Kr. Alexander et al., Contrast discrimination deficits in retinitis pigmentosa are greater for stimuli that favor the magnocellular pathway, VISION RES, 41(5), 2001, pp. 671-683
Luminance contrast discrimination was measured in 14 patients with retiniti
s pigmentosa (RP) and 14 control observers with normal vision, using steady
-pedestal and pulsed-pedestal paradigms [Pokorny, J., & Smith, V. C. (1997)
. Psychophysical signatures associated with magnocellular and parvocellular
pathway contrast gain. Journal of the Optical Society of America A, 14, 24
77-2486] to bias performance toward the magnocellular (MC) or parvocellular
(PC) pathway, respectively. The aim was to determine the relative effects
of retinal degeneration on MC- and PC-pathway function in RP. For five of t
he RP patients, contrast discrimination thresholds were within normal limit
s for both the steady-pedestal and pulsed-pedestal paradigms. The other nin
e RP patients showed threshold elevations for the steady-pedestal paradigm
(presumed magnocellular mediation), whereas their thresholds for the pursed
-pedestal paradigm (presumed parvocellular mediation) were within normal li
mits for all but the two patients who had the most extreme threshold elevat
ions using the steady-pedestal paradigm. A control experiment on four of th
e RP patients, using a greater number of pedestal contrasts, verified that
the patients' thresholds for the pulsed-pedestal paradigm showed the patter
n expected for contrast discrimination mediated by the PC pathway. The high
er threshold elevations for the steady-pedestal paradigm than for the pulse
d-pedestal paradigm indicate that the retinal degeneration that occurs in R
P predominantly disrupts contrast discrimination under stimulus conditions
that favor the MC pathway. (C) 2001 Elsevier Science Ltd. All rights reserv
ed.