In vivo characterization of ischemic retina in diabetic retinopathy

Lukas Reznicek, Marcus Kernt, Christos Haritoglou, Anselm Kampik, Michael Ulbig, Aljoscha S NeubauerDepartment of Ophthalmology, Ludwig Maximilian University, Munich, GermanyObjective: The aim of this article is to characterize pathomorphologic changes within particular layers of fluorescein angiogr...

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Autores principales: Lukas Reznicek, Marcus Kernt, Christos Haritoglou, et al
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Publicado: Dove Medical Press 2010
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spelling oai:doaj.org-article:4ad0be7212804c9181d6b6128d5deea22021-12-02T01:05:52ZIn vivo characterization of ischemic retina in diabetic retinopathy1177-54671177-5483https://doaj.org/article/4ad0be7212804c9181d6b6128d5deea22010-12-01T00:00:00Zhttp://www.dovepress.com/in-vivo-characterization-of-ischemic-retina-in-diabetic-retinopathy-a5983https://doaj.org/toc/1177-5467https://doaj.org/toc/1177-5483Lukas Reznicek, Marcus Kernt, Christos Haritoglou, Anselm Kampik, Michael Ulbig, Aljoscha S NeubauerDepartment of Ophthalmology, Ludwig Maximilian University, Munich, GermanyObjective: The aim of this article is to characterize pathomorphologic changes within particular layers of fluorescein angiographically 'ischemic' compared to 'nonischemic' retina in patients with diabetic retinopathy.Methods: Cross-sectional images of ischemic retinal areas were obtained using Heidelberg Spectralis optical coherence tomography (OCT). Presumed retinal ischemia was defined as focal hypofluorescence in early or early and late phase fluorescein angiography. Pathomorphologic changes on OCT were evaluated and the thickness of retinal layers measured and compared with nonischemic retina at corresponding topographic locations in a matched-pairs design based on 22 eyes (mean age 64 ± 14).Results: In all eyes, based on spectral domain-OCT cross-section images, the retina layers in ischemic retinal areas could be segmented. Total retinal thickness was significantly increased in ischemic compared to nonischemic areas (381 ± 94 µm versus 323 ± 89 µm, P = 0.005). Middle retinal layers (inner nuclear layer, outer plexiform layer, and outer nuclear layer) were significantly thickened in retinal ischemic areas (215 ± 82 µm versus 168 ± 62 µm, P = 0.002). The inner retinal layers (retinal nerve fiber layer, ganglion cell layer, and inner plexiform layer) showed a nonsignificant change (117 ± 53 µm versus 98 ± 30 µm), while the outer layers were slightly thinned (photoreceptors plus retinal pigment epithelium layer; 51 ± 9 µm versus 57 ± 8 µm, P = 0.02) in ischemic versus nonischemic retina.Conclusions: Ischemic diabetic retina seems to be thickened due to thickening of, in particular, middle retinal layers, which can be measured with high-resolution OCT.Keywords: OCT, Spectralis OCT, fluorescein angiography, diabetic retinopathy, ischemic retina, retinal thickness, retinal layers Lukas ReznicekMarcus KerntChristos Haritoglouet alDove Medical PressarticleOphthalmologyRE1-994ENClinical Ophthalmology, Vol 2011, Iss default, Pp 31-35 (2010)
institution DOAJ
collection DOAJ
language EN
topic Ophthalmology
RE1-994
spellingShingle Ophthalmology
RE1-994
Lukas Reznicek
Marcus Kernt
Christos Haritoglou
et al
In vivo characterization of ischemic retina in diabetic retinopathy
description Lukas Reznicek, Marcus Kernt, Christos Haritoglou, Anselm Kampik, Michael Ulbig, Aljoscha S NeubauerDepartment of Ophthalmology, Ludwig Maximilian University, Munich, GermanyObjective: The aim of this article is to characterize pathomorphologic changes within particular layers of fluorescein angiographically 'ischemic' compared to 'nonischemic' retina in patients with diabetic retinopathy.Methods: Cross-sectional images of ischemic retinal areas were obtained using Heidelberg Spectralis optical coherence tomography (OCT). Presumed retinal ischemia was defined as focal hypofluorescence in early or early and late phase fluorescein angiography. Pathomorphologic changes on OCT were evaluated and the thickness of retinal layers measured and compared with nonischemic retina at corresponding topographic locations in a matched-pairs design based on 22 eyes (mean age 64 ± 14).Results: In all eyes, based on spectral domain-OCT cross-section images, the retina layers in ischemic retinal areas could be segmented. Total retinal thickness was significantly increased in ischemic compared to nonischemic areas (381 ± 94 µm versus 323 ± 89 µm, P = 0.005). Middle retinal layers (inner nuclear layer, outer plexiform layer, and outer nuclear layer) were significantly thickened in retinal ischemic areas (215 ± 82 µm versus 168 ± 62 µm, P = 0.002). The inner retinal layers (retinal nerve fiber layer, ganglion cell layer, and inner plexiform layer) showed a nonsignificant change (117 ± 53 µm versus 98 ± 30 µm), while the outer layers were slightly thinned (photoreceptors plus retinal pigment epithelium layer; 51 ± 9 µm versus 57 ± 8 µm, P = 0.02) in ischemic versus nonischemic retina.Conclusions: Ischemic diabetic retina seems to be thickened due to thickening of, in particular, middle retinal layers, which can be measured with high-resolution OCT.Keywords: OCT, Spectralis OCT, fluorescein angiography, diabetic retinopathy, ischemic retina, retinal thickness, retinal layers
format article
author Lukas Reznicek
Marcus Kernt
Christos Haritoglou
et al
author_facet Lukas Reznicek
Marcus Kernt
Christos Haritoglou
et al
author_sort Lukas Reznicek
title In vivo characterization of ischemic retina in diabetic retinopathy
title_short In vivo characterization of ischemic retina in diabetic retinopathy
title_full In vivo characterization of ischemic retina in diabetic retinopathy
title_fullStr In vivo characterization of ischemic retina in diabetic retinopathy
title_full_unstemmed In vivo characterization of ischemic retina in diabetic retinopathy
title_sort in vivo characterization of ischemic retina in diabetic retinopathy
publisher Dove Medical Press
publishDate 2010
url https://doaj.org/article/4ad0be7212804c9181d6b6128d5deea2
work_keys_str_mv AT lukasreznicek invivocharacterizationofischemicretinaindiabeticretinopathy
AT marcuskernt invivocharacterizationofischemicretinaindiabeticretinopathy
AT christosharitoglou invivocharacterizationofischemicretinaindiabeticretinopathy
AT etal invivocharacterizationofischemicretinaindiabeticretinopathy
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