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Peripheral vision loss affects the processing of spatial frequencies in the central vision of people with glaucoma

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HAL Id: hal-01887270

https://hal.archives-ouvertes.fr/hal-01887270

Submitted on 3 Oct 2018

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Peripheral vision loss affects the processing of spatial frequencies in the central vision of people with glaucoma

Audrey Trouilloud, Alexia Roux-Sibilon, Floriane Rutgé, Louise Kauffmann, Arnaud Attye, Christophe Chiquet, Florent Aptel, Carole Peyrin

To cite this version:

Audrey Trouilloud, Alexia Roux-Sibilon, Floriane Rutgé, Louise Kauffmann, Arnaud Attye, et al..

Peripheral vision loss affects the processing of spatial frequencies in the central vision of people with

glaucoma. European Conference on Visual Perception, Aug 2018, Trieste, Italy. �hal-01887270�

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Introduction

Peripheral vision loss affects the processing of spatial frequencies in the central vision of people with glaucoma

Audrey Trouilloud

1

, Alexia Roux-Sibilon

1

, Floriane Rutgé

2,3

, Louise Kauffmann

1,4

, Arnaud Attyé

5,6

, Christophe Chiquet

2,3

, Florent Aptel

2,3

, and Carole Peyrin

1

This work was supported by University Grenoble Alpes PhD grant "AGIR-POLE-CBS » and by Fondation de France grant "Berthe Fouassier", https://www. fondationdefrance.org/fr/fondation/fondation- berthe-fouassier.

1 Univ. Grenoble Alpes, CNRS, LPNC, 38000 Grenoble, France

2 Department of Ophthalmology, Grenoble University Hospital, 38000 Grenoble, France 3 Univ. Grenoble Alpes, Inserm, CHU Grenoble Alpes, HP2, 38000 Grenoble, France 4 Univ. Grenoble Alpes, CNRS, Grenoble INP, GIPSA-Lab, 38000 Grenoble, France 5 Department of Neuroradiology and MRI, Grenoble University Hospital, 38000 Grenoble, France 6 Univ. Grenoble Alpes, Inserm US 17, CNRS UMS 3552, CHU Grenoble Alpes, IRMaGe, 38000 Grenoble, France

Glaucoma is an ocular disease characterized by a progressive destruction of the optic nerve and retinal ganglion cells (Fechtner & Weinreb, 1994).

This results in a progressive vision loss starting with a deficit in peripheral vision.

Retinal sensitivity loss impact more complex aspects of visual processing in patients with glaucoma, even early in the disease.

Patients reported having difficulty performing a wide range of daily activities, such as walking, reading or driving.

Behavioral experiments showed of visual deficits for global motion, global form, low-contrasted object and scene perception with stimuli displayed in the central vision of patients (Mc Kendrick et al., 2005; Lenoble et al., 2016; Roux-Sibilon et al., 2018).

These findings suggest a dysfunction on tasks mediated by parasol retinal ganglion cells (RGC), also called M cells sensitive to low luminance contrast, movements and more sensitive to low than high spatial frequencies.

Consistent with these findings, parasol RGC should be selectively damaged in early glaucoma (Quigley et al., 1988; see however Della Santina & Ou, 2017).

Aim: We assessed the spatial frequency processing in the central vision of glaucomatous patients during scene categorization, considering the progression of the disease.

Hypotheses: We expected a greater spatial frequency processing for LSF than for HSF at the early stage of the disease, and that advanced disease has a greater impact on HSF processing.

Method

Results

Conclusion

1 (OD) 2 (OG) 3 (OG) 4 (OD) 5 (OD) 6 (OD)

7 (OD) 8 (OG) 9 (OD) 10 (OG) 11 (OD) 12 (OG)

13 (OG) 14 (OG) 15 (OG) 16 (OG) 17 (OD) 18 (OD)

19 (OG) 20 (OD) 21 (OG) 22 (OG) 23 (OD) 24 (OG)

400 450 500 550 600 650 700 750 800 850

Control Early Non early Control Early Non early

Correct reaction times (ms)

Senstitivity index (d’)

0 0.5 1 1.5 2 2.5 3 3.5 4

Control Early Non early Control Early Non early 0

0.1 0.2 0.3 0.4 0.5 0.6 0.7

Control Early Non early Control Early Non early

Errors (%)

References

Della Santina, L., & Ou, Y. (2017). Who's lost first? Susceptibility of retinal ganglion cell types in experimental glaucoma. Exp Eye Res, 158, 43-50.

Fechtner, R. D., & Weinreb, R. N. (1994). Mechanisms of optic nerve damage in primary open angle glaucoma. Surv Ophthalmol, 39(1), 23-42.

