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Dive into the research topics where Gary L. Trick is active.

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Featured researches published by Gary L. Trick.


Neurology | 1991

Visual sensitivity to motion: Age‐related changes and deficits in senile dementia of the Alzheimer type

Gary L. Trick; Scott E. Silverman

To determine whether motion sensitivity varies with age, we measured motion discrimination in visual normals 25 to 80 years of age and found that motion thresholds increased linearly with age and were approximately two times higher in those 70 to 80 years old than in participants under thirty. This increase was not attributable to pupil size or retinal image distortion, but probably reflects neurodegeneration in the primary visual pathway. We compared the motion sensitivity of patients with senile dementia of the Alzheimer type (SDAT) with results from a subset of the visual normals of similar age. In SDAT patients, there were significant threshold elevations, which were more pronounced in the patients with more severe dementia. These findings confirm previous reports of visual system involvement in SDAT and indicate motion testing may reveal preclinical visual system involvement in SDAT.


Ophthalmology | 1989

Assessing the Utility of Reliability Indices for Automated Visual Fields: Testing Ocular Hypertensives

Michelle Bickler-Bluth; Gary L. Trick; Allan E. Kolker; Dorothy G. Cooper

Monocular (right eye) visual fields were recorded with the Humphrey Visual Field Analyzer (30-2 Program) at baseline as well as 6 and 12 months later in 120 patients with established ocular hypertension. Indices of field reliability (fixation loss, less than 20%; false-positives and false-negatives, less than 33%) and field sensitivity (mean deviation [MD] and pattern standard deviation [PSD]) were examined. At baseline, 35% of patients exhibited low reliability (LR) fields, a figure which decreased to approximately 25% at 6 and 12 months, respectively. During this period, over 50% of patients produced at least one LR field, whereas 8.3% were unable to produce even one reliable field. Exhibition of a LR field appeared to be independent of patient age. Fixation errors, the major cause of LR fields, decreased by approximately 10% over the 12-month period; most patients had between 20 and 32% fixation errors. The incidence of significant defects identified by PSD was greater than that for MD; this was true for both reliable and LR fields. It is suggested that increasing the fixation loss criteria for assessing patient reliability to a 33% cutoff might substantially increase the percentage of fields graded reliable with minimal effect on the sensitivity or specificity of the test.


Documenta Ophthalmologica | 1991

The pattern electroretinogram in retinal and optic nerve disease : a quantitative comparison of the pattern of visual dysfunction

Ronit Nesher; Gary L. Trick

A retrospective analysis was performed on the transient and steady-state pattern electroretinograms recorded from 42 patients with glaucoma, 13 patients with senile dementia of the Alzheimers type, 58 patients with diabetes mellitus, and 92 control subjects to evaluate the pattern of electroretinographic changes associated with retinal and optic nerve disease. The amplitudes of both the initial positive component (N1 to P1) and the subsequent negative component (P1 to N2) of the transient (4 rps) responses were measured. From these measurements the (P1 to N2)/(N1 to P1) was derived. The N1 to P1 amplitude of the steady-state pattern electroretinogram also was measured. In the glaucoma patients all three amplitude measures, as well as the amplitude ratio of the components of the transient response, were reduced significantly compared with age-matched controls (p < 0.05). A similar pattern was detected in the patients with Alzheimers disease, but in this case the only statistically significant amplitude reduction was in the steady-state pattern electroretinogram. A different pattern was observed among the diabetic patients (both with and without retinopathy). Only minor reductions in the amplitude of the transient pattern electroretinogram, which were not statistically significant, were noted. In addition, the ratio of the amplitudes of the components of the transient response did not differ from age-matched controls. The amplitude of the steady-state pattern electroretinogram was reduced in diabetics, but this was significant only for those patients with retinopathy (p < 0.01). These findings support the suggestion that an analysis of both the positive and negative components of the pattern electroretinogram may be useful for differentiating the contributions of retinal and optic nerve dysfunction to visual impairment. The results also indicate that in both retinal and optic nerve disease the steady-state pattern electroretinogram can be an earlier sign of dysfunction than the transient pattern electroretinogram.


Documenta Ophthalmologica | 1987

Pattern reversal retinal potentials in ocular hypertensives at high and low risk of developing glaucoma.

Gary L. Trick

The human pattern-reversal retinal potential (PRRP) is a bioelectrical response which reflects neural activity generated in the proximal retina. Visual diseases which affect the retinal ganglion cells and the optic nerve often produce significant reductions in the amplitude of the PRRP. PRRP amplitude reductions are frequently observed in patients with primary open-angle glaucoma. This investigation was designed to determine whether patients with ocular hypertension who are at risk of developing glaucoma also exhibit PRRP amplitude reductions. The results indicate that PRRP amplitude reductions do occur in some ocular hyptertensives, but many other ocular hypertensives do not exhibit PRRP abnormalities.


