in the right anterior cingulate. This analysis indicated the engagement of a widespread network of anterior brain regions and reciprocal inhibition of posterior brain regions during the performance of the task. The results provide evidence for the involvement of anterior right hemisphere and medial frontal structures in attentional tasks but also indicate that time effects can confound task specific activations. Furthermore subtle experimental treatment parameters, such as stimulus presentation rate, influence the degree and distribution of observed activations.

Adult↗