Pseudorandom full-field electroretinograms reflect different light adaptation mechanisms.

PURPOSE: To investigate the magnitude and time course of pseudorandom ffERG during light adaptation. METHODS: Ten healthy subjects (26 ± 10.1 years) underwent 20 min of dark adaptation, and then the ffERG was evoked by pseudorandom flash sequences (4 ms per flash, 3 cd.s/m2) driven by m-sequences (210-1 stimulus steps) using Veris Science software and a Ganzfeld dome over a constant field of light adaptation (30 cd/m2). The base period of the m-sequence was 50 ms. Each stimulation sequence lasting 40 s was repeated at 0, 5, 10, 15 and 20 min of light adaptation. Relative amplitude and latency (corrected by values found at 0 min) of the three components (N1, P1, and N2) of first-order (K1) and first slice of the second-order (K2.1) kernel at 5 time points were evaluated. An exponential model was fitted to the mean amplitude and latency data as a function of the light adaptation duration to estimate the time course (τ) of the light adaptation for each component. Repeated one-way ANOVA followed by Tukey post-test was applied to the amplitude and latency data, considering significant values of p < 0.05. RESULTS: Regarding the K1 ffERG, N1 K1, P1 K1, and N2 K1 presented an amplitude increase as a function of the light adaptation (N1 K1 τ value = 2.66 min ± 4.2; P1 K1 τ value = 2.69 min ± 2.10; and N2 K1 τ value = 3.49 min ± 2.96). P1 K1 and N2 K1 implicit time changed as a function of the light adaptation duration (P1 K1 τ value = 3.61 min ± 5.2; N2 K1 τ value = 3.25 min ± 4.8). N1 K1 had small implicit time changes during the light adaptation. All the K2,1 components also had nonsignificant changes in amplitude and implicit time during the light adaptation. CONCLUSIONS: Pseudorandom ffERGs showed different mechanisms of adaptation to retinal light. Our results suggest that K1 ffERG is generated by retinal mechanisms with intermediate- to long-term light adaptation, while K2.1 ffERG is generated by retinal mechanism with fast light adaptation course.

Early visual changes in diabetic patients with no retinopathy measured by color discrimination and electroretinography

Early visual changes caused by diabetes include color vision losses and an abnormal full-field electroretinogram. The purpose of this study was to evaluate color vision in type 2 diabetic patients with no clinically detectable retinopathy using an objective psychophysical color vision test, evaluate retinal function assessed by full-field electroretinography (ffERG), and verify the agreement among the changes detected by each of these tests. Color vision was tested and ffERG was performed in 34 diabetic patients (20 males; ages 56 ± 9 years). Results were compared with those obtained from age-matched control groups. Color discrimination losses occurred in all three color-confusion axes with a higher incidence on the protan axis. The full-field electroretinographic data indicated that inner retinal components (i.e., ffERG oscillatory potentials) were more affected than outer retinal components, indicating impairment of second- and third-order retinal neurons early in the disease. Previous studies reported tritan losses as a classic color vision defect in diabetes, but our results showed that all three color-confusion axes (i.e., protan, deutan, and tritan) are compromised, at least during the very early stages of the disease, reflecting a diffuse pattern of color vision loss. The full-field electroretinographic results that showed abnormalities of the inner retina support the color vision findings...

Early visual changes in diabetic patients with no retinopathy measured by color discrimination and electroretinography

Early visual changes caused by diabetes include color vision losses and an abnormal full-field electroretinogram. The purpose of this study was to evaluate color vision in type 2 diabetic patients with no clinically detectable retinopathy using an objective psychophysical color vision test, evaluate retinal function assessed by full-field electroretinography (ffERG), and verify the agreement among the changes detected by each of these tests. Color vision was tested and ffERG was performed in 34 diabetic patients (20 males; ages 56 ± 9 years). Results were compared with those obtained from age-matched control groups. Color discrimination losses occurred in all three color-confusion axes with a higher incidence on the protan axis. The full-field electroretinographic data indicated that inner retinal components (i.e., ffERG oscillatory potentials) were more affected than outer retinal components, indicating impairment of second- and third-order retinal neurons early in the disease. Previous studies reported tritan losses as a classic color vision defect in diabetes, but our results showed that all three color-confusion axes (i.e., protan, deutan, and tritan) are compromised, at least during the very early stages of the disease, reflecting a diffuse pattern of color vision loss. The full-field electroretinographic results that showed abnormalities of the inner retina support the color vision findings.(AU)

