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Results for “Color Vision Defects”

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PubMed1999

Rods induce transient tritanopia in blue cone monochromats.

Transient tritanopia is a cone-cone post-receptoral interaction between short-wavelength (S) cones and medium (M) and long (L) wavelength cones. Blue cone monochromats have rods and S cones of normal sensitivity but lack functional M/L cones. All blue cone monochromats tested (n = 8) show significant amounts of transient tritanopia mediated by rods. Attempts to find a similar rod-S cone interaction while silencing the L/M cones in normals yielded only a small amount of S cone sensitivity loss. The results suggest an exaggerated influence of rods on the S cone pathway in the retina of blue cone monochromats.

Adaptation, Ocular↗
PubMed1999

Rod-cone-interactions in deuteranopic observers: models and dynamics.

We studied the interactions between rods and L-cones in deuteranopic human observers by stimulating the photoreceptors independently. Thresholds were determined using a PEST procedure for different ratios of rod to L-cone modulation without modulating the S-cones. Modulation frequency was either 2 or 10 Hz and the retinal illuminance ranged from 4.7 to 470 td (10.9-1090 scot td). We measured at 2, 7.5 and 20 degrees retinal eccentricity. The threshold data could be described by a model based on a vector addition of responses originating in the rods and the L-cones. The relative strength of rod signals relative to the L-cone signals increased with increasing retinal eccentricity and decreasing retinal illuminance. At 20 degrees eccentricity, rod and cone signals were of about equal magnitude at retinal illuminances as high as 470 td. Temporal frequency did not have a large effect on the ratio of rod to L-cone signal strength.

Adult↗
PubMed1999

L, M and L-M hybrid cone photopigments in man: deriving lambda max from flicker photometric spectral sensitivities.

Using heterochromatic flicker photometry, we have measured the corneal spectral sensitivities of the X-chromosome-linked photopigments in 40 dichromats, 37 of whom have a single opsin gene in their tandem array. The photopigments encoded by their genes include: the alanine variant of the normal middle-wavelength sensitive photopigment, M(A180); the alanine and serine variants of the normal long-wavelength sensitive photopigment, L(A180) and L(S180); four different L-M hybrid or anomalous photopigments, L2M3(A180), L3M4(S180), L4M5(A180) and L4M5(S180); and two variants of the L-cone photopigment, encoded by genes with embedded M-cone exon two sequences, L(M2; A180) and L(M2; S180). The peak absorbances (lambda max) of the underlying photopigment spectra associated with each genotype were estimated by correcting the corneal spectral sensitivities back to the retinal level, after removing the effects of the macular and lens pigments and fitting a template of fixed shape to the dilute photopigment spectrum. Details of the genotype-phenotype correlations are summarized elsewhere (Sharpe, L. T., Stockman, A., Jägle, H., Knau, H., Klausen, G., Reitner, A. et al. (1998). J. Neuroscience, 18, 10053-10069). Here, we present the individual corneal spectral sensitivities for the first time as well as details and a comparison of three analyses used to estimate the lambda max values, including one in which the lens and macular pigment densities of each observer were individually measured.

Adult↗
PubMed2000

Chromatic and luminance contributions to a hyperacuity task.

Displacement thresholds with incremental chromatic and luminance edges were measured on different backgrounds. Above 3% luminance contrast, thresholds were always similar. At luminance contrasts below 3%, luminance edges could not be detected, but chromatic edges were still visible. At these low contrasts displacement thresholds for chromatic edges increased to a high level. We interpret these data in terms of multiple mechanisms; above 3% contrast a luminance mechanism determines thresholds, but when, at lower contrasts, chromatic mechanisms support detection, they also support the spatial task. Physiological data were consistent with the different mechanisms originating at the retinal ganglion cell level.

Animals↗
PubMed2004

The primacy of chromatic edge processing in normal and cerebrally achromatopsic subjects.

