Literature DB >> 12824267

Deficits in temporal integration for contrast processing in retinitis pigmentosa.

Kenneth R Alexander1, Claire S Barnes, Gerald A Fishman.   

Abstract

PURPOSE: The purpose of this study was to evaluate the properties of foveal temporal integration in patients with retinitis pigmentosa (RP) within the framework of contrast processing by the magnocellular (MC) and parvocellular (PC) pathways.
METHODS: Temporal integration functions were measured in eight patients with RP whose visual acuities ranged from 20/25 to 20/63. Contrast thresholds were obtained at durations ranging from 15 to 480 ms, using steady-pedestal and pulsed-pedestal paradigms to bias performance toward the MC and PC pathways, respectively. The patients' results were compared with those of 10 age-similar control observers with normal vision. For both paradigms, contrast thresholds as a function of duration were fit with a two-limbed function to derive the critical duration for temporal integration (t(c)) and the asymptotic threshold at long durations (Delta L(infinity)).
RESULTS: The log t(c)s of the patients with RP were significantly longer than those of the control subjects for the steady-pedestal paradigm (presumed MC-pathway mediation; t = 3.67, P < 0.001), but not for the pulsed-pedestal paradigm (presumed PC-pathway mediation; t = 0.76, P = 0.45). Further, the patients with RP showed a significant correlation between log t(c) and log Delta L(infinity) for the steady-pedestal paradigm (r = 0.72, P < 0.05) but not for the pulsed-pedestal paradigm (r = -0.37, P = 0.36).
CONCLUSIONS: The patients with RP in this study showed greater deficits in contrast sensitivity and a more prolonged critical duration under test conditions that favor the MC rather than the PC pathway. A likely explanation is a high-frequency response attenuation at the level of the cone photoreceptors that has a differential effect on contrast-processing tasks that emphasize different postreceptoral mechanisms.

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Year:  2003        PMID: 12824267     DOI: 10.1167/iovs.02-0812

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  2 in total

1.  Cell type-specific changes in retinal ganglion cell function induced by rod death and cone reorganization in rats.

Authors:  Wan-Qing Yu; Norberto M Grzywacz; Eun-Jin Lee; Greg D Field
Journal:  J Neurophysiol       Date:  2017-04-19       Impact factor: 2.714

2.  Contrast response properties of magnocellular and parvocellular pathways in retinitis pigmentosa assessed by the visual evoked potential.

Authors:  Kenneth R Alexander; Aruna S Rajagopalan; William Seiple; Vance M Zemon; Gerald A Fishman
Journal:  Invest Ophthalmol Vis Sci       Date:  2005-08       Impact factor: 4.799

  2 in total

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