Ma. Sandberg et al., THE RELATIONSHIP BETWEEN VISUAL-FIELD SIZE AND ELECTRORETINOGRAM AMPLITUDE IN RETINITIS-PIGMENTOSA, Investigative ophthalmology & visual science, 37(8), 1996, pp. 1693-1698
Purpose. To determine to what degree visual held size is correlated wi
th electroretinogram (ERG) amplitude among patients with the common fo
rms of retinitis pigmentosa (RP). Methods. Visual field equivalent dia
meter to the V4e white test light of the Goldmann perimeter was correl
ated with log ERG amplitude elicited by 0.5 Hz or 30 Hz full-field fla
shes of white light. Primary analyses were conducted on data from 583
patients with the common forms of RP. Subset analyses were performed o
n data from patients with ERG responses with different ranges of ampli
tude to assess to what extent the correlation depends on ERG amplitude
, as well as on data from patients of a given genetic type to determin
e whether the correlation depends on the mode of transmission. Data fr
om patients with the rhodopsin, Pro23His mutation (n = 38) or with the
rhodopsin, Pro347Leu mutation (n = 24) were analyzed to determine the
correlation between visual field size and ERG amplitude for patients
with the same mutation. Results, Visual field size was significantly c
orrelated with ERG amplitude for every comparison (P less than or equa
l to 0.0003). Correlations generally were higher for ERGs elicited by
30 Hz flashes (r = 0.62 for the entire sample) than they were for thos
e elicited by 0.5 Hz flashes (r = 0.53 for the entire sample). They we
re lower for truncated ranges of ERG amplitude, higher for patients wi
th dominant or recessive disease than for patients with x-linked disea
se or for patients of all genetic types combined, and strong for patie
nts with the same rhodopsin mutation (reaching a value of 0.87). Concl
usions, Visual field size is significantly correlated with ERG amplitu
de for patients with RP. Correlation depends on the range of ERG ampli
tudes, the inheritance type, and, particularly, on whether the analysi
s is confined to a single gene mutation.