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Neuroretinal dysfunction revealed by a flicker electroretinogram correlated with peripheral nerve dysfunction and parameters of atherosclerosis in patients with diabetes
Aims/Introduction Diabetic polyneuropathy (DPN) develops in the early stage of diabetes. However, no common diagnostic protocol has yet been established. Here, to verify that the flicker electroretinogram using a hand‐held device can detect the early dysfunction of the peripheral nervous system in p...
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Published in: | Journal of diabetes investigation 2021-07, Vol.12 (7), p.1236-1243 |
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container_title | Journal of diabetes investigation |
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creator | Kawai, Miyuka Himeno, Tatsuhito Shibata, Yuka Hirai, Nobuhiro Asada‐Yamada, Yuriko Asano‐Hayami, Emi Ejima, Yohei Kasagi, Rina Nagao, Eriko Sugiura‐Roth, Yukako Nakai‐Shimoda, Hiromi Nakayama, Takayuki Yamada, Yuichiro Ishikawa, Takahiro Morishita, Yoshiaki Kondo, Masaki Tsunekawa, Shin Kato, Yoshiro Nakamura, Jiro Kamiya, Hideki |
description | Aims/Introduction
Diabetic polyneuropathy (DPN) develops in the early stage of diabetes. However, no common diagnostic protocol has yet been established. Here, to verify that the flicker electroretinogram using a hand‐held device can detect the early dysfunction of the peripheral nervous system in patients with diabetes, we investigated the correlation between the progression of DPN and neuroretinal dysfunction.
Materials and Methods
In total, 184 participants with type 1 or 2 diabetes underwent a flicker electroretinogram (ERG) using a hand‐held device RETeval™ and nerve conduction study. Participants were also evaluated for intima‐media thickness, ankle‐brachial index, toe brachial index and brachial‐ankle pulse wave velocity. Parameters of the nerve conduction study were used to diagnose the severity according to Baba’s classification. A multiple regression analysis was used to examine the associations of ERG parameters with the severity of DPN categorized by Baba’s classification. Diagnostic properties of the device in DPN were evaluated using a receiver operating characteristic curve.
Results
A multiple regression model to predict the severity of DPN was generated using ERG. In the model, moderate‐to‐severe DPN was effectively diagnosed (area under the receiver operating characteristic curve 0.692, sensitivity 56.5%, specificity 78.3%, positive predictive value 70.6%, negative predictive value 66.1%, positive likelihood ratio 2.60, negative likelihood ratio 0.56). In the patients without diabetic retinopathy, the implicit time and amplitude in ERG significantly correlated with the parameters of the nerve conduction study, brachial‐ankle pulse wave velocity and intima‐media thickness.
Conclusions
Electroretinogram parameters obtained by the hand‐held device successfully predict the severity of DPN. The device might be useful to evaluate DPN.
The progression of diabetic retinopathy and the dysfunction of neuroretina evaluated using the mydriasis‐free flicker electroretinogram showed a significant correlation. In patients without apparent diabetic retinopathy, the electroretinogram data correlated with parameters indicating vascular dysfunction, and with parameters indicating diabetic polyneuropathy, such as data of a nerve conduction study. Therefore, the electroretinogram data might reflect the neural and vascular impairments of the retina in patients with diabetes. The electroretinogram data were able to be used to predict the severity of diabetic pol |
