September 2017
Volume 17, Issue 10
Open Access
Vision Sciences Society Annual Meeting Abstract  |   August 2017
Cortical Correlates of Aberrant Vernier Acuity in Albinism
Author Affiliations
  • Edgar DeYoe
    Radiology, Medical College of Wisconsin
  • Erica Woertz
    Cell Biology, Neurobiology & Anatomy, Medical College of Wisconsin
  • Melissa Wilk
    HudsonAlpha Institute for Biotechnology
  • Jed Mathis
    Radiology, Medical College of Wisconsin
  • Joseph Carroll
    Ophthalmology, Medical College of Wisconsin
Journal of Vision August 2017, Vol.17, 790. doi:10.1167/17.10.790
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      Edgar DeYoe, Erica Woertz, Melissa Wilk, Jed Mathis, Joseph Carroll; Cortical Correlates of Aberrant Vernier Acuity in Albinism. Journal of Vision 2017;17(10):790. doi: 10.1167/17.10.790.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Introduction: Albinism is a family of genetic diseases that cause aberrations in melanin synthesis which in turn cause aberrations in retinal development, cone density, retinocortical connectivity, and vernier acuity (VA). In healthy individuals, VA is believed to be limited by neural sampling in V1 (primary visual cortex)1. So, we asked if albinism-related deficits in VA might similarly reflect aberrations in retinocortical mapping. Methods: VA and fMRI data were obtained from 4 albinism patients (1M,3F,ages 18-31) and 4 control subjects (3M,1F,ages 20-41). VA thresholds (minimum angle of resolution, MAR) along the horizontal meridian of the left visual field were measured at 10-11 loci ranging from 0-20 degrees eccentricity using a three-dot vertical vernier stimulus. Cortical magnification (CM) was measured at 1.875x1.875x2.5 mm resolution over the same visual field range using fMRI mapping with checkered rings/wedges and a General Electric 3 Tesla MRI scanner2. Results: Overall, albinism patients had higher VA thresholds (mean foveal MAR ± SD: 5.990 ± 7.188 arcmin) than controls (0.498 ± 0.127 arcmin). MAR for controls was a power function of cortical magnification (MAR=11.15 x CM-1.192). This was also true for albinism patients, but with much more quantitative variation ranging from virtually normal (MAR = 7.68 x CM-1.373) to grossly aberrant (MAR = 107.3 x CM-1.106). Surprisingly, the two albinism patients with the most disparate VA vs CM functions had nearly identical foveal peak cone densities (46,019 vs 50,402 cones/mm2). Conclusions: Although VA varies widely across patients with albinism; it retains the quantitative relationship (power function) with CM observed in controls, albeit with wide quantitative variation. This latter variation, at least in some cases, is poorly correlated with cone densities thus emphasizing the importance of post-receptoral factors as determinants of overall visual function in albinism. 1. Duncan PMID: 12765616 2. DeYoe ISBN 978-1-4419-0345-7

Meeting abstract presented at VSS 2017

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