Skip to main content
Top
Published in: Graefe's Archive for Clinical and Experimental Ophthalmology 9/2014

01-09-2014 | Neurophthalmology

Macular ganglion cell–inner plexiform layer thinning in patients with visual field defect that respects the vertical meridian

Authors: Hye-Young Shin, Hae-Young Lopilly Park, Jin-A Choi, Chan Kee Park

Published in: Graefe's Archive for Clinical and Experimental Ophthalmology | Issue 9/2014

Login to get access

Abstract

The aim of this work is to compare the thinning patterns of the ganglion cell inner-plexiform layer (GCIPL) and peripapillary retinal nerve fiber layer (pRNFL) as measured using Cirrus high-definition optical coherence tomography (HD-OCT) in patients with visual field (VF) defects that respect the vertical meridian. Twenty eyes of 11 patients with VF defects that respect the vertical meridian were enrolled retrospectively. The thicknesses of the macular GCIPL and pRNFL were measured using Cirrus HD-OCT. The 5 and 1 % thinning area index (TAI) was calculated as the proportion of abnormally thin sectors at the 5 and 1 % probability level within the area corresponding to the affected VF. The 5 and 1 % TAI were compared between the GCIPL and pRNFL measurements. The color-coded GCIPL deviation map showed a characteristic vertical thinning pattern of the GCIPL, which is also seen in the VF of patients with brain lesions. The 5 and 1 % TAI were significantly higher in the GCIPL measurements than in the pRNFL measurements (all p < 0.01). Macular GCIPL analysis clearly visualized a characteristic topographic pattern of retinal ganglion cell (RGC) loss in patients with VF defects that respect the vertical meridian, unlike pRNFL measurements. Macular GCIPL measurements provide more valuable information than pRNFL measurements for detecting the loss of RGCs in patients with retrograde degeneration of the optic nerve fibers.
Literature
1.
go back to reference Jindahra P, Petrie A, Plant GT (2012) The time course of retrograde trans-synaptic degeneration following occipital lobe damage in humans. Brain 135:534–541PubMedCrossRef Jindahra P, Petrie A, Plant GT (2012) The time course of retrograde trans-synaptic degeneration following occipital lobe damage in humans. Brain 135:534–541PubMedCrossRef
2.
go back to reference Jindahra P, Petrie A, Plant GT (2009) Retrograde trans-synaptic retinal ganglion cell loss identified by optical coherence tomography. Brain 132:628–634PubMedCrossRef Jindahra P, Petrie A, Plant GT (2009) Retrograde trans-synaptic retinal ganglion cell loss identified by optical coherence tomography. Brain 132:628–634PubMedCrossRef
3.
go back to reference Bridge H, Jindahra P, Barbur J, Plant GT (2011) Imaging reveals optic tract degeneration in hemianopia. Invest Ophthalmol Vis Sci 52:382–388PubMedCrossRef Bridge H, Jindahra P, Barbur J, Plant GT (2011) Imaging reveals optic tract degeneration in hemianopia. Invest Ophthalmol Vis Sci 52:382–388PubMedCrossRef
4.
go back to reference Cowey A, Alexander I, Stoerig P (2011) Transneuronal retrograde degeneration of retinal ganglion cells and optic tract in hemianopic monkeys and humans. Brain 134:2149–2157PubMedCrossRef Cowey A, Alexander I, Stoerig P (2011) Transneuronal retrograde degeneration of retinal ganglion cells and optic tract in hemianopic monkeys and humans. Brain 134:2149–2157PubMedCrossRef
5.
go back to reference Park HY, Park YG, Cho AH, Park CK (2013) Transneuronal retrograde degeneration of the retinal ganglion cells in patients with cerebral infarction. Ophthalmology 120:1292–1299PubMedCrossRef Park HY, Park YG, Cho AH, Park CK (2013) Transneuronal retrograde degeneration of the retinal ganglion cells in patients with cerebral infarction. Ophthalmology 120:1292–1299PubMedCrossRef
6.