Current Eye Research | 1988

Pattern reversal electroretinogram (PRERG) abnormalities in ocular hypertension: correlation with glaucoma risk factors

Gary L. Trick; Michelle Bickler-Bluth; Dorothy G. Cooper; Allan E. Kolker; Ronit Nesher

The indices employed commonly for the diagnosis of glaucoma (tonometry, ophthalmoscopy and perimetry) do not always identify which patients with ocular hypertension (OHT) will develop primary open-angle glaucoma (POAG) before irreversible visual field loss is manifest (1). The human pattern reversal electroretinogram (PRERG) is a bioelectric response reflecting neural activity of the proximal retina. PRERG amplitude reductions have been observed in POAG and other diseases affecting the optic nerve and retinal ganglion cells. This study was designed to determine whether OHT patients exhibit PRERG amplitude reductions and whether PRERG results are correlated with routinely evaluated clinical parameters. Steady-state PRERG (16 rps) were elicited by high contrast (76%), phase alternating checkerboard patterns (15-20 min checks) from one eye of 130 patients with ocular hypertension and 47 age matched visual normals (AMVNs). A significant (p less than 0.05) reduction in PRERG amplitude was noted for the OHT patients and 11.5% of those patients exhibited PRERG amplitudes more than 2.0 standard deviations below the AMVN mean. PRERG amplitude was found to be positively correlated with diastolic blood pressure (DBP) and negatively correlated with age, but no correlation between PRERG amplitude and either IOP, C/D ratio, or systolic blood pressure was evident. The lack of correlation between PRERG amplitude and the commonly used clinical indices may suggest a complementary role for this neurophysiologic test in determining which OHT patients will develop glaucoma.


Documenta Ophthalmologica | 1990

Steady-state pattern electroretinogram following long term unilateral administration of timolol to ocular hypertensive subjects*

Ronit Nesher; Gary L. Trick; Michael A. Kass; Mae O. Gordon

To determine whether long-term reduction of intraocular pressure leads to a corresponding preservation of the pattern electroretinogram (PERG), PERGs were studied in 21 patients with ocular hypertension who had received unilateral timolol therapy for a minimum of 6 years. The mean difference in intraocular pressure (IOP) between the placebotreated and the timolol-treated eyes (over 6 years) was 2.4mm Hg. Steady-state PERGs (16.0 rps) were obtained simultaneously in both eyes of each patient, with four check sizes (0.25, 0.5, 1.0 and 2.0 degrees). Significant (p < 0.05) steady-state PERG deficits (i.e., amplitude more than two standard deviations below the mean value of age-matched controls) were observed in 16 eyes of 12 patients (10 placebo-treated and 6 timolol-treated eyes). The mean PERG amplitude did not differ significantly between the placebo-treated and timololtreated eyes. However, a significant correlation (r = - 0.423) in the IOP differences between the placebo-treated and timolol-treated eyes and the corresponding PERG amplitude differences was noted in three of the four test conditions (i.e. 0.25, 0.5, and 1.0 degrees). These results suggest that reducing IOP may preserve ganglion cell function in some patients with ocular hypertension.


Annals of Neurology | 1989

Abnormal pattern electroretinograms in patients with senile dementia of the alzheimer type

Gary L. Trick; Michael C. Barris; Michelle Bickler-Bluth


Ophthalmology | 1988

The Relationship between Hue Discrimination and Contrast Sensitivity Deficits in Patients with Diabetes Mellitus

Gary L. Trick; Ronald M. Burde; Mae O. Cordon; Julio V. Santiago; Charles Kilo


Ophthalmology | 1990

Visual Field Defects in Patients with Insulin-dependent and Noninsulin-dependent Diabetes

Gary L. Trick; Linda R. Trick; Charles Kilo


Documenta Ophthalmologica | 1988

Retinocortical conduction time in diabetics with abnormal pattern reversal electroretinograms and visual evoked potentials

Gary L. Trick; Ronald M. Burde; Mae O. Gordon; Charles Kilo; Julio V. Santiago

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Charles Kilo

Washington University in St. Louis

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Michelle Bickler-Bluth

Washington University in St. Louis

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Ronit Nesher

Washington University in St. Louis

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Allan E. Kolker

Washington University in St. Louis

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Dorothy G. Cooper

Washington University in St. Louis

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Julio V. Santiago

Washington University in St. Louis

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Linda R. Trick

University of Missouri–St. Louis

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Mae O. Gordon

Washington University in St. Louis

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Ronald M. Burde

Albert Einstein College of Medicine

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Kathleen M. Haywood

University of Missouri–St. Louis

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