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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Wiley
2021-08-01
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Series: | Journal of Diabetes Investigation |
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Online Access: | https://doi.org/10.1111/jdi.13476 |
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Article |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
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 |
work_keys_str_mv |
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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 |