April 2011
Volume 52, Issue 14
Free
ARVO Annual Meeting Abstract  |   April 2011
Beta-Zone Parapapillary Atrophy (ßPPA) and Multifocal Visual Evoked Potentials (mfVEP) in Eyes with Glaucomatous Optic Neuropathy (GON)
Author Affiliations & Notes
  • Scott Ketner, Jr.
    Einhorn Clinical Research Center, New York Eye and Ear Infirmary, New York, New York
    Bronx-Lebanon Hospital Center, Bronx, New York
  • Carlos Gustavo De Moraes
    Einhorn Clinical Research Center, New York Eye and Ear Infirmary, New York, New York
    New York University School of Medicine, New York, New York
  • Christopher C. Teng
    Einhorn Clinical Research Center, New York Eye and Ear Infirmary, New York, New York
  • Joshua R. Ehrlich
    Weill Cornell Medical College, New York, New York
  • Ali S. Raza
    Columbia University, New York, New York
  • Jeffrey M. Liebmann
    Einhorn Clinical Research Center, New York Eye and Ear Infirmary, New York, New York
    New York University School of Medicine, New York, New York
  • Robert Ritch
    Einhorn Clinical Research Center, New York Eye and Ear Infirmary, New York, New York
  • Donald C. Hood
    Columbia University, New York, New York
  • Footnotes
    Commercial Relationships  Scott Ketner, Jr., None; Carlos Gustavo De Moraes, None; Christopher C. Teng, None; Joshua R. Ehrlich, None; Ali S. Raza, None; Jeffrey M. Liebmann, None; Robert Ritch, None; Donald C. Hood, None
  • Footnotes
    Support  Pamela Bennett Research Fund of the New York Glaucoma Research Institute, New York, NY; and NIH grant EY02115
Investigative Ophthalmology & Visual Science April 2011, Vol.52, 5489. doi:
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      Scott Ketner, Jr., Carlos Gustavo De Moraes, Christopher C. Teng, Joshua R. Ehrlich, Ali S. Raza, Jeffrey M. Liebmann, Robert Ritch, Donald C. Hood; Beta-Zone Parapapillary Atrophy (ßPPA) and Multifocal Visual Evoked Potentials (mfVEP) in Eyes with Glaucomatous Optic Neuropathy (GON). Invest. Ophthalmol. Vis. Sci. 2011;52(14):5489.

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

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Abstract

Purpose: : To investigate changes in mfVEP responses due to ßPPA.

Methods: : Patients with GON with or without standard achromatic perimetry (SAP) abnormalities were referred for mfVEP testing during a 2-year period. Eyes with good quality optic disc stereophotographs and reliable SAP results within 12 months of the mfVEP test were included. Photographs were reviewed by 2 glaucoma specialists and classified based on the presence of ßPPA. Disagreement was adjudicated by a third specialist. Monocular mean latency delays (ms) and amplitudes (SNR) were compared between groups. Age, SAP mean deviation (MD), pattern standard deviation (PSD), and spherical equivalent (SE) were analyzed in the multivariate model. Nested ANOVA and generalized estimated equations were used for comparisons between groups after adjusting for inter-eye associations.

Results: : Of the 394 eyes (200 patients), 223 (57%) eyes had ßPPA based on review of photographs. The ßPPA eyes were older (59.6±13.7 vs 56.5±13.7 yr, p=0.02), more myopic (-4.0±3.5 vs -1.3±3.5 D, p<0.01), and had worse SAP (MD: -4.9±5.2 vs -2.6±5.2 dB, p<0.01; PSD: 4.3±2.9 vs 2.5±3.0 dB, p<0.01). By univariate analysis, mean latencies were longer in ßPPA eyes (6.1±5.3 vs 4.0±5.5 ms, p<0.01). By multivariate analysis, after adjusting for differences in SE, age, and SAP MD, there was no significant difference between the two groups (p=0.09). βPPA width in clock-hours significantly correlated with SAP severity and mfVEP latency, even after adjusting for age and SE. ßPPA eyes had lower amplitude log SNR (0.49±0.16 vs. 0.56±0.15, p<0.01), which lost significance (p=0.51) after adjusting for MD and PSD.

Conclusions: : Although eyes with ßPPA had significantly lower amplitudes and prolonged latencies than eyes without ßPPA, these differences were attributable to differences in SAP severity, age, and refractive error. Thus, ßPPA does not appear to be an independent factor affecting mfVEP responses in eyes with GON.

Keywords: electrophysiology: clinical • optic disc • visual fields 
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