doi_str_mv | 10.1111/jdi.13465 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_3b8f3a3ac5c64e48bf87eb0a12fb2cb7</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_3b8f3a3ac5c64e48bf87eb0a12fb2cb7</doaj_id><sourcerecordid>2552762999</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5885-4905d7ac132ab22c4507b2abf07342700c1bcde87462f8dccd0bff43758733c3</originalsourceid><addsrcrecordid>eNqFkstuEzEUQEcIRKvQBT-ALLGBRVq_ZsbZIKG2QFAFm-4tP64Th8k42J5U-ST-sm4mRAQJ4YVt2cfHvr63ql4TfElKu1pZf0kYb-pn1TnFHE8Jofz5cU6as-oipRUujQnRNO3L6owxSrBg9Xn16xsMMUTIvlcdsrvkht5kH3oUYQuqA4v0DinkOm9-QETQgcmHA2ER1RqZECN0Khfywecl2kD0myXEoushbuFEqnqLNqocgwwxoeCQyoUNyXRPvU_I9wXIHvqcRp_1Shc6vapeONUluDiMk-r-0-399Zfp3ffP8-uPd1NTC1FP-QzXtlWGMKo0pYbXuNVl6nDLOG0xNkQbC6LlDXXCGmOxdo6zthYtY4ZNqvmotUGt5Cb6tYo7GZSX-4UQF1LF7Mt7JdPCMcWUqU3DgQvtRAsaK0Kdpka3xfVhdG0GvQZrSlDlW06kpzu9X8pF2EpBG85LvibVu4Mghp8DpCzXPhnoOtVDGJKkJQhOCOezgr79C12FIZakFqquadvQ2ew_FJ8RSun-2vcjZUpOUgR3fDLB8qnoZCk6uS-6wr75M8Yj-bvECnA1Ag--g92_TfLrzXxUPgKFauWy</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2549122200</pqid></control><display><type>article</type><title>Neuroretinal dysfunction revealed by a flicker electroretinogram correlated with peripheral nerve dysfunction and parameters of atherosclerosis in patients with diabetes</title><source>Wiley-Blackwell Open Access Collection</source><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Kawai, Miyuka ; Himeno, Tatsuhito ; Shibata, Yuka ; Hirai, Nobuhiro ; Asada‐Yamada, Yuriko ; Asano‐Hayami, Emi ; Ejima, Yohei ; Kasagi, Rina ; Nagao, Eriko ; Sugiura‐Roth, Yukako ; Nakai‐Shimoda, Hiromi ; Nakayama, Takayuki ; Yamada, Yuichiro ; Ishikawa, Takahiro ; Morishita, Yoshiaki ; Kondo, Masaki ; Tsunekawa, Shin ; Kato, Yoshiro ; Nakamura, Jiro ; Kamiya, Hideki</creator><creatorcontrib>Kawai, Miyuka ; Himeno, Tatsuhito ; Shibata, Yuka ; Hirai, Nobuhiro ; Asada‐Yamada, Yuriko ; Asano‐Hayami, Emi ; Ejima, Yohei ; Kasagi, Rina ; Nagao, Eriko ; Sugiura‐Roth, Yukako ; Nakai‐Shimoda, Hiromi ; Nakayama, Takayuki ; Yamada, Yuichiro ; Ishikawa, Takahiro ; Morishita, Yoshiaki ; Kondo, Masaki ; Tsunekawa, Shin ; Kato, Yoshiro ; Nakamura, Jiro ; Kamiya, Hideki</creatorcontrib><description>Aims/Introduction
Diabetic polyneuropathy (DPN) develops in the early stage of diabetes. However, no common diagnostic protocol has yet been established. Here, to verify that the flicker electroretinogram using a hand‐held device can detect the early dysfunction of the peripheral nervous system in patients with diabetes, we investigated the correlation between the progression of DPN and neuroretinal dysfunction.
Materials and Methods
In total, 184 participants with type 1 or 2 diabetes underwent a flicker electroretinogram (ERG) using a hand‐held device RETeval™ and nerve conduction study. Participants were also evaluated for intima‐media thickness, ankle‐brachial index, toe brachial index and brachial‐ankle pulse wave velocity. Parameters of the nerve conduction study were used to diagnose the severity according to Baba’s classification. A multiple regression analysis was used to examine the associations of ERG parameters with the severity of DPN categorized by Baba’s classification. Diagnostic properties of the device in DPN were evaluated using a receiver operating characteristic curve.
Results
A multiple regression model to predict the severity of DPN was generated using ERG. In the model, moderate‐to‐severe DPN was effectively diagnosed (area under the receiver operating characteristic curve 0.692, sensitivity 56.5%, specificity 78.3%, positive predictive value 70.6%, negative predictive value 66.1%, positive likelihood ratio 2.60, negative likelihood ratio 0.56). In the patients without diabetic retinopathy, the implicit time and amplitude in ERG significantly correlated with the parameters of the nerve conduction study, brachial‐ankle pulse wave velocity and intima‐media thickness.
Conclusions
Electroretinogram parameters obtained by the hand‐held device successfully predict the severity of DPN. The device might be useful to evaluate DPN.
