Alterations of retinal thickness measured by optical coherence tomography correlate with neurophysiological measures in diabetic polyneuropathy

Abstract Aims/Introduction Diabetic polyneuropathy (DPN) and diabetic retinopathy (DR) are traditionally regarded as microvascular complications. However, these complications may share similar neurodegenerative pathologies. Here we evaluate the correlations in the severity of DPN and changes in the...

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Main Authors: Yuichiro Yamada, Tatsuhito Himeno, Kotaro Tsuboi, Yuka Shibata, Miyuka Kawai, Yuriko Asada‐Yamada, Yusuke Hayashi, Emi Asano‐Hayami, Tomohide Hayami, Yuichiro Ishida, Yohei Ejima, Mikio Motegi, Saeko Asano, Makoto Kato, Eriko Nagao, Hiromi Nakai‐Shimoda, Takahiro Ishikawa, Yoshiaki Morishita, Masaki Kondo, Shin Tsunekawa, Yoshiro Kato, Takayuki Nakayama, Motohiro Kamei, Jiro Nakamura, Hideki Kamiya
Format: Article
Language:English
Published: Wiley 2021-08-01
Series:Journal of Diabetes Investigation
Subjects:
Online Access:https://doi.org/10.1111/jdi.13476
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language English
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author Yuichiro Yamada
Tatsuhito Himeno
Kotaro Tsuboi
Yuka Shibata
Miyuka Kawai
Yuriko Asada‐Yamada
Yusuke Hayashi
Emi Asano‐Hayami
Tomohide Hayami
Yuichiro Ishida
Yohei Ejima
Mikio Motegi
Saeko Asano
Makoto Kato
Eriko Nagao
Hiromi Nakai‐Shimoda
Takahiro Ishikawa
Yoshiaki Morishita
Masaki Kondo
Shin Tsunekawa
Yoshiro Kato
Takayuki Nakayama
Motohiro Kamei
Jiro Nakamura
Hideki Kamiya
spellingShingle Yuichiro Yamada
Tatsuhito Himeno
Kotaro Tsuboi
Yuka Shibata
Miyuka Kawai
Yuriko Asada‐Yamada
Yusuke Hayashi
Emi Asano‐Hayami
Tomohide Hayami
Yuichiro Ishida
Yohei Ejima
Mikio Motegi
Saeko Asano
Makoto Kato
Eriko Nagao
Hiromi Nakai‐Shimoda
Takahiro Ishikawa
Yoshiaki Morishita
Masaki Kondo
Shin Tsunekawa
Yoshiro Kato
Takayuki Nakayama
Motohiro Kamei
Jiro Nakamura
Hideki Kamiya
Alterations of retinal thickness measured by optical coherence tomography correlate with neurophysiological measures in diabetic polyneuropathy
Journal of Diabetes Investigation
Diabetic polyneuropathies
Neuroretina
author_facet Yuichiro Yamada
Tatsuhito Himeno
Kotaro Tsuboi
Yuka Shibata
Miyuka Kawai
Yuriko Asada‐Yamada
Yusuke Hayashi
Emi Asano‐Hayami
Tomohide Hayami
Yuichiro Ishida
Yohei Ejima
Mikio Motegi
Saeko Asano
Makoto Kato
Eriko Nagao
Hiromi Nakai‐Shimoda
Takahiro Ishikawa
Yoshiaki Morishita
Masaki Kondo
Shin Tsunekawa
Yoshiro Kato
Takayuki Nakayama
Motohiro Kamei
Jiro Nakamura
Hideki Kamiya
author_sort Yuichiro Yamada
title Alterations of retinal thickness measured by optical coherence tomography correlate with neurophysiological measures in diabetic polyneuropathy
title_short Alterations of retinal thickness measured by optical coherence tomography correlate with neurophysiological measures in diabetic polyneuropathy
title_full Alterations of retinal thickness measured by optical coherence tomography correlate with neurophysiological measures in diabetic polyneuropathy
title_fullStr Alterations of retinal thickness measured by optical coherence tomography correlate with neurophysiological measures in diabetic polyneuropathy
title_full_unstemmed Alterations of retinal thickness measured by optical coherence tomography correlate with neurophysiological measures in diabetic polyneuropathy
title_sort alterations of retinal thickness measured by optical coherence tomography correlate with neurophysiological measures in diabetic polyneuropathy
publisher Wiley
series Journal of Diabetes Investigation
issn 2040-1116
2040-1124
publishDate 2021-08-01
description Abstract Aims/Introduction Diabetic polyneuropathy (DPN) and diabetic retinopathy (DR) are traditionally regarded as microvascular complications. However, these complications may share similar neurodegenerative pathologies. Here we evaluate the correlations in the severity of DPN and changes in the thickness of neuroretinal layers to elucidate whether these complications exist at similar stages of progression. Materials and Methods A total of 43 patients with type 2 diabetes underwent a nerve conduction study (NCS), a macular optical coherence tomography, and a carotid artery ultrasound scan. Diabetic polyneuropathy was classified according to Baba’s classification using NCS. The retina was automatically segmented into four layers; ganglion cell complex (GCC), inner nuclear layer/outer plexiform layer (INL/OPL), outer nuclear layer/photoreceptor inner and outer segments, and retinal pigment epithelium (RPE). The thickness of each retinal layer was separately analyzed for the fovea and