The local chromatic contrast between surfaces in a visual scene plays an important role in theories of color perception. Our studies of cerebral achromatopsia suggest that this contrast signal is computed independently of the more complex processes such as edge integration and anchoring. We report a study in which we attempted to determine whether local-contrast signals also drove behavior in normal subjects. We sought to reduce the role of edge integration and anchoring by using stimuli whose background varied very gradually in color from top to bottom. The local chromatic contrast of patches relative to such backgrounds depends upon the position at which they are presented. It is therefore possible for patches with identical spectral composition to have opposite contrasts. We constructed stimuli in which two of three vertically arranged discs had the same contrast while the third had opposite contrast. The stimuli were also constructed so that the contrast-odd disc and one of the other two had identical spectral composition while the third disc had different composition. We used these stimuli in an attentional task where, after a brief delay, a letter discrimination target was presented in the location of one of the discs. Attention should automatically be attracted to the odd disc in such a display. Normal observers were faster at making the letter discrimination when the target appeared at the contrast-odd as opposed to spectrally odd location. We conclude that local chromatic contrast, but not raw spectral composition, is accessible to normal observers at an appropriate stage in visual processing to drive attention.

Adult↗
PubMed2001

Disc excavation in dominant optic atrophy: differentiation from normal tension glaucoma.

OBJECTIVE: In patients with dominant optic atrophy (DOA, Kjer type), excavation of the optic nerve develops, and these patients may be misdiagnosed as having normal tension glaucoma (NTG). This study examined disc morphologic features in patients with DOA and explored features that help distinguish this condition from NTG. DESIGN: Noncomparative, observational case series. PARTICIPANTS: Patients with DOA who were seen at the Duke University Eye Center between 1987 and 1996 and who had bilateral optic nerve photographs. METHODS: Retrospective chart review of the results of visual acuity testing, visual field testing by Goldmann perimetry, color vision testing, intraocular pressure measurement, and observation of bilateral optic nerve photographs. MAIN OUTCOME MEASURES: Appearance of the optic disc and peripapillary zone in patients with DOA. RESULTS: Nine patients were identified. The mean age at the time of evaluation was 28 years (range, 11-62 years). Most patients had a mild to moderate reduction in visual acuity. Color vision as tested with Hardy-Rand-Rittler plates was reduced (4.0/10 +/- 4.2/10). A cup-to-disc ratio of more than 0.5 was observed in at least one eye of eight patients. A temporal wedge-shaped area of excavation was observed in 14 of the 18 eyes studied. Moderate to severe temporal pallor was observed in all of the eyes. Pallor of the remaining (noncupped) neuroretinal rim was also observed consistently, ranging from mild to moderate. A gray crescent and some degree of peripapillary atrophy were noted in all eyes. CONCLUSIONS: Several clinical features, including early age of onset, preferential loss of central vision, sparing of the peripheral fields, pallor of the remaining neuroretinal rim, and a family history of unexplained visual loss or optic atrophy, help to distinguish patients with DOA from those with NTG.

Adolescent↗
PubMed1993

Fellow eye abnormalities in acute unilateral optic neuritis. Experience of the optic neuritis treatment trial.

BACKGROUND: Visual function in the fellow eye at the onset of unilateral optic neuritis has not been systematically evaluated. The authors prospectively determined the prevalence of abnormalities in the fellow eyes of the 448 eligible patients entered into the Optic Neuritis Treatment Trial. METHODS: All patients underwent testing of visual acuity, contrast sensitivity, color vision, and visual field, as well as magnetic resonance imaging (MRI) of the brain and a neurologic examination. RESULTS: Abnormalities in the fellow eye were found on measurement of visual acuity in 13.8%, contrast sensitivity in 15.4%, color vision in 21.7%, and visual field in 48.0% of patients. The majority of the fellow eye deficits resolved over several months. A higher prevalence of MRI changes consistent with demyelination of the brain was found in patients with a past history of optic neuritis in the fellow eye compared with patients without such a history (P = 0.004). Patients with abnormal fellow eyes but no history of previous optic neuritis were no more likely to have clinical (P = 0.658) or MRI evidence (P = 0.166) of multiple sclerosis than patients with normal fellow eyes. CONCLUSIONS: The improvement of many of the visual deficits indicates that visual abnormalities detected in the fellow eye at the onset of symptomatically unilateral optic neuritis may not represent preexisting optic nerve demyelination. Whether the presence of these deficits is predictive of the development of clinical multiple sclerosis cannot be determined at this time.

Acute Disease↗