The progression of diabetic retinopathy and the dysfunction of neuroretina evaluated using the mydriasis‐free flicker electroretinogram showed a significant correlation. In patients without apparent diabetic retinopathy, the electroretinogram data correlated with parameters indicating vascular dysfunction, and with parameters indicating diabetic polyneuropathy, such as data of a nerve conduction study. Therefore, the electroretinogram data might reflect the neural and vascular impairments of the retina in patients with diabetes. The electroretinogram data were able to be used to predict the severity of diabetic polyneuropathy.</description><identifier>ISSN: 2040-1116</identifier><identifier>EISSN: 2040-1124</identifier><identifier>DOI: 10.1111/jdi.13465</identifier><identifier>PMID: 33210835</identifier><language>eng</language><publisher>Japan: John Wiley & Sons, Inc</publisher><subject>Aged ; Ankle ; Ankle Brachial Index ; Arteriosclerosis ; Atherosclerosis ; Atherosclerosis - complications ; Atherosclerosis - physiopathology ; Carotid Intima-Media Thickness ; Classification ; Creatinine ; Diabetes ; Diabetes mellitus (insulin dependent) ; Diabetes Mellitus, Type 1 - complications ; Diabetes Mellitus, Type 1 - physiopathology ; Diabetes Mellitus, Type 2 - complications ; Diabetes Mellitus, Type 2 - physiopathology ; Diabetic neuropathies ; Diabetic Neuropathies - diagnosis ; Diabetic Neuropathies - etiology ; Diabetic neuropathy ; Diabetic retinopathy ; Diabetic Retinopathy - diagnosis ; Diabetic Retinopathy - etiology ; Edema ; Electroretinography ; Electroretinography - instrumentation ; Electroretinography - methods ; Female ; Humans ; Kinases ; Laboratories ; Male ; Medical personnel ; Middle Aged ; Multiple regression analysis ; Nerve conduction ; Nervous system ; Neural Conduction - physiology ; Original ; Patients ; Peripheral nerves ; Peripheral Nerves - physiopathology ; Point‐of‐care testing ; Polyneuropathy ; Predictive Value of Tests ; Pulse Wave Analysis ; Retinopathy ; ROC Curve ; Severity of Illness Index ; Skin ; Velocity</subject><ispartof>Journal of diabetes investigation, 2021-07, Vol.12 (7), p.1236-1243</ispartof><rights>2020 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd</rights><rights>2020 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd.</rights><rights>2021. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5885-4905d7ac132ab22c4507b2abf07342700c1bcde87462f8dccd0bff43758733c3</cites><orcidid>0000-0003-0558-3404 ; 0000-0002-5677-1125 ; 0000-0002-3008-292X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2552762999/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2552762999?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,883,11549,25740,27911,27912,36999,37000,44577,46039,46463,53778,53780,74881</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33210835$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kawai, Miyuka</creatorcontrib><creatorcontrib>Himeno, Tatsuhito</creatorcontrib><creatorcontrib>Shibata, Yuka</creatorcontrib><creatorcontrib>Hirai, Nobuhiro</creatorcontrib><creatorcontrib>Asada‐Yamada, Yuriko</creatorcontrib><creatorcontrib>Asano‐Hayami, Emi</creatorcontrib><creatorcontrib>Ejima, Yohei</creatorcontrib><creatorcontrib>Kasagi, Rina</creatorcontrib><creatorcontrib>Nagao, Eriko</creatorcontrib><creatorcontrib>Sugiura‐Roth, Yukako</creatorcontrib><creatorcontrib>Nakai‐Shimoda, Hiromi</creatorcontrib><creatorcontrib>Nakayama, Takayuki</creatorcontrib><creatorcontrib>Yamada, Yuichiro</creatorcontrib><creatorcontrib>Ishikawa, Takahiro</creatorcontrib><creatorcontrib>Morishita, Yoshiaki</creatorcontrib><creatorcontrib>Kondo, Masaki</creatorcontrib><creatorcontrib>Tsunekawa, Shin</creatorcontrib><creatorcontrib>Kato, Yoshiro</creatorcontrib><creatorcontrib>Nakamura, Jiro</creatorcontrib><creatorcontrib>Kamiya, Hideki</creatorcontrib><title>Neuroretinal dysfunction revealed by a flicker electroretinogram correlated with peripheral nerve dysfunction and parameters of atherosclerosis in patients with diabetes</title><title>Journal of diabetes investigation</title><addtitle>J Diabetes Investig</addtitle><description>Aims/Introduction
Diabetic polyneuropathy (DPN) develops in the early stage of diabetes. However, no common diagnostic protocol has yet been established. Here, to verify that the flicker electroretinogram using a hand‐held device can detect the early dysfunction of the peripheral nervous system in patients with diabetes, we investigated the correlation between the progression of DPN and neuroretinal dysfunction.