Lenoble, Q., Lek, J. J., & McKendrick, A. M. (2016). Visual object categorisation in people with glaucoma. Br J Ophthalmol, 100(11), 1585-1590.

McKendrick, A. M., et al. (2005). The detection of both global motion and global form is disrupted in glaucoma. Invest Ophthalmol Vis Sci, 46(10), 3693-3701.

Quigley, H. A., & Broman, A. T. (2006). The number of people with glaucoma worldwide in 2010 and 2020. Br J Ophthalmol, 90(3), 262-267.

Roux-Sibilon, A., Rutgé, F., Aptel, F., Attye, A., Guyader, N., Boucart, M., Chiquet, C., & Peyrin, C. (2018). Scene and human face recognition in the central vision of patients with glaucoma. PLoS One, 13(2):e0193465.

Participants

- 24 patients with Primary Open Angle Glaucoma (POAG) - 22 age-matched control participants (67 years ± 5)

Patients were divided into two groups, based on the severity of the visual field (Humphreys Visual Field analyzer, 24-2 SITA-Standard)

Ø  12 patients with early glaucoma: Mean Deviation > -6 dB (68 years ± 9)

Ø 12 patients with non early glaucoma: Mean Deviation < -6 dB (70 years ± 10)

Stimuli

Indoor and outdoor scenes (6°x4° of visual angle) selected form ReCor Database. http://doi.org/10.17605/OSF.IO/XJDQ4 filtered in -  Low spatial frequencies (LSF; < 2 cpd or 12 cpi),

-  High spatial frequencies (HSF; >6 cpd or 36 cpi).

Luminance and contrast luminance contrast were normalized between LSF and HSF Luminance: 72 on a 256 grey level scale (0.28 for luminance value between 0 and 1)

RMS contrast: 33 on a 256 grey level scale (0.13 for luminance value between 0 and 1) è Contrast of 46%

Procedure

- Scenes were presented in the central visual field for 100 ms.

- Participants performed a categorization task (go/no-go response): they were instructed to press the keyboard spacebar whenever the scene appearing on the screen belonged to a target category (indoor or outdoor category; target category is counterbalanced across participants of each group).

- Each participant was tested monocularly (Near visual acuity: Parinaud < 2; Far visual acuity: > 7/10

e

).

LSF

HSF

6° of visual angle

of visual angle

500 ms 100 ms

38 cm

The global deficit for HSF processing could be linked to the functional decline of the parvocellular pathway in normal aging (Elliott & Werner, 2010).

Patients classified as having early visual field defect had a selective deficit for low-pass filtered scenes, in comparison to controls, while patients with a more severe glaucoma were impaired in all spatial frequencies.

A deficit for spatial frequency processing should appear sequentially as a function of the disease progression. The simple loss of peripheral vision could be detrimental to scene recognition in the relatively preserved central vision of patients. The deficits observed in central vision can be thought as a result of a trans-synaptic degeneration in glaucoma following the optic nerve damage and resulting in a disorganization of high-level visual cortical regions (e.g., Scene-selective parahippocampal place area, Epstein & Kanwisher, 1998).

Errors (%)

- group effect: Controls > Patients F(2,43) = 8.08, p < .001 - SF effect: LSF < HSF F(1,43) = 10.49, p < .001 - group*SF: F(2,43) = 3.43, p < .05

•  Control < Early on LSF F(1,43) = 4.11, p < .05,

•  No difference between Control and Early on HSF F(1,43) < 1

•  Control < Non early on LSF F(1,43) = 10.53, p < .01,

•  Control < Non early on HSF F(1,43) = 15.17 p < .001 - severity*SF: F(1,43) = 5,14, p < .05

•  no severity effect on LSF F(1,43) = 1.14, p = .29

•  severity effect on HSF: Early > Non early F(1,43) = 7.11, p < .01

Index of sensitivity (d’)

- group effect: Controls > Patients F(2,43) = 10,04, p < .001 - SF effect: LSF > HSF F(1,43) = 7,22, p < .01 - no group*SF: F(2,43) = 2.58, p = .08 - severity*SF: F(1,43) = 6.06, p < .05

•  no severity effect on LSF F(1,43) < 1

•  severity effect on HSF: Early > Non early F(1,43) = 7.36, p < .01

Correct reaction times (ms)

- no group effect F(2,43) < 1 - SF effect: LSF < HSF F(1,43) = 6.65, p < .01 - no group*SF effect F(2,43) < 1

*

LSF HSF LSF HSF LSF HSF

*

* *

*

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