May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Color Space Distortions in Patients With Type 2 Diabetes Mellitus
Author Affiliations & Notes
  • C. Feitosa–Santana
    University of Sao Paulo, Sao Paulo, Brazil
    Psicologia Experimental,
  • G.V. Paramei
    Hanse Institute for Advanced Study, Delmenhorst, Germany
  • N.N. Oiwa
    University of Sao Paulo, Sao Paulo, Brazil
    Fisica Geral,
  • D. Bimler
    Department of Health and Human Development, Massey University, Palmerston North, New Zealand
  • M.F. Costa
    University of Sao Paulo, Sao Paulo, Brazil
    Psicologia Experimental,
  • M. Lago
    University of Sao Paulo, Sao Paulo, Brazil
    Psicologia Experimental,
  • M. Nishi
    University of Sao Paulo, Sao Paulo, Brazil
    Hospital Universitário,
  • D.F. Ventura
    University of Sao Paulo, Sao Paulo, Brazil
    Psicologia Experimental,
  • Footnotes
    Commercial Relationships  C. Feitosa–Santana, None; G.V. Paramei, None; N.N. Oiwa, None; D. Bimler, None; M.F. Costa, None; M. Lago, None; M. Nishi, None; D.F. Ventura, None.
  • Footnotes
    Support  Temático FAPESP, CNPq, CAPES–PROCAD; DFV is a CNPq research fellow and CFS has a FAPESP MA fellowship
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 3699. doi:
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      C. Feitosa–Santana, G.V. Paramei, N.N. Oiwa, D. Bimler, M.F. Costa, M. Lago, M. Nishi, D.F. Ventura; Color Space Distortions in Patients With Type 2 Diabetes Mellitus . Invest. Ophthalmol. Vis. Sci. 2006;47(13):3699.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : To compare psychophysical color vision spaces calculated from data on similarity judgements made by nonretinopathic diabetes mellitus type 2 (DM2) patients and controls.

Methods: : DM2 patients (n=32) and age–matched controls (n=23) were tested monocularly in both eyes; all underwent an ophthalmological examination. Color vision was assessed with the Farnsworth D–15 test, to screen for congenital deficiencies, and with the Lanthony D–15d test. For their color space estimation, subsets of caps from both tests were employed in a triadic procedure. Based on each subject’s ‘odd–one–out’ choices, subjective dissimilarities between the caps were computed and processed with multidimensional scaling. Two–dimensional color spaces were reconstructed for individuals and groups. Dimensions were interpreted as the R/G and B/Y perceptual opponent systems.

Results: : Lanthony D–15d scores of patients were not significantly different from controls (TCDS for controls: 60.25 ± 5.84 OO; for DM2 patients: 66.04 ± 13.61, OD, and 67.29 ± 17.32, OS). Color spaces of DM2 patients, compared to controls, were compressed along the B/Y and R/G dimensions: residuals (average square difference) for right eye (OD) and left eye (OS) along the B/Y dimension were: OD = 0.17 and OS = 0.26; along the R/G dimension were: OD = 0.15 and OS = 0.21. However, the degree of the space compression varied dramatically among individual patients.

Conclusions: : The present findings are in agreement with earlier studies demonstrating diffuse losses in early stages of DM2. The proposed method of testing, which includes caps varying in saturation and lightness, and uses color spaces to represent discrimination, provides an opportunity for more differentiated, quantitative diagnosis of the type (the perceptual color system affected) and the severity of color vision loss.

Keywords: perception • neuro-ophthalmology: diagnosis • retinopathy of prematurity 
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