Materials and Methods
In total, 184 participants with type 1 or 2 diabetes underwent a flicker electroretinogram (ERG) using a hand‐held device RETeval™ and nerve conduction study. Participants were also evaluated for intima‐media thickness, ankle‐brachial index, toe brachial index and brachial‐ankle pulse wave velocity. Parameters of the nerve conduction study were used to diagnose the severity according to Baba’s classification. A multiple regression analysis was used to examine the associations of ERG parameters with the severity of DPN categorized by Baba’s classification. Diagnostic properties of the device in DPN were evaluated using a receiver operating characteristic curve.
Results
A multiple regression model to predict the severity of DPN was generated using ERG. In the model, moderate‐to‐severe DPN was effectively diagnosed (area under the receiver operating characteristic curve 0.692, sensitivity 56.5%, specificity 78.3%, positive predictive value 70.6%, negative predictive value 66.1%, positive likelihood ratio 2.60, negative likelihood ratio 0.56). In the patients without diabetic retinopathy, the implicit time and amplitude in ERG significantly correlated with the parameters of the nerve conduction study, brachial‐ankle pulse wave velocity and intima‐media thickness.
Conclusions
Electroretinogram parameters obtained by the hand‐held device successfully predict the severity of DPN. The device might be useful to evaluate DPN.
The progression of diabetic retinopathy and the dysfunction of neuroretina evaluated using the mydriasis‐free flicker electroretinogram showed a significant correlation. In patients without apparent diabetic retinopathy, the electroretinogram data correlated with parameters indicating vascular dysfunction, and with parameters indicating diabetic polyneuropathy, such as data of a nerve conduction study. Therefore, the electroretinogram data might reflect the neural and vascular impairments of the retina in patients with diabetes. The electroretinogram data were able to be used to predict the severity of diabetic polyneuropathy.</description><subject>Aged</subject><subject>Ankle</subject><subject>Ankle Brachial Index</subject><subject>Arteriosclerosis</subject><subject>Atherosclerosis</subject><subject>Atherosclerosis - complications</subject><subject>Atherosclerosis - physiopathology</subject><subject>Carotid Intima-Media Thickness</subject><subject>Classification</subject><subject>Creatinine</subject><subject>Diabetes</subject><subject>Diabetes mellitus (insulin dependent)</subject><subject>Diabetes Mellitus, Type 1 - complications</subject><subject>Diabetes Mellitus, Type 1 - physiopathology</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>Diabetes Mellitus, Type 2 - physiopathology</subject><subject>Diabetic neuropathies</subject><subject>Diabetic Neuropathies - diagnosis</subject><subject>Diabetic Neuropathies - etiology</subject><subject>Diabetic neuropathy</subject><subject>Diabetic retinopathy</subject><subject>Diabetic Retinopathy - diagnosis</subject><subject>Diabetic Retinopathy - etiology</subject><subject>Edema</subject><subject>Electroretinography</subject><subject>Electroretinography - instrumentation</subject><subject>Electroretinography - methods</subject><subject>Female</subject><subject>Humans</subject><subject>Kinases</subject><subject>Laboratories</subject><subject>Male</subject><subject>Medical personnel</subject><subject>Middle Aged</subject><subject>Multiple regression analysis</subject><subject>Nerve conduction</subject><subject>Nervous system</subject><subject>Neural Conduction - physiology</subject><subject>Original</subject><subject>Patients</subject><subject>Peripheral nerves</subject><subject>Peripheral Nerves - physiopathology</subject><subject>Point‐of‐care testing</subject><subject>Polyneuropathy</subject><subject>Predictive Value of Tests</subject><subject>Pulse Wave Analysis</subject><subject>Retinopathy</subject><subject>ROC Curve</subject><subject>Severity of Illness Index</subject><subject>Skin</subject><subject>Velocity</subject><issn>2040-1116</issn><issn>2040-1124</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqFkstuEzEUQEcIRKvQBT-ALLGBRVq_ZsbZIKG2QFAFm-4tP64Th8k42J5U-ST-sm4mRAQJ4YVt2cfHvr63ql4TfElKu1pZf0kYb-pn1TnFHE8Jofz5cU6as-oipRUujQnRNO3L6owxSrBg9Xn16xsMMUTIvlcdsrvkht5kH3oUYQuqA4v0DinkOm9-QETQgcmHA2ER1RqZECN0Khfywecl2kD0myXEoushbuFEqnqLNqocgwwxoeCQyoUNyXRPvU_I9wXIHvqcRp_1Shc6vapeONUluDiMk-r-0-399Zfp3ffP8-uPd1NTC1FP-QzXtlWGMKo0pYbXuNVl6nDLOG0xNkQbC6LlDXXCGmOxdo6zthYtY4ZNqvmotUGt5Cb6tYo7GZSX-4UQF1LF7Mt7JdPCMcWUqU3DgQvtRAsaK0Kdpka3xfVhdG0GvQZrSlDlW06kpzu9X8pF2EpBG85LvibVu4Mghp8DpCzXPhnoOtVDGJKkJQhOCOezgr79C12FIZakFqquadvQ2ew_FJ8RSun-2vcjZUpOUgR3fDLB8qnoZCk6uS-6wr75M8Yj-bvECnA1Ag--g92_TfLrzXxUPgKFauWy</recordid><startdate>202107</startdate><enddate>202107</enddate><creator>Kawai, Miyuka</creator><creator>Himeno, Tatsuhito</creator><creator>Shibata, Yuka</creator><creator>Hirai, Nobuhiro</creator><creator>Asada‐Yamada, Yuriko</creator><creator>Asano‐Hayami, Emi</creator><creator>Ejima, Yohei</creator><creator>Kasagi, Rina</creator><creator>Nagao, Eriko</creator><creator>Sugiura‐Roth, Yukako</creator><creator>Nakai‐Shimoda, Hiromi</creator><creator>Nakayama, Takayuki</creator><creator>Yamada, Yuichiro</creator><creator>Ishikawa, Takahiro</creator><creator>Morishita, Yoshiaki</creator><creator>Kondo, Masaki</creator><creator>Tsunekawa, Shin</creator><creator>Kato, Yoshiro</creator><creator>Nakamura, Jiro</creator><creator>Kamiya, Hideki</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-0558-3404</orcidid><orcidid>https://orcid.org/0000-0002-5677-1125</orcidid><orcidid>https://orcid.org/0000-0002-3008-292X</orcidid></search><sort><creationdate>202107</creationdate><title>Neuroretinal dysfunction revealed by a flicker electroretinogram correlated with peripheral nerve dysfunction and parameters of atherosclerosis in patients with diabetes</title><author>Kawai, Miyuka ; Himeno, Tatsuhito ; Shibata, Yuka ; Hirai, Nobuhiro ; Asada‐Yamada, Yuriko ; Asano‐Hayami, Emi ; Ejima, Yohei ; Kasagi, Rina ; Nagao, Eriko ; Sugiura‐Roth, Yukako ; Nakai‐Shimoda, Hiromi ; Nakayama, Takayuki ; Yamada, Yuichiro ; Ishikawa, Takahiro ; Morishita, Yoshiaki ; Kondo, Masaki ; Tsunekawa, Shin ; Kato, Yoshiro ; Nakamura, Jiro ; Kamiya, Hideki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5885-4905d7ac132ab22c4507b2abf07342700c1bcde87462f8dccd0bff43758733c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Aged</topic><topic>Ankle</topic><topic>Ankle Brachial Index</topic><topic>Arteriosclerosis</topic><topic>Atherosclerosis</topic><topic>Atherosclerosis - complications</topic><topic>Atherosclerosis - physiopathology</topic><topic>Carotid Intima-Media Thickness</topic><topic>Classification</topic><topic>Creatinine</topic><topic>Diabetes</topic><topic>Diabetes mellitus (insulin dependent)</topic><topic>Diabetes Mellitus, Type 1 - complications</topic><topic>Diabetes Mellitus, Type 1 - physiopathology</topic><topic>Diabetes Mellitus, Type 2 - complications</topic><topic>Diabetes Mellitus, Type 2 - physiopathology</topic><topic>Diabetic neuropathies</topic><topic>Diabetic Neuropathies - diagnosis</topic><topic>Diabetic Neuropathies - etiology</topic><topic>Diabetic