Retrospective evaluation of pre-surgical electroretinography results in a mixed-breed canine population presented for cataract removal surgery.


Journal

Veterinary ophthalmology
ISSN: 1463-5224
Titre abrégé: Vet Ophthalmol
Pays: England
ID NLM: 100887377

Informations de publication

Date de publication:
Mar 2023
Historique:
revised: 23 05 2022
received: 04 09 2021
accepted: 24 05 2022
medline: 31 3 2023
pubmed: 2 6 2022
entrez: 1 6 2022
Statut: ppublish

Résumé

Electroretinography (ERG) is used prior to cataract removal surgery to assess retinal function. We aimed to replicate and improve upon previous studies by performing a full ECVO protocol and by examining the retina post-surgery in all patients. One hundred twenty-seven eyes from 67 dogs were included in the study. A full ECVO protocol electroretinography, which includes extensive rod and cone analysis, was performed on all dogs presenting for cataract surgery. Our main findings were that amplitudes, but not implicit times of rod responses decreased with advanced cataracts. Amplitudes of the single flash rod and rod flicker responses were significantly lower in eyes with mature cataracts, and the former also decreased in hypermature cataracts. Cone flicker amplitude responses were also significantly lower in eyes with mature and hypermature cataracts. However, mixed single flash rod-cone and cone responses, with the exception of the mixed rod-cone a-wave amplitude in eyes with hypermature cataracts, were unaffected by cataract stage. The b-wave amplitude of the scotopic, mixed rod-cone, and photopic cone responses were affected by age and decreased by an average of 2.9, 7.5, and 1.5 μV/year, retrospectively (p < 0.01). Lower ERG amplitudes in canine cataract patients may result from aging or the presence of advanced cataracts and may not indicate the presence of retinal disease.

Identifiants

pubmed: 35649104
doi: 10.1111/vop.13001
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

145-154

Informations de copyright

© 2022 American College of Veterinary Ophthalmologists.