go back to reference Tatsumi Y, Kanamori A, Kusuhara A, Nakanishi Y, Kusuhara S, Nakamura M (2005) Retinal nerve fiber layer thickness in optic tract syndrome. Jpn J Ophthalmol 49:294–296PubMedCrossRef Tatsumi Y, Kanamori A, Kusuhara A, Nakanishi Y, Kusuhara S, Nakamura M (2005) Retinal nerve fiber layer thickness in optic tract syndrome. Jpn J Ophthalmol 49:294–296PubMedCrossRef
7.
go back to reference Kanamori A, Nakamura M, Yamada Y, Negi A (2013) Spectral-domain optical coherence tomography detects optic atrophy due to optic tract syndrome. Graefes Arch Clin Exp Ophthalmol 251:591–595PubMedCrossRef Kanamori A, Nakamura M, Yamada Y, Negi A (2013) Spectral-domain optical coherence tomography detects optic atrophy due to optic tract syndrome. Graefes Arch Clin Exp Ophthalmol 251:591–595PubMedCrossRef
8.
go back to reference Yamashita T, Miki A, Iguchi Y, Kimura K, Maeda F, Kiryu J (2012) Reduced retinal ganglion cell complex thickness in patients with posterior cerebral artery infarction detected using spectral-domain optical coherence tomography. Jpn J Ophthalmol 56:502–510PubMedCrossRef Yamashita T, Miki A, Iguchi Y, Kimura K, Maeda F, Kiryu J (2012) Reduced retinal ganglion cell complex thickness in patients with posterior cerebral artery infarction detected using spectral-domain optical coherence tomography. Jpn J Ophthalmol 56:502–510PubMedCrossRef
9.
go back to reference Zhang X, Kedar S, Lynn MJ, Newman NJ, Biousse V (2006) Homonymous hemianopias: clinical-anatomic correlations in 904 cases. Neurology 66:906–910PubMedCrossRef Zhang X, Kedar S, Lynn MJ, Newman NJ, Biousse V (2006) Homonymous hemianopias: clinical-anatomic correlations in 904 cases. Neurology 66:906–910PubMedCrossRef
10.
go back to reference Newman SA, Miller NR (1983) Optic tract syndrome. Neuro-ophthalmologic considerations. Arch Ophthalmol 101:1241–1250PubMedCrossRef Newman SA, Miller NR (1983) Optic tract syndrome. Neuro-ophthalmologic considerations. Arch Ophthalmol 101:1241–1250PubMedCrossRef
11.
go back to reference Gilhotra JS (2002) Homonymous visual field defects and stroke in an older population. Stroke 33:2417–2420PubMedCrossRef Gilhotra JS (2002) Homonymous visual field defects and stroke in an older population. Stroke 33:2417–2420PubMedCrossRef
12.
go back to reference Mwanza JC, Oakley JD, Budenz DL, Chang RT, Knight OJ, Feuer WJ (2011) Macular ganglion cell–inner plexiform layer: automated detection and thickness reproducibility with spectral domain-optical coherence tomography in glaucoma. Invest Ophthalmol Vis Sci 52:8323–8329PubMedCentralPubMedCrossRef Mwanza JC, Oakley JD, Budenz DL, Chang RT, Knight OJ, Feuer WJ (2011) Macular ganglion cell–inner plexiform layer: automated detection and thickness reproducibility with spectral domain-optical coherence tomography in glaucoma. Invest Ophthalmol Vis Sci 52:8323–8329PubMedCentralPubMedCrossRef
13.
go back to reference Mwanza JC, Durbin MK, Budenz DL, Girkin CA, Leung CK, Liebmann JM, Peace JH, Werner JS, Wollstein G (2011) Profile and predictors of normal ganglion cell–inner plexiform layer thickness measured with frequency-domain optical coherence tomography. Invest Ophthalmol Vis Sci 52:7872–7879PubMedCrossRef Mwanza JC, Durbin MK, Budenz DL, Girkin CA, Leung CK, Liebmann JM, Peace JH, Werner JS, Wollstein G (2011) Profile and predictors of normal ganglion cell–inner plexiform layer thickness measured with frequency-domain optical coherence tomography. Invest Ophthalmol Vis Sci 52:7872–7879PubMedCrossRef
14.
Metadata
Title
Macular ganglion cell–inner plexiform layer thinning in patients with visual field defect that respects the vertical meridian
Authors
Hye-Young Shin
Hae-Young Lopilly Park
Jin-A Choi
Chan Kee Park
Publication date
01-09-2014
Publisher
Springer Berlin Heidelberg
Published in
Graefe's Archive for Clinical and Experimental Ophthalmology / Issue 9/2014
Print ISSN: 0721-832X
Electronic ISSN: 1435-702X
DOI
https://doi.org/10.1007/s00417-014-2706-3

Other articles of this Issue 9/2014

Graefe's Archive for Clinical and Experimental Ophthalmology 9/2014 Go to the issue