Comparison of the reliability of multifocal visual evoked cortical potentials generated by pattern reversal and pattern pulse stimulation

This study compared the effectiveness of the multifocal visual evoked cortical potentials (mfVEP) elicited by pattern pulse stimulation with that of pattern reversal in producing reliable responses (signal-to-noise ratio >1.359). Participants were 14 healthy subjects. Visual stimulation was obtained using a 60-sector dartboard display consisting of 6 concentric rings presented in either pulse or reversal mode. Each sector, consisting of 16 checks at 99% Michelson contrast and 80 cd/m² mean luminance, was controlled by a binary m-sequence in the time domain. The signal-to-noise ratio was generally larger in the pattern reversal than in the pattern pulse mode. The number of reliable responses was similar in the central sectors for the two stimulation modes. At the periphery, pattern reversal showed a larger number of reliable responses. Pattern pulse stimuli performed similarly to pattern reversal stimuli to generate reliable waveforms in R1 and R2. The advantage of using both protocols to study mfVEP responses is their complementarity: in some patients, reliable waveforms in specific sectors may be obtained with only one of the two methods. The joint analysis of pattern reversal and pattern pulse stimuli increased the rate of reliability for central sectors by 7.14% in R1, 5.35% in R2, 4.76% in R3, 3.57% in R4, 2.97% in R5, and 1.78% in R6. From R1 to R4 the reliability to generate mfVEPs was above 70% when using both protocols. Thus, for a very high reliability and thorough examination of visual performance, it is recommended to use both stimulation protocols.

Investigação eletrofisiológica multifocal de sujeitos com toxoplasmose ocular / Multifocal eletctrophysiological investigation of subjects with ocular toxoplasmosis

Objetivo: avaliar as amplitudes das respostas eletrorretinográficas multifocais de pacientes com perda visual decorrentes de toxoplasmose ocular. Método: estudo longitudinal prospectivo comparativa no qual foi usado o sistema VERIS Science v6.0.5d para estimulação, registro e extração da resposta para cada hexágono que constitui o estímulo em 3 sujeitos com toxoplasmose ocular (grupo estudo) e 10 sujeitos saudáveis (grupo controle). Os dados dos registros foram exportados para análise no ambiente de programação MATLAB. Neste ambiente de programação foi realizada a análise dos componentes principais sobre as respostas multifocais para aumentar a razão sinal-ruído dos registros. A amplitude do registro dos pacientes foi comparada com os resultados do grupo controle. Foi realizada a avaliação psicofísica do campo visual em todos os indivíduos através da perimetria estática de Humphrey. Resultados: os registros de todos os sujeitos saudáveis exibiram três deflexões como descritos internacionalmente. Nos pacientes com toxoplasmose ocular os resultados da amplitude de resposta apresentaram semelhanças dos obtidos com a perimetria visual. Conclusão: a eletrorretinografia multifocal permite quantificar as perdas de sensibilidade retiniana em pacientes com toxoplasmose ocular de uma forma que pode ser diretamente comparável à avaliação psicofísica do campo visual.

Purpose: to perform a quantitative analysis of the visual losses of three patients suffering from ocular toxoplasmosis by using multifocal electroretinography. Methods: a VERIS Science v6.0.5d hardware and software was used to evoke retinal bioelectric activity, to record this activity, and to extract its first order kernel. Data were exported to MATLAB environment to perform a principal component analysis of the first order kernel. Multifocal eletroretinography obtained from patients were then compared with those obtained from healthy subjects. We performed psychophysical assessment of visual in all subjects through the static Humphrey perimetry Results: recordings from healthy subjects exhibited three components. Ocular toxoplasmosis patients had decreased response amplitude in many areas of the retina and the pattern of visual loss is similar to that found by threshold static automated perimetry. Conclusion: patients with ocular toxoplasmosis showed different degrees of visual impairment that were revealed by using multifocal electrorretinography. The electrophysiological losses matched those revealed by threshold static automated perimetry.