neuropathy</topic><topic>Diabetic retinopathy</topic><topic>Diabetic Retinopathy - diagnosis</topic><topic>Diabetic Retinopathy - etiology</topic><topic>Edema</topic><topic>Electroretinography</topic><topic>Electroretinography - instrumentation</topic><topic>Electroretinography - methods</topic><topic>Female</topic><topic>Humans</topic><topic>Kinases</topic><topic>Laboratories</topic><topic>Male</topic><topic>Medical personnel</topic><topic>Middle Aged</topic><topic>Multiple regression analysis</topic><topic>Nerve conduction</topic><topic>Nervous system</topic><topic>Neural Conduction - physiology</topic><topic>Original</topic><topic>Patients</topic><topic>Peripheral nerves</topic><topic>Peripheral Nerves - physiopathology</topic><topic>Point‐of‐care testing</topic><topic>Polyneuropathy</topic><topic>Predictive Value of Tests</topic><topic>Pulse Wave Analysis</topic><topic>Retinopathy</topic><topic>ROC Curve</topic><topic>Severity of Illness Index</topic><topic>Skin</topic><topic>Velocity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kawai, Miyuka</creatorcontrib><creatorcontrib>Himeno, Tatsuhito</creatorcontrib><creatorcontrib>Shibata, Yuka</creatorcontrib><creatorcontrib>Hirai, Nobuhiro</creatorcontrib><creatorcontrib>Asada‐Yamada, Yuriko</creatorcontrib><creatorcontrib>Asano‐Hayami, Emi</creatorcontrib><creatorcontrib>Ejima, Yohei</creatorcontrib><creatorcontrib>Kasagi, Rina</creatorcontrib><creatorcontrib>Nagao, Eriko</creatorcontrib><creatorcontrib>Sugiura‐Roth, Yukako</creatorcontrib><creatorcontrib>Nakai‐Shimoda, Hiromi</creatorcontrib><creatorcontrib>Nakayama, Takayuki</creatorcontrib><creatorcontrib>Yamada, Yuichiro</creatorcontrib><creatorcontrib>Ishikawa, Takahiro</creatorcontrib><creatorcontrib>Morishita, Yoshiaki</creatorcontrib><creatorcontrib>Kondo, Masaki</creatorcontrib><creatorcontrib>Tsunekawa, Shin</creatorcontrib><creatorcontrib>Kato, Yoshiro</creatorcontrib><creatorcontrib>Nakamura, Jiro</creatorcontrib><creatorcontrib>Kamiya, Hideki</creatorcontrib><collection>Wiley-Blackwell Open Access Collection</collection><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of diabetes investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kawai, Miyuka</au><au>Himeno, Tatsuhito</au><au>Shibata, Yuka</au><au>Hirai, Nobuhiro</au><au>Asada‐Yamada, Yuriko</au><au>Asano‐Hayami, Emi</au><au>Ejima, Yohei</au><au>Kasagi, Rina</au><au>Nagao, Eriko</au><au>Sugiura‐Roth, Yukako</au><au>Nakai‐Shimoda, Hiromi</au><au>Nakayama, Takayuki</au><au>Yamada, Yuichiro</au><au>Ishikawa, Takahiro</au><au>Morishita, Yoshiaki</au><au>Kondo, Masaki</au><au>Tsunekawa, Shin</au><au>Kato, Yoshiro</au><au>Nakamura, Jiro</au><au>Kamiya, Hideki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neuroretinal dysfunction revealed by a flicker electroretinogram correlated with peripheral nerve dysfunction and parameters of atherosclerosis in patients with diabetes</atitle><jtitle>Journal of diabetes investigation</jtitle><addtitle>J Diabetes Investig</addtitle><date>2021-07</date><risdate>2021</risdate><volume>12</volume><issue>7</issue><spage>1236</spage><epage>1243</epage><pages>1236-1243</pages><issn>2040-1116</issn><eissn>2040-1124</eissn><abstract>Aims/Introduction
Diabetic polyneuropathy (DPN) develops in the early stage of diabetes. However, no common diagnostic protocol has yet been established. Here, to verify that the flicker electroretinogram using a hand‐held device can detect the early dysfunction of the peripheral nervous system in patients with diabetes, we investigated the correlation between the progression of DPN and neuroretinal dysfunction.