the parafovea. Results Fourteen patients were classified as having moderate to severe diabetic polyneuropathy. The thicknesses of the foveal and parafoveal INL/OPL increased in patients with diabetic polyneuropathy compared with patients without. The thickness of the parafoveal retinal pigment epithelium decreased in patients with diabetic polyneuropathy. The thinning of parafoveal ganglion cell complex and foveal and parafoveal retinal pigment epithelium were positively correlated with deterioration of nerve functions in the nerve conduction study, but the thickening of INL/OPL was positively correlated with the nerve function deterioration. The thinning of parafoveal ganglion cell complex and foveal retinal pigment epithelium were positively correlated with the thickening of the carotid intima‐media. Conclusions Depending on the progression of diabetic polyneuropathy, the ganglion cell complex and retinal pigment epithelium became thinner and the INL/OPL became thicker. These retinal changes might be noteworthy for pathological investigations and for the assessment of diabetic polyneuropathy and diabetic retinopathy.
topic Diabetic polyneuropathies
Neuroretina
url https://doi.org/10.1111/jdi.13476
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spelling doaj-1a93ea39dc48466fab085a903c5af8a02021-08-10T18:00:48ZengWileyJournal of Diabetes Investigation2040-11162040-11242021-08-011281430144110.1111/jdi.13476Alterations of retinal thickness measured by optical coherence tomography correlate with neurophysiological measures in diabetic polyneuropathyYuichiro Yamada0Tatsuhito Himeno1Kotaro Tsuboi2Yuka Shibata3Miyuka Kawai4Yuriko Asada‐Yamada5Yusuke Hayashi6Emi Asano‐Hayami7Tomohide Hayami8Yuichiro Ishida9Yohei Ejima10Mikio Motegi11Saeko Asano12Makoto Kato13Eriko Nagao14Hiromi Nakai‐Shimoda15Takahiro Ishikawa16Yoshiaki Morishita17Masaki Kondo18Shin Tsunekawa19Yoshiro Kato20Takayuki Nakayama21Motohiro Kamei22Jiro Nakamura23Hideki Kamiya24Division of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDepartment of Ophthalmology Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDepartment of Ophthalmology Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDepartment of Clinical Laboratory Aichi Medical University Hospital Nagakute JapanDepartment of Ophthalmology Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanDivision of Diabetes Department of Internal Medicine Aichi Medical University School of Medicine Nagakute JapanAbstract Aims/Introduction Diabetic polyneuropathy (DPN) and diabetic retinopathy (DR) are traditionally regarded as microvascular complications. However, these complications may share similar neurodegenerative pathologies. Here we evaluate the correlations in the severity of DPN and changes in the thickness of neuroretinal layers to elucidate whether these complications exist at similar stages of progression. Materials and Methods A total of 43 patients with type 2 diabetes underwent a nerve conduction study (NCS), a macular optical coherence tomography, and a carotid artery ultrasound scan. Diabetic polyneuropathy was classified according to Baba’s classification using NCS. The retina was automatically segmented into four layers; ganglion cell complex (GCC), inner nuclear layer/outer plexiform layer (INL/OPL), outer nuclear layer/photoreceptor inner and outer segments, and retinal pigment epithelium (RPE). The thickness of each retinal layer was separately analyzed for the fovea and the parafovea. Results Fourteen patients were classified as having moderate to severe diabetic polyneuropathy. The thicknesses of the foveal and parafoveal INL/OPL increased in patients with diabetic polyneuropathy compared with patients without. The thickness of the parafoveal retinal pigment epithelium decreased in patients with diabetic polyneuropathy. The thinning of parafoveal ganglion cell complex and foveal and parafoveal retinal pigment epithelium were positively correlated with deterioration of nerve functions in the nerve conduction study, but the thickening of INL/OPL was positively correlated with the nerve function deterioration. The thinning of parafoveal ganglion cell complex and foveal retinal pigment epithelium were positively correlated with the thickening of the carotid intima‐media. Conclusions Depending on the progression of diabetic polyneuropathy, the ganglion cell complex and retinal pigment epithelium became thinner and the INL/OPL became thicker. These retinal changes might be noteworthy for pathological investigations and for the assessment of diabetic polyneuropathy and diabetic retinopathy.https://doi.org/10.1111/jdi.13476Diabetic polyneuropathiesNeuroretina