Investigative Ophthalmology & Visual Science Cover Image for Volume 63, Issue 7
June 2022
Volume 63, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2022
Adapting background illuminance modulates visual thresholds in patients with retinitis pigmentosa throughout the macula
Author Affiliations & Notes
  • Robert Hyde
    Illinois Eye & Ear Infirmary, Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, Illinois, United States
  • Jason Changbum Park
    Illinois Eye & Ear Infirmary, Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, Illinois, United States
  • J Jason McAnany
    Illinois Eye & Ear Infirmary, Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, Illinois, United States
  • Footnotes
    Commercial Relationships   Robert Hyde None; Jason Park None; J Jason McAnany None
  • Footnotes
    Support  P30EY001792 (UIC DOVS), K12EY021475 (RAH); unrestricted funds from Research to Prevent Blindness (UIC DOVS)
Investigative Ophthalmology & Visual Science June 2022, Vol.63, 4494 – F0281. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Robert Hyde, Jason Changbum Park, J Jason McAnany; Adapting background illuminance modulates visual thresholds in patients with retinitis pigmentosa throughout the macula. Invest. Ophthalmol. Vis. Sci. 2022;63(7):4494 – F0281.

      Download citation file:


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

      ×
  • Supplements
Abstract

Purpose : To quantify patterns of threshold elevation under different light adaptation conditions throughout the macula in patients with retinitis pigmentosa (RP).

Methods : Nine subjects with RP (24 to 59 years old) and 10 visually-normal individuals (18 to 49 years old) participated. Threshold was measured at 7 locations along the horizontal meridian of the visual field (10o nasal to 10o temporal) using Goldmann size III targets. The field locations were grouped into three regions based on eccentricity from fixation: perifoveal (5o-10o), parafoveal (2o) and foveal. Threshold was measured under DA conditions using long-wavelength stimuli and across a broad range of adaptation levels (DA to 50 cd/m2) using short-wavelength stimuli. The relationship between threshold and adaptation level across the field was described using a standard “threshold-vs-illuminance” (TvI) model to derive absolute threshold (To), slope (n), and eigengrau (Ao). Repeated measures analysis of variance (ANOVA) was used to compare the three fit parameters between the two subject groups.

Results : Under DA conditions, thresholds for the short- and long-wavelength stimuli were similar throughout the visual field for 8 of 9 subjects, consistent with the cone pathway mediating threshold at all locations. Threshold elevation was greater for the RP subjects under DA and low adaptation conditions, compared to LA conditions. ANOVA indicated significantly elevated To and Ao for the RP subjects for each field location. The value of n was approximately independent of field location for the RP subjects and increased with eccentricity for the controls. This pattern resulted in significantly increased n in the fovea and significantly decreased n in the perifovea (both p < 0.05), with no significant difference in the parafovea (p = 0.17).

Conclusions : The approximately similar elevations in To and Ao for the RP subjects suggests that reduced quantal absorption may underlie threshold elevation throughout the macula in this cohort of RP subjects. Alternatively, the results may be attributed to the lack of rod function in these RP subjects, which would elevate DA threshold more than LA threshold.

This abstract was presented at the 2022 ARVO Annual Meeting, held in Denver, CO, May 1-4, 2022, and virtually.

×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×