Materials and Methods
In total, 184 participants with type 1 or 2 diabetes underwent a flicker electroretinogram (ERG) using a hand‐held device RETeval™ and nerve conduction study. Participants were also evaluated for intima‐media thickness, ankle‐brachial index, toe brachial index and brachial‐ankle pulse wave velocity. Parameters of the nerve conduction study were used to diagnose the severity according to Baba’s classification. A multiple regression analysis was used to examine the associations of ERG parameters with the severity of DPN categorized by Baba’s classification. Diagnostic properties of the device in DPN were evaluated using a receiver operating characteristic curve.
Results
A multiple regression model to predict the severity of DPN was generated using ERG. In the model, moderate‐to‐severe DPN was effectively diagnosed (area under the receiver operating characteristic curve 0.692, sensitivity 56.5%, specificity 78.3%, positive predictive value 70.6%, negative predictive value 66.1%, positive likelihood ratio 2.60, negative likelihood ratio 0.56). In the patients without diabetic retinopathy, the implicit time and amplitude in ERG significantly correlated with the parameters of the nerve conduction study, brachial‐ankle pulse wave velocity and intima‐media thickness.
Conclusions
Electroretinogram parameters obtained by the hand‐held device successfully predict the severity of DPN. The device might be useful to evaluate DPN.
The progression of diabetic retinopathy and the dysfunction of neuroretina evaluated using the mydriasis‐free flicker electroretinogram showed a significant correlation. In patients without apparent diabetic retinopathy, the electroretinogram data correlated with parameters indicating vascular dysfunction, and with parameters indicating diabetic polyneuropathy, such as data of a nerve conduction study. Therefore, the electroretinogram data might reflect the neural and vascular impairments of the retina in patients with diabetes. The electroretinogram data were able to be used to predict the severity of diabetic polyneuropathy.</abstract><cop>Japan</cop><pub>John Wiley & Sons, Inc</pub><pmid>33210835</pmid><doi>10.1111/jdi.13465</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-0558-3404</orcidid><orcidid>https://orcid.org/0000-0002-5677-1125</orcidid><orcidid>https://orcid.org/0000-0002-3008-292X</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2040-1116 |
ispartof | Journal of diabetes investigation, 2021-07, Vol.12 (7), p.1236-1243 |
issn | 2040-1116 2040-1124 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_3b8f3a3ac5c64e48bf87eb0a12fb2cb7 |
source | Wiley-Blackwell Open Access Collection; Publicly Available Content Database; PubMed Central |
subjects | Aged Ankle Ankle Brachial Index Arteriosclerosis Atherosclerosis Atherosclerosis - complications Atherosclerosis - physiopathology Carotid Intima-Media Thickness Classification Creatinine Diabetes Diabetes mellitus (insulin dependent) Diabetes Mellitus, Type 1 - complications Diabetes Mellitus, Type 1 - physiopathology Diabetes Mellitus, Type 2 - complications Diabetes Mellitus, Type 2 - physiopathology Diabetic neuropathies Diabetic Neuropathies - diagnosis Diabetic Neuropathies - etiology Diabetic neuropathy Diabetic retinopathy Diabetic Retinopathy - diagnosis Diabetic Retinopathy - etiology Edema Electroretinography Electroretinography - instrumentation Electroretinography - methods Female Humans Kinases Laboratories Male Medical personnel Middle Aged Multiple regression analysis Nerve conduction Nervous system Neural Conduction - physiology Original Patients Peripheral nerves Peripheral Nerves - physiopathology Point‐of‐care testing Polyneuropathy Predictive Value of Tests Pulse Wave Analysis Retinopathy ROC Curve Severity of Illness Index Skin Velocity |
title | Neuroretinal dysfunction revealed by a flicker electroretinogram correlated with peripheral nerve dysfunction and parameters of atherosclerosis in patients with diabetes |
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