Mechanisms underlying the detection of increments in parafoveal retina

AbstractIt is well established that the spectral sensitivity under photopic conditions varies across the human retina. We investigate the mechanisms underlying these spectral changes. Through the use of color appearance, flicker sensitivity, additivity, discrimination at threshold and modeling, we show that the changes in spectral sensitivity on a photopic white background across parafoveal retina are consistent with shifts in cone weightings to (LM) and (ML) chromatic channels. This two channel model, developed to account for foveal spectral sensitivity curves (Sperling & Harwerth, 1971 Science, 172, 180–184), provides a better description of parafoveal data than both a single color channel upper envelope model (comprised of a single red-green opponent channel and an achromatic mechanism) and a vector model (combining a red-green opponent channel with an achromatic component). Thus while the two channel model ([LM] and [ML]) of foveal color vision is generalizable to the parafovea, simple models with a unitary red/green process are not. Although the two channel model can accurately fit parafoveal spectral sensitivity curves without it, a small contribution from a luminance mechanism might improve the ability of the two channel model to account for threshold discrimination and additivity data

Comparison of Panel D-15 Tests in a Large Older Population

PurposeTo determine the frequency and type of color vision defects in a large group of randomly selected older people using two versions of the D-15 and to examine the agreement between the two tests.MethodsThe Adams desaturated D-15 test was administered under Illuminant C (MacBeth lamp, ∼ 100 lux) to a group of 865 individuals aged 58 to 102 years (mean, 75.2 ± 9.1 years). No exclusion criteria, other than the reported presence of a congenital color defect, were applied. Testing was binocular with habitual near correction. If any error was made on this test, the Farnsworth D-15 was administered under identical conditions. On both tests, a color confusion score of 30 or higher was considered failing, and for those failing the test, color defect type (blue-yellow, red-green, or nonselective) was determined using the method of Vingrys and King-Smith (1988).ResultsThe majority (60.8%) of the people tested passed both tests. For the sample as a whole, the failure rates of the Adams desaturated D-15 and the Farnsworth D-15 were 36.2% and 20.76%, respectively. As expected, for both tests, failure rate increased markedly with age. Among those who failed both tests, 17.5% of the population, the proportion of specific agreement for red-green and blue-yellow defects was high, 88%. The vast majority of those failing either or both tests had blue-yellow defects, in agreement with previous studies.ConclusionsBlue-yellow defects were quite common among the aged, becoming increasingly prevalent with increasing age. More people failed the Adams desaturated D-15 than the Farnsworth D-15, but among those who failed, the proportion of blue-yellow defects was similar for the two tests, approximately 75%. The agreement between the two tests in identifying acquired red-green and blue-yellow errors was high

Longitudinal Increase in Anisometropia in Older Adults

PurposeAnisometropia shows an exponential increase in prevalence with increasing age based on cross-sectional studies. The purpose of this study was to evaluate longitudinal changes in anisometropia in all refractive components in older observers and to assess the influence of early cataract development.MethodsRefractive error was assessed at two time points separated by approximately 12 years in 118 older observers (aged 67.1 and 79.3 years at the two test times). Anisometropia defined as greater than or equal to 1.00 D was calculated for all refractive components. The subjects had intact ocular lenses in both eyes throughout the study. Lens evaluations were performed at the second test using the Lens Opacities Classification System III.ResultsAll refractive components approximately doubled in prevalence of anisometropia. Spherical equivalent anisometropia changed from 16.1 to 32.2%. Similar changes were found for spherical error (17 to 38.1%), primary astigmatism (7.6 to 17.8%), and oblique astigmatism (14.4 to 29.7%). Many who did not have anisometropia at the first visit subsequently developed anisometropia (e.g., 26.3% for spherical error and 22.9% for oblique cylinder). The onset of anisometropia occurred at all ages within the studied age range, with no particular preference for any one age. A small number lost anisometropia over time. Individual comparisons of refractive error changes in the two eyes in combination with nuclear lens changes showed that early changes in nuclear sclerosis in the two eyes could account for a large proportion of anisometropia (~40%), but unequal hyperopic shift in the spherical component in the two eyes was the primary cause of the anisometropia.ConclusionsAnisometropia is at least 10 times more common in the elderly than in children, and anisometropia develops in all refractive components in the oldest observers. Clinicians need to be aware of this common condition that could lead to binocular vision problems and potentially cause falls in the elderly

Acquired Color Vision Defects and Hexane Exposure: A Study of San Francisco Bay Area Automotive Mechanics

Occupational exposure to solvents, including n-hexane, has been associated with acquired color vision defects. Blue-yellow defects are most common and may be due to neurotoxicity or retinal damage. Acetone may potentiate the neurotoxicity of n-hexane. We present results on nonhexane solvent and hexane exposure and color vision from a cross-sectional study of 835 automotive repair workers in the San Francisco Bay Area, California (2007-2013). Cumulative exposure was estimated from self-reported work history, and color vision was assessed using the Lanthony desaturated D-15 panel test. Log-binomial regression was used to estimate prevalence ratios for color vision defects. Acquired color vision defects were present in 29% of participants, of which 70% were blue-yellow. Elevated prevalence ratios were found for nonhexane solvent exposure, with a maximum of 1.31 (95% confidence interval (CI): 0.86, 2.00) for blue-yellow. Among participants aged ≤50 years, the prevalence ratio for blue-yellow defects was 2.17 (95% CI: 1.03, 4.56) in the highest quartile of nonhexane solvent exposure and 1.62 (95% CI: 0.97, 2.72) in the highest category of exposure to hexane with acetone coexposure. Cumulative exposures to hexane and nonhexane solvents in the highest exposure categories were associated with elevated prevalence ratios for color vision defects in younger participants