July 2018
Volume 59, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2018
Changes in Macular function with Multifocal Pupillography and its spatial correlation with severity of Diabetic Retinopathy
Author Affiliations & Notes
  • Faran Sabeti
    Department of Optometry, University of Canberra, Bruce, Australian Capital Territory, Australia
    Eccles Institute for Neuroscience, Australian National University, Canberra, Australian Capital Territory, Australia
  • Corinne F Carle
    Eccles Institute for Neuroscience, Australian National University, Canberra, Australian Capital Territory, Australia
  • Christopher Nolan
    Australian National University Medical School, Australian National University, Canberra, Australian Capital Territory, Australia
    Department of Endocrinology, The Canberra Hospital, Canberra, Australian Capital Territory, Australia
  • Alicia Jenkins
    NHMRC Clinical Trials Centre, University of Sydney, Sydney, Australian Capital Territory, Australia
  • Rohan Essex
    Australian National University Medical School, Australian National University, Canberra, Australian Capital Territory, Australia
    Department of Ophthalmology, The Canberra Hospital, Canberra, Australian Capital Territory, Australia
  • Lauren Baker
    Department of Endocrinology, The Canberra Hospital, Canberra, Australian Capital Territory, Australia
  • Rakesh M Iyer
    Department of Endocrinology, The Canberra Hospital, Canberra, Australian Capital Territory, Australia
  • Caitlin E Coombes
    Australian National University Medical School, Australian National University, Canberra, Australian Capital Territory, Australia
  • Veronica Cheung
    Australian National University Medical School, Australian National University, Canberra, Australian Capital Territory, Australia
  • Melody Chiou
    Australian National University Medical School, Australian National University, Canberra, Australian Capital Territory, Australia
  • Ted Maddess
    Eccles Institute for Neuroscience, Australian National University, Canberra, Australian Capital Territory, Australia
  • Footnotes
    Commercial Relationships   Faran Sabeti, None; Corinne Carle, NuCoria (P); Christopher Nolan, None; Alicia Jenkins, None; Rohan Essex, None; Lauren Baker, None; Rakesh Iyer, None; Caitlin Coombes, None; Veronica Cheung, None; Melody Chiou, None; Ted Maddess, NuCoria (P), NuCoria (F), NuCoria (C)
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science July 2018, Vol.59, 1893. doi:
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      Faran Sabeti, Corinne F Carle, Christopher Nolan, Alicia Jenkins, Rohan Essex, Lauren Baker, Rakesh M Iyer, Caitlin E Coombes, Veronica Cheung, Melody Chiou, Ted Maddess; Changes in Macular function with Multifocal Pupillography and its spatial correlation with severity of Diabetic Retinopathy. Invest. Ophthalmol. Vis. Sci. 2018;59(9):1893.

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

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Abstract

Purpose : We compared the relationship between central retinal structure, and central retinal function as assessed multifocal pupillographic objective perimetry (mfPOP), in patients with Type 1 and Type 2 diabetes.

Methods : Pupillary responses were measured in thirty patients without retinopathy and thirty patients with retinopathy (25 with Type 1 diabetes, aged 52.7 ± 15.8 y; 35 with Type 2 diabetes, 61.6 ± 10.9 yr), and 43 age-matched controls (61.2 ± 9.3 y). mfPOP response amplitudes and delays within the central 30° of fixation were compared to the spatially corresponding full retinal thickness regions in the Early Treatment Diabetic Retinopathy Study (ETDRS) zones measured with optical coherence tomography (OCT). Correlation between groups were examined using Pearson’s Correlation Coefficients and differences were examined using t-tests.

Results : The results showed that there was no significant difference in central retinal thickness, retinal nerve fiber layer (RNFL) thickness, or HbA1c for all subject groups. Patients with type 2 diabetes (T2D) and controls had similar response amplitudes. Patients with Type 1 diabetes (T1D) had significantly reduced response amplitudes compared to controls and T2D group (P < 0.001), and this functional loss increased with progression to retinopathy. Response delays were significantly greater in both T1D and T2D compared to controls. Local correlations between retinal thickness and mfPOP reached significance towards the borders of macula in both patient groups (P < 0.05).

Conclusions : Neuroretinal dysfunction measured by mfPOP amplitude loss and delays in T1D is worse than in T2D. A positive spatial correlation between retinal thickness and mfPOP responses in peripheral ETDRS regions in eyes with retinopathy might indicate that regions outside the central retina are more vulnerable in earlier stages of disease. These findings suggest that peripheral functional loss in eyes with good vision may identify optimal candidates for early treatment and closer monitoring.

This is an abstract that was submitted for the 2018 ARVO Annual Meeting, held in Honolulu, Hawaii, April 29 - May 3, 2018.

 

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