Contrast Sensitivity Mediated by Inferred Magno- and Parvocellular Pathways in Type 2 Diabetics with and without Nonproliferative Retinopathy


Autoria(s): GUALTIERI, Mirella; BANDEIRA, Marcio; HAMER, Russell David; DAMICO, Francisco Max; MOURA, Ana Laura Araujo; VENTURA, Dora Fix
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

Resumo

PURPOSE. To evaluate achromatic contrast sensitivity (CS) with magnocellular-(M) and parvocellular-(P) probing stimuli in type 2 diabetics, with (DR) or without (NDR) nonproliferative retinopathy. METHODS. Inferred M-and P-dominated responses were assessed with a modified version of the steady-/pulsed-pedestal paradigm (SP/PP) applied in 26 NDR (11 male; mean age, 55 +/- 9 years; disease duration, 5 +/- 4 years); 19 DR (6 male; mean age, 58 +/- 7 years; disease duration = 9 +/- 6 years); and 18 controls (CTRL; 12 male; mean age, 55 +/- 10 years). Thresholds were measured with pedestals at 7, 12, and 19 cd/m(2), and increment durations of 17 and 133 ms. The thresholds from the two stimulus durations were used to estimate critical durations (Tc) for each data set. RESULTS. Both DR and NDR patients had significant reduction in CS in both SP and PP paradigms in relation to CTRL (Kruskal-Wallis, P < 0.01). Patients` critical duration estimates for either paradigm were not significantly different from CTRL. CONCLUSIONS. The significant reduction of CS in both paradigms is consistent with losses of CS in both M and P pathways. The CS losses were not accompanied by losses in temporal processing speed in either diabetic group. Significant CS loss in the group without retinopathy reinforces the notion that neural changes associated with the cellular and functional visual loss may play an important role in the etiology of diabetic visual impairment. In addition, the results show that the SP/PP paradigm provides an additional tool for detection and characterization of the early functional damage due to diabetes. (Invest Ophthalmol Vis Sci. 2011; 52:1151-1155) DOI:10.1167/iovs.09-3705

FAPESP (Fundacao de Amparo a Pesquisa do Estado de Sao Paulo)[02/12733-8]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP (Fundacao de Amparo a Pesquisa do Estado de Sao Paulo)[04/15926-7]

Identificador

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, v.52, n.2, p.1151-1155, 2011

0146-0404

http://producao.usp.br/handle/BDPI/32183

10.1167/iovs.09-3705

http://dx.doi.org/10.1167/iovs.09-3705

Idioma(s)

eng

Publicador

ASSOC RESEARCH VISION OPHTHALMOLOGY INC

Relação

Investigative Ophthalmology & Visual Science

Direitos

restrictedAccess

Copyright ASSOC RESEARCH VISION OPHTHALMOLOGY INC

Palavras-Chave #RETINAL GANGLION-CELLS #VISUAL FUNCTION #PRIMATE RETINA #VISION #EYE #ABNORMALITIES #THRESHOLDS #LUMINANCE #DEFICITS #DISEASE #Ophthalmology
Tipo

article

original article

publishedVersion