Références

Ofri R. Retina. In: Maggs DJ, Miller PE, Ofri R, eds. Slatter's Fundamentals of Veterinary Ophthalmology. 5th ed. Elsevier; 2013:299-333.
Ben-Shlomo G. Ophthalmic examination and diagnostics, part 4: clinical electrodiagnostic evaluation of the visual system. In: Gelatt KN, Gilger BC, Kern TJ, eds. Veterinary Ophthalmology. 6th ed. Wiley-Blackwell; 2021:757-777.
Pasmanter N, Petersen-Jones SM. A review of electroretinography waveforms and models and their application in the dog. Vet Ophthalmol. 2020;23(3):418-435. doi:10.1111/vop.12759
Narfström K, Ekesten B, Rosolen SG, Spiess BM, Percicot CL, Ofri R. Guidelines for clinical electroretinography in the dog. Doc Ophthalmol. 2002;105(2):83-92. doi:10.1023/a:1020524305726
Ekesten B, Komáromy AM, Ofri R, Petersen-Jones SM, Narfström K. Guidelines for clinical electroretinography in the dog: 2012 update. Doc Ophthalmol. 2013;127(2):79-87. doi:10.1007/s10633-013-9388-8
Petersen-Jones SM, Komáromy AM. Dog models for blinding inherited retinal dystrophies. Hum Gene Ther Clin Dev. 2015;26(1):15-26. doi:10.1089/humc.2014.155
Narfström KN, Petersen-Jones SM. Diseases of the canine ocular fundus. In: Gelatt KN, Gilger BC, Kern TJ, eds. Veterinary Ophthalmology. 5th ed. Wiley-Blackwell; 2013:1303-1392.
Ofri R. Diseases of the retina. In: Maggs DJ, Miller PE, Ofri R, eds. Slatter's Fundamentals of Veterinary Ophthalmology. 6th ed. Elsevier; 2018:347-389.
Aguirre GD, Rubin LF. The electrogram in dogs with inherited cone degeneration. Investig Ophthalmol. 1975;14(11):840-847.
Ezra-Elia R, Banin E, Honig H, et al. Flicker cone function in normal and day blind sheep: a large animal model for human achromatopsia caused by CNGA3 mutation. Doc Ophthalmol. 2014;129(3):141-150.
Kondo M, Das G, Imai R, et al. A naturally occurring canine model of autosomal recessive congenital stationary night blindness. PLoS One. 2015;10(9):e0137072.
Oh A, Loew ER, Foster ML, et al. Phenotypic characterization of complete CSNB in the inbred research beagle: how common is CSNB in research and companion dogs? Doc Ophthalmol. 2018;137(2):87-101. doi:10.1007/s10633-018-9653-y
Montgomery KW, van der Woerdt A, Cottrill NB. Acute blindness in dogs: sudden acquired retinal degeneration syndrome versus neurological disease (140 cases, 2000-2006). Vet Ophthalmol. 2008;11(5):314-320. doi:10.1111/j.1463-5224.2008.00652.x
Komáromy AM, Abrams KL, Heckenlively JR, et al. Sudden acquired retinal degeneration syndrome (SARDS) - a review and proposed strategies toward a better understanding of pathogenesis, early diagnosis, and therapy. Vet Ophthalmol. 2016;19(4):319-331. doi:10.1111/vop.12291
Hoffman A, Sisler S, Pappania M, Hsu K, Ross M, Ofri R. Electroretinography is a prognostic indicator for postoperative vision in dogs undergoing retinal reattachment surgery. Vet Ophthalmol. 2018;21(3):273-280. doi:10.1111/vop.12505
Wilkie DA, Colitz MHC. Surgery of the lens. In: Gelatt KN, Gilger BC, Kern TJ, eds. Veterinary Ophthalmology. 5th ed. Ames, Iowa; 2013:1234-1286.
Ofri R. Diseases of the lens. In: Maggs DJ, Miller PE, Ofri R, eds. Slatter's Fundamentals of Veterinary Ophthalmology. 6th ed. Elsevier; 2018:306-333.
Grozdanic SD, Kecova H, Lazic T. Rapid diagnosis of retina and optic nerve abnormalities in canine patients with and without cataracts using chromatic pupil light reflex testing. Vet Ophthalmol. 2013;16(5):329-340. doi:10.1111/vop.12003
Park AS, Yi NY, Jeong MB, et al. Clinical manifestations of cataracts in small breed dogs. Vet Ophthalmol. 2009;12(4):205-210. doi:10.1111/j.1463-5224.2009.00697.x
de Waard PW, Ijspeert JK, Van Den Berg TJ, De Jong PT. Intraocular light scattering in age-related cataracts. Invest Ophthalmol Vis Sci. 1992;33(3):618-625.
Moschos MM, Gouliopoulos NS, Kalogeropoulos C. Electrophysiological examination in uveitis: a review of the literature. Clin Ophthalmol. 2014;8:199-214. doi:10.2147/OPTH.S54838
Tuntivanich N, Mentzer AL, Eifler DM, et al. Assessment of the dark-adaptation time required for recovery of electroretinographic responses in dogs after fundus photography and indirect ophthalmoscopy. Am J Vet Res. 2005;66(10):1798-1804. doi:10.2460/ajvr.2005.66.1798
Kooijman AC, Damhof A. A tricolor light source for stimulation and adaptation in electroretinography. Doc Opthalmol. 1986;63:195-203.
Itoh Y, Maehara S, Itoh N, Yamashita K, Izumisawa Y. Electroretinography recordings using a light emitting diode active corneal electrode in healthy beagle dogs. J Vet Sci. 2013;14(1):77-84. doi:10.4142/jvs.2013.14.1.77
Sandalon S, Boykova A, Ross M, Obolensky A, Banin E, Ofri R. Contrary to popular belief, chinchillas do not have a pure rod retina. Vet Ophthalmol. 2019;22(1):93-97. doi:10.1111/vop.12581
Murray SJ, Russell KN, Melzer TR, et al. Intravitreal gene therapy protects against retinal dysfunction in sheep with CLN5 batten disease. Exp Eye Res. 2021;207:1-12. doi:10.1016/j.exer.2021.108600
Maehara S, Itoh N, Wakaiki S, Yamasaki A, Tsuzuki K, Izumisawa Y. The effects of cataract stage, lens-induced uveitis and cataract removal on ERG in dogs with cataract. Vet Ophthalmol. 2007;10(5):308-312. doi:10.1111/j.1463-5224.2007.00559.x
Cruz RD, Adachi-Usami E. Quantitative evaluation of electroretinogram before cataract surgery. Jpn J Ophthalmol. 1989;33(4):451-457.
Tanikawa A, Suzuki K, Nomura R, et al. The influence of mild cataract on ISCEV standard electroretinogram recorded from mydriatic eyes. Doc Ophthalmol. 2021;142(2):177-183. doi:10.1007/s10633-020-09791-y
Miura G, Sato E, Yamamoto S. Flicker electroretinograms recorded with mydriasis-free RETeval system before and after cataract surgery. Eye (Lond). 2017;31(11):1589-1593. doi:10.1038/eye.2017.110
Yamauchi Y, Mochizuki J-I, Hirakata A, Uda S. Single flash electroretinograms of mature cataractous and fellow eyes. Clin Ophthalmol. 2016;10:2031-2034. doi:10.2147/OPTH.S118677
Occelli LM, Pasmanter N, Ayoub EE, Petersen-Jones SM. Changes in retinal layer thickness with maturation in the dog: an in vivo spectral domain - optical coherence tomography imaging study. BMC Vet Res. 2020;16(1):225. doi:10.1186/s12917-020-02390-8
Ofri R, Ekesten B. Baseline retinal OCT measurements in normal female beagles: the effects of eccentricity, meridian, and age on retinal layer thickness. Vet Ophthalmol. 2020;23(1):52-60. doi:10.1111/vop.12683
Panda-Jonas S, Jonas JB, Jakobczyk-Zmija M. Retinal photoreceptor density decreases with age. Ophthalmology. 1995;102(12):1853-1859.
Curcio CA, Millican CL, Allen KA, Kalina RE. Aging of the human photoreceptor mosaic: evidence for selective vulnerability of rods in central retina. Invest Ophthalmol Vis Sci. 1993;34(12):3278-3296.
Aggarwal P, Nag TC, Wadhwa S. Age-related decrease in rod bipolar cell density of the human retina: an immunohistochemical study. J Biosci. 2007;32(2):293-298. doi:10.1007/s12038-007-0029-9
Balazsi AG, Rootman J, Drance SM, Schulzer M, Douglas GR. The effect of age on the nerve fiber population of the human optic nerve. Am J Ophthalmol. 1984;97(6):760-766. doi:10.1016/0002-9394(84)90509-9

Auteurs

Michaela L Wegg (ML)

The Roslin Institute, The University of Edinburgh, Midlothian, UK.

Danica Pollard (D)

The Rodhams, Wisbech, UK.

Ron Ofri (R)

Koret School of Veterinary Medicine, Hebrew University of Jerusalem, Rehovot, Israel.

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