The field topography of evoked potentials is the dependent of the responses on the location of a small stimulus in the visual field. Field topographies are derived with a method of simultaneous stimulation of a large number of locations and extraction of the local responses from a single response signal. The techniques for such studies have been developed and tested. Goal 1: Determination of the field topography of the luminance and pattern ERGs and their components. Correlation of these topographies with densities of retinal receptors and ganglion cells. Inter-subject differences will be studied to establish a baseline for a clinical evaluation. Goal 2: Development of an objective test of local retinal function for the purpose of screening, diagnosis and monitoring of patients. The field plots will be derived from patients with specific etiologies (glaucoma, ocular hypertension, maculopathy). The plots will be compared with fundus images to establish the exact location of retinal areas with abnormal ERG responses. ERG fields will be compared with psychophysical fields to assess their sensitivity in the detection of local pathological changes. Goal 3: Identification and characterization of ERG components from different retinal layers. This will be achieved with different modes of pattern stimulation and techniques of nonlinear systems analysis. Goal 4: Identification of VEP components from different visual areas of cortex. Functional characterization of their sources on the basis of nonlinear systems analysis. The field topography of the VEP is very complex due to the convoluted cortical anatomy. For each stimulus location, the relative contributions to the response from various cortical sources are different. A principal component analysis (SVD) will be applied to the responses at locations of comparable eccentricity in the visual field, to determine the subspace spanned by the components from different sources. The kernel structure of the nonlinear responses will be used to identify and characterize the components within this subspace. The invariance of the components between subjects will be tested to confirm the decomposition.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY006861-06
Application #
3263552
Study Section
Visual Sciences B Study Section (VISB)
Project Start
1986-05-01
Project End
1994-03-31
Budget Start
1992-04-01
Budget End
1994-03-31
Support Year
6
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Smith-Kettlewell Eye Research Institute
Department
Type
DUNS #
City
San Francisco
State
CA
Country
United States
Zip Code
94115
Gerth, Christina; Sutter, Erich E; Werner, John S (2003) mfERG response dynamics of the aging retina. Invest Ophthalmol Vis Sci 44:4443-50
Poloschek, Charlotte M; Sutter, Erich E (2002) The fine structure of multifocal ERG topographies. J Vis 2:577-87
Shimada, Y; Li, Y; Bearse Jr, M A et al. (2001) Assessment of early retinal changes in diabetes using a new multifocal ERG protocol. Br J Ophthalmol 85:414-9
Hood, D C; Bearse Jr, M A; Sutter, E E et al. (2001) The optic nerve head component of the monkey's (Macaca mulatta) multifocal electroretinogram (mERG). Vision Res 41:2029-41
Palmowski, A M; Sutter, E E; Bearse Jr, M A et al. (1999) Das multifokale elektroretinogramm in der diagnostik und verlaufskontrolle lokalisierter Netzhautfunktionsstorungen: fallbericht eines patienten mit chorioretinopathia centralis serosa. Ophthalmologica 213:327-35
Baseler, H A; Sutter, E E; Klein, S A et al. (1994) The topography of visual evoked response properties across the visual field. Electroencephalogr Clin Neurophysiol 90:65-81
Sutter, E E; Tran, D (1992) The field topography of ERG components in man--I. The photopic luminance response. Vision Res 32:433-46
Sutter, E E; Vaegan (1990) Lateral interaction component and local luminance nonlinearities in the human pattern reversal ERG. Vision